---
_id: '10926'
abstract:
- lang: eng
  text: Conflict over reproduction between females and males exists because of anisogamy
    and promiscuity. Together they generate differences in fitness optima between
    the sexes and result in antagonistic coevolution of female and male reproductive
    traits. Mounting duration is likely to be a compromise between male and female
    interests whose outcome depends on the intensity of sexual selection. The timing
    of sperm transfer during mounting is critical. For example, mountings may be interrupted
    before sperm is transferred as a consequence of female or male choice, or they
    may be prolonged to function as mate guarding. In the highly promiscuous intertidal
    snail Littorina saxatilis, mountings vary substantially in duration, from less
    than a minute to more than an hour, and it has been assumed that mountings of
    a few minutes do not result in any sperm being transferred. Here, we examined
    the timing of sperm transfer, a reproductive trait that is likely affected by
    sexual conflict. We performed time-controlled mounting trials using L. saxatilis
    males and virgin females, aiming to examine indirectly when the transfer of sperm
    starts. We observed the relationship between mounting duration and the proportion
    of developing embryos out of all eggs and embryos in the brood pouch. Developing
    embryos were observed in similar proportions in all treatments (i.e. 1, 5 and
    10 or more minutes at which mountings were artificially interrupted), suggesting
    that sperm transfer begins rapidly (within 1 min) in L. saxatilis and very short
    matings do not result in sperm shortage in the females. We discuss how the observed
    pattern can be influenced by predation risk, population density, and female status
    and receptivity.
article_number: eyab049
article_processing_charge: No
article_type: original
author:
- first_name: Samuel
  full_name: Perini, Samuel
  last_name: Perini
- first_name: Rogerk
  full_name: Butlin, Rogerk
  last_name: Butlin
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: Kerstin
  full_name: Johannesson, Kerstin
  last_name: Johannesson
citation:
  ama: Perini S, Butlin R, Westram AM, Johannesson K. Very short mountings are enough
    for sperm transfer in Littorina saxatilis. <i>Journal of Molluscan Studies</i>.
    2022;88(1). doi:<a href="https://doi.org/10.1093/mollus/eyab049">10.1093/mollus/eyab049</a>
  apa: Perini, S., Butlin, R., Westram, A. M., &#38; Johannesson, K. (2022). Very
    short mountings are enough for sperm transfer in Littorina saxatilis. <i>Journal
    of Molluscan Studies</i>. Oxford Academic. <a href="https://doi.org/10.1093/mollus/eyab049">https://doi.org/10.1093/mollus/eyab049</a>
  chicago: Perini, Samuel, Rogerk Butlin, Anja M Westram, and Kerstin Johannesson.
    “Very Short Mountings Are Enough for Sperm Transfer in Littorina Saxatilis.” <i>Journal
    of Molluscan Studies</i>. Oxford Academic, 2022. <a href="https://doi.org/10.1093/mollus/eyab049">https://doi.org/10.1093/mollus/eyab049</a>.
  ieee: S. Perini, R. Butlin, A. M. Westram, and K. Johannesson, “Very short mountings
    are enough for sperm transfer in Littorina saxatilis,” <i>Journal of Molluscan
    Studies</i>, vol. 88, no. 1. Oxford Academic, 2022.
  ista: Perini S, Butlin R, Westram AM, Johannesson K. 2022. Very short mountings
    are enough for sperm transfer in Littorina saxatilis. Journal of Molluscan Studies.
    88(1), eyab049.
  mla: Perini, Samuel, et al. “Very Short Mountings Are Enough for Sperm Transfer
    in Littorina Saxatilis.” <i>Journal of Molluscan Studies</i>, vol. 88, no. 1,
    eyab049, Oxford Academic, 2022, doi:<a href="https://doi.org/10.1093/mollus/eyab049">10.1093/mollus/eyab049</a>.
  short: S. Perini, R. Butlin, A.M. Westram, K. Johannesson, Journal of Molluscan
    Studies 88 (2022).
date_created: 2022-03-27T22:01:46Z
date_published: 2022-03-01T00:00:00Z
date_updated: 2023-08-03T06:23:13Z
day: '01'
department:
- _id: BeVi
doi: 10.1093/mollus/eyab049
external_id:
  isi:
  - '000759081600002'
intvolume: '        88'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://eprints.whiterose.ac.uk/187332/
month: '03'
oa: 1
oa_version: Submitted Version
publication: Journal of Molluscan Studies
publication_identifier:
  eissn:
  - 1464-3766
  issn:
  - 0260-1230
publication_status: published
publisher: Oxford Academic
quality_controlled: '1'
scopus_import: '1'
status: public
title: Very short mountings are enough for sperm transfer in Littorina saxatilis
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 88
year: '2022'
...
---
_id: '10927'
abstract:
- lang: eng
  text: "Motivation\r\nHigh plasticity of bacterial genomes is provided by numerous
    mechanisms including horizontal gene transfer and recombination via numerous flanking
    repeats. Genome rearrangements such as inversions, deletions, insertions and duplications
    may independently occur in different strains, providing parallel adaptation or
    phenotypic diversity. Specifically, such rearrangements might be responsible for
    virulence, antibiotic resistance and antigenic variation. However, identification
    of such events requires laborious manual inspection and verification of phyletic
    pattern consistency.\r\nResults\r\nHere, we define the term ‘parallel rearrangements’
    as events that occur independently in phylogenetically distant bacterial strains
    and present a formalization of the problem of parallel rearrangements calling.
    We implement an algorithmic solution for the identification of parallel rearrangements
    in bacterial populations as a tool PaReBrick. The tool takes a collection of strains
    represented as a sequence of oriented synteny blocks and a phylogenetic tree as
    input data. It identifies rearrangements, tests them for consistency with a tree,
    and sorts the events by their parallelism score. The tool provides diagrams of
    the neighbors for each block of interest, allowing the detection of horizontally
    transferred blocks or their extra copies and the inversions in which copied blocks
    are involved. We demonstrated PaReBrick’s efficiency and accuracy and showed its
    potential to detect genome rearrangements responsible for pathogenicity and adaptation
    in bacterial genomes."
acknowledgement: "The authors thank the 2020 student class of the Bioinformatics Institute,
  who\r\nused the first versions of the tool and provided many valuable suggestions
  to\r\nimprove usability. They also thank Louisa Gonzalez Somermeyer for manuscript
  proofreading\r\nThis work was supported by the National Center for Cognitive Research
  of\r\nITMO University and JetBrains Research [to A.Z and N.A.]; and the European\r\nUnion’s
  Horizon 2020 Research and Innovation Programme under the Marie\r\nSkłodowska-Curie
  [754411 to O.B.].\r\nPaReBrick is written in Python and is available on GitHub:
  https://github.com/ctlab/parallel-rearrangements."
article_processing_charge: No
article_type: original
author:
- first_name: Alexey
  full_name: Zabelkin, Alexey
  last_name: Zabelkin
- first_name: Yulia
  full_name: Yakovleva, Yulia
  last_name: Yakovleva
- first_name: Olga
  full_name: Bochkareva, Olga
  id: C4558D3C-6102-11E9-A62E-F418E6697425
  last_name: Bochkareva
  orcid: 0000-0003-1006-6639
- first_name: Nikita
  full_name: Alexeev, Nikita
  last_name: Alexeev
citation:
  ama: 'Zabelkin A, Yakovleva Y, Bochkareva O, Alexeev N. PaReBrick: PArallel REarrangements
    and BReaks identification toolkit. <i>Bioinformatics</i>. 2022;38(2):357-363.
    doi:<a href="https://doi.org/10.1093/bioinformatics/btab691">10.1093/bioinformatics/btab691</a>'
  apa: 'Zabelkin, A., Yakovleva, Y., Bochkareva, O., &#38; Alexeev, N. (2022). PaReBrick:
    PArallel REarrangements and BReaks identification toolkit. <i>Bioinformatics</i>.
    Oxford Academic. <a href="https://doi.org/10.1093/bioinformatics/btab691">https://doi.org/10.1093/bioinformatics/btab691</a>'
  chicago: 'Zabelkin, Alexey, Yulia Yakovleva, Olga Bochkareva, and Nikita Alexeev.
    “PaReBrick: PArallel REarrangements and BReaks Identification Toolkit.” <i>Bioinformatics</i>.
    Oxford Academic, 2022. <a href="https://doi.org/10.1093/bioinformatics/btab691">https://doi.org/10.1093/bioinformatics/btab691</a>.'
  ieee: 'A. Zabelkin, Y. Yakovleva, O. Bochkareva, and N. Alexeev, “PaReBrick: PArallel
    REarrangements and BReaks identification toolkit,” <i>Bioinformatics</i>, vol.
    38, no. 2. Oxford Academic, pp. 357–363, 2022.'
  ista: 'Zabelkin A, Yakovleva Y, Bochkareva O, Alexeev N. 2022. PaReBrick: PArallel
    REarrangements and BReaks identification toolkit. Bioinformatics. 38(2), 357–363.'
  mla: 'Zabelkin, Alexey, et al. “PaReBrick: PArallel REarrangements and BReaks Identification
    Toolkit.” <i>Bioinformatics</i>, vol. 38, no. 2, Oxford Academic, 2022, pp. 357–63,
    doi:<a href="https://doi.org/10.1093/bioinformatics/btab691">10.1093/bioinformatics/btab691</a>.'
  short: A. Zabelkin, Y. Yakovleva, O. Bochkareva, N. Alexeev, Bioinformatics 38 (2022)
    357–363.
date_created: 2022-03-27T22:01:46Z
date_published: 2022-01-15T00:00:00Z
date_updated: 2023-08-03T06:21:46Z
day: '15'
ddc:
- '000'
department:
- _id: FyKo
doi: 10.1093/bioinformatics/btab691
ec_funded: 1
external_id:
  isi:
  - '000743380100008'
file:
- access_level: open_access
  checksum: 4b5688ff9ac86180ccdf7f82fa33d926
  content_type: application/pdf
  creator: dernst
  date_created: 2022-03-28T08:07:46Z
  date_updated: 2022-03-28T08:07:46Z
  file_id: '10930'
  file_name: 2022_Bioinformatics_Zabelkin.pdf
  file_size: 3425744
  relation: main_file
  success: 1
file_date_updated: 2022-03-28T08:07:46Z
has_accepted_license: '1'
intvolume: '        38'
isi: 1
issue: '2'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 357-363
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Bioinformatics
publication_identifier:
  eissn:
  - 1460-2059
  issn:
  - 1367-4803
publication_status: published
publisher: Oxford Academic
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://github.com/ctlab/parallel-rearrangements
scopus_import: '1'
status: public
title: 'PaReBrick: PArallel REarrangements and BReaks identification toolkit'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 38
year: '2022'
...
---
_id: '10934'
abstract:
- lang: eng
  text: 'FtsA is crucial for assembly of the E. coli divisome, as it dynamically links
    cytoplasmic FtsZ filaments with transmembrane cell division proteins. FtsA allegedly
    initiates cell division by switching from an inactive polymeric to an active monomeric
    confirmation, which recruits downstream proteins and stabilizes FtsZ filaments.
    Here, we use biochemical reconstitution experiments combined with quantitative
    fluorescence microscopy to study divisome activation in vitro. We compare wildtype-FtsA
    with FtsA-R286W, a constantly active gain-of-function mutant and find that R286W
    outperforms the wildtype protein in replicating FtsZ treadmilling dynamics, stabilizing
    FtsZ filaments and recruiting FtsN. We attribute these differences to a faster
    membrane exchange of FtsA-R286W and its higher packing density below FtsZ filaments.  Using
    FRET microscopy, we find that FtsN binding does not compete with, but promotes
    FtsA self-interaction. Our findings suggest a model where FtsA always forms dynamic
    polymers on the membrane, which re-organize during assembly and activation of
    the divisome. '
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
acknowledgement: We acknowledge members of the Loose laboratory at IST Austria for
  helpful discussions—in particular L. Lindorfer for his assistance with cloning and
  purifications. We thank J. Löwe and T. Nierhaus (MRC-LMB Cambridge, UK) for sharing
  unpublished work and helpful discussions, as well as D. Vavylonis and D. Rutkowski
  (Lehigh University, Bethlehem, PA, USA) as well as S. Martin (University of Lausanne,
  Switzerland) for sharing their code for FRAP analysis. We are also thankful for
  the support by the Scientific Service Units (SSU) of IST Austria through resources
  provided by the Imaging and Optics Facility (IOF) and the Lab Support Facility (LSF).
  This work was supported by the European Research Council through grant ERC 2015-StG-679239
  and by the Austrian Science Fund (FWF) StandAlone P34607 to M.L. and HFSP LT 000824/2016-L4
  to N.B. For the purpose of open access, we have applied a CC BY public copyright
  licence to any Author Accepted Manuscript version arising from this submission.
article_processing_charge: No
author:
- first_name: Philipp
  full_name: Radler, Philipp
  id: 40136C2A-F248-11E8-B48F-1D18A9856A87
  last_name: Radler
  orcid: ' 0000-0001-9198-2182 '
citation:
  ama: Radler P. In vitro reconstitution of Escherichia coli divisome activation.
    2022. doi:<a href="https://doi.org/10.15479/AT:ISTA:10934">10.15479/AT:ISTA:10934</a>
  apa: Radler, P. (2022). In vitro reconstitution of Escherichia coli divisome activation.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:10934">https://doi.org/10.15479/AT:ISTA:10934</a>
  chicago: Radler, Philipp. “In Vitro Reconstitution of Escherichia Coli Divisome
    Activation.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/AT:ISTA:10934">https://doi.org/10.15479/AT:ISTA:10934</a>.
  ieee: P. Radler, “In vitro reconstitution of Escherichia coli divisome activation.”
    Institute of Science and Technology Austria, 2022.
  ista: Radler P. 2022. In vitro reconstitution of Escherichia coli divisome activation,
    Institute of Science and Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:10934">10.15479/AT:ISTA:10934</a>.
  mla: Radler, Philipp. <i>In Vitro Reconstitution of Escherichia Coli Divisome Activation</i>.
    Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/AT:ISTA:10934">10.15479/AT:ISTA:10934</a>.
  short: P. Radler, (2022).
contributor:
- contributor_type: supervisor
  first_name: Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
- contributor_type: researcher
  first_name: Christoph M
  id: 4DF26D8C-F248-11E8-B48F-1D18A9856A87
  last_name: Sommer
- contributor_type: researcher
  first_name: Paulo
  last_name: Caldas
- contributor_type: researcher
  first_name: David
  id: B9577E20-AA38-11E9-AC9A-0930E6697425
  last_name: Michalik
- contributor_type: researcher
  first_name: Natalia
  last_name: Baranova
date_created: 2022-03-31T11:32:32Z
date_published: 2022-04-05T00:00:00Z
date_updated: 2024-02-21T12:35:18Z
day: '05'
ddc:
- '572'
department:
- _id: GradSch
- _id: MaLo
doi: 10.15479/AT:ISTA:10934
ec_funded: 1
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  date_created: 2022-04-22T10:15:19Z
  date_updated: 2022-04-22T10:15:19Z
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  date_updated: 2022-04-05T08:35:27Z
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  date_updated: 2022-04-05T08:37:02Z
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  date_created: 2022-04-05T15:06:08Z
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  creator: pradler
  date_created: 2022-04-22T09:42:56Z
  date_updated: 2022-04-22T09:42:56Z
  file_id: '11327'
  file_name: FRET_FtsN Effect.z08
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  success: 1
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  checksum: 640853788327aa2e30c0e1e5ce581eac
  content_type: application/octet-stream
  creator: pradler
  date_created: 2022-04-22T08:54:57Z
  date_updated: 2022-04-22T08:54:57Z
  file_id: '11318'
  file_name: FRET_FtsN Effect.z09
  file_size: 4294960000
  relation: main_file
  success: 1
- access_level: open_access
  checksum: 8797b4b42a8b5558029201f01eceffd0
  content_type: application/x-zip-compressed
  creator: pradler
  date_created: 2022-04-05T08:33:57Z
  date_updated: 2022-04-05T08:33:57Z
  file_id: '10950'
  file_name: Raw Microscopy_Dual Color FtsA His6 & FtsZ_FtsN effect.zip
  file_size: 2096740193
  relation: main_file
  success: 1
- access_level: open_access
  checksum: 3f1d75902b75e108ecff36522ddf252e
  content_type: application/x-zip-compressed
  creator: pradler
  date_created: 2022-04-05T08:50:43Z
  date_updated: 2022-04-05T08:50:43Z
  file_id: '10954'
  file_name: Raw Microscopy_FRET FtsA His6 + FtsN & FtsZ_01.zip
  file_size: 1259420774
  relation: main_file
  success: 1
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  checksum: 3f4928a36e1b1f295054668060df3079
  content_type: application/octet-stream
  creator: pradler
  date_created: 2022-04-05T08:51:55Z
  date_updated: 2022-04-05T08:51:55Z
  file_id: '10953'
  file_name: Raw Microscopy_FRET FtsA His6 + FtsN & FtsZ_01.z01
  file_size: 4294960000
  relation: main_file
  success: 1
file_date_updated: 2022-04-22T10:15:19Z
has_accepted_license: '1'
keyword:
- Bacterial cell division
- in vitro reconstitution
- FtsZ
- FtsN
- FtsA
month: '04'
oa: 1
oa_version: Submitted Version
project:
- _id: 2595697A-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '679239'
  name: Self-Organization of the Bacterial Cell
- _id: fc38323b-9c52-11eb-aca3-ff8afb4a011d
  grant_number: P34607
  name: "Understanding bacterial cell division by in vitro\r\nreconstitution"
publisher: Institute of Science and Technology Austria
related_material:
  link:
  - description: A custom written code (FRAPdiff) to quantify the Off binding rate
      and Diffusion coefficient of membrane bound proteins. Written by Christoph Sommer.
    relation: software
    url: https://doi.org/10.5281/zenodo.6400639
  record:
  - id: '11373'
    relation: used_in_publication
    status: public
  - id: '14280'
    relation: used_in_publication
    status: public
status: public
title: In vitro reconstitution of Escherichia coli divisome activation
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2022'
...
---
_id: '10939'
abstract:
- lang: eng
  text: Understanding and characterising biochemical processes inside single cells
    requires experimental platforms that allow one to perturb and observe the dynamics
    of such processes as well as computational methods to build and parameterise models
    from the collected data. Recent progress with experimental platforms and optogenetics
    has made it possible to expose each cell in an experiment to an individualised
    input and automatically record cellular responses over days with fine time resolution.
    However, methods to infer parameters of stochastic kinetic models from single-cell
    longitudinal data have generally been developed under the assumption that experimental
    data is sparse and that responses of cells to at most a few different input perturbations
    can be observed. Here, we investigate and compare different approaches for calculating
    parameter likelihoods of single-cell longitudinal data based on approximations
    of the chemical master equation (CME) with a particular focus on coupling the
    linear noise approximation (LNA) or moment closure methods to a Kalman filter.
    We show that, as long as cells are measured sufficiently frequently, coupling
    the LNA to a Kalman filter allows one to accurately approximate likelihoods and
    to infer model parameters from data even in cases where the LNA provides poor
    approximations of the CME. Furthermore, the computational cost of filtering-based
    iterative likelihood evaluation scales advantageously in the number of measurement
    times and different input perturbations and is thus ideally suited for data obtained
    from modern experimental platforms. To demonstrate the practical usefulness of
    these results, we perform an experiment in which single cells, equipped with an
    optogenetic gene expression system, are exposed to various different light-input
    sequences and measured at several hundred time points and use parameter inference
    based on iterative likelihood evaluation to parameterise a stochastic model of
    the system.
acknowledgement: We thank Virgile Andreani for useful discussions about the model
  and parameter inference. We thank Johan Paulsson and Jeffrey J Tabor for kind gifts
  of plasmids. R was supported by the ANR grant CyberCircuits (ANR-18-CE91-0002).
  The funders had no role in study design, data collection and analysis, decision
  to publish, or preparation of the manuscript.
article_number: e1009950
article_processing_charge: No
article_type: original
author:
- first_name: Anđela
  full_name: Davidović, Anđela
  last_name: Davidović
- first_name: Remy P
  full_name: Chait, Remy P
  id: 3464AE84-F248-11E8-B48F-1D18A9856A87
  last_name: Chait
  orcid: 0000-0003-0876-3187
- first_name: Gregory
  full_name: Batt, Gregory
  last_name: Batt
- first_name: Jakob
  full_name: Ruess, Jakob
  id: 4A245D00-F248-11E8-B48F-1D18A9856A87
  last_name: Ruess
  orcid: 0000-0003-1615-3282
citation:
  ama: Davidović A, Chait RP, Batt G, Ruess J. Parameter inference for stochastic
    biochemical models from perturbation experiments parallelised at the single cell
    level. <i>PLoS Computational Biology</i>. 2022;18(3). doi:<a href="https://doi.org/10.1371/journal.pcbi.1009950">10.1371/journal.pcbi.1009950</a>
  apa: Davidović, A., Chait, R. P., Batt, G., &#38; Ruess, J. (2022). Parameter inference
    for stochastic biochemical models from perturbation experiments parallelised at
    the single cell level. <i>PLoS Computational Biology</i>. Public Library of Science.
    <a href="https://doi.org/10.1371/journal.pcbi.1009950">https://doi.org/10.1371/journal.pcbi.1009950</a>
  chicago: Davidović, Anđela, Remy P Chait, Gregory Batt, and Jakob Ruess. “Parameter
    Inference for Stochastic Biochemical Models from Perturbation Experiments Parallelised
    at the Single Cell Level.” <i>PLoS Computational Biology</i>. Public Library of
    Science, 2022. <a href="https://doi.org/10.1371/journal.pcbi.1009950">https://doi.org/10.1371/journal.pcbi.1009950</a>.
  ieee: A. Davidović, R. P. Chait, G. Batt, and J. Ruess, “Parameter inference for
    stochastic biochemical models from perturbation experiments parallelised at the
    single cell level,” <i>PLoS Computational Biology</i>, vol. 18, no. 3. Public
    Library of Science, 2022.
  ista: Davidović A, Chait RP, Batt G, Ruess J. 2022. Parameter inference for stochastic
    biochemical models from perturbation experiments parallelised at the single cell
    level. PLoS Computational Biology. 18(3), e1009950.
  mla: Davidović, Anđela, et al. “Parameter Inference for Stochastic Biochemical Models
    from Perturbation Experiments Parallelised at the Single Cell Level.” <i>PLoS
    Computational Biology</i>, vol. 18, no. 3, e1009950, Public Library of Science,
    2022, doi:<a href="https://doi.org/10.1371/journal.pcbi.1009950">10.1371/journal.pcbi.1009950</a>.
  short: A. Davidović, R.P. Chait, G. Batt, J. Ruess, PLoS Computational Biology 18
    (2022).
date_created: 2022-04-03T22:01:42Z
date_published: 2022-03-18T00:00:00Z
date_updated: 2022-04-04T10:21:53Z
day: '18'
ddc:
- '570'
- '000'
department:
- _id: CaGu
doi: 10.1371/journal.pcbi.1009950
file:
- access_level: open_access
  checksum: 458ef542761fb714ced214f240daf6b2
  content_type: application/pdf
  creator: dernst
  date_created: 2022-04-04T10:14:39Z
  date_updated: 2022-04-04T10:14:39Z
  file_id: '10947'
  file_name: 2022_PLoSCompBio_Davidovic.pdf
  file_size: 2958642
  relation: main_file
  success: 1
file_date_updated: 2022-04-04T10:14:39Z
has_accepted_license: '1'
intvolume: '        18'
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
publication: PLoS Computational Biology
publication_identifier:
  eissn:
  - 1553-7358
  issn:
  - 1553-734X
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://gitlab.pasteur.fr/adavidov/inferencelnakf
scopus_import: '1'
status: public
title: Parameter inference for stochastic biochemical models from perturbation experiments
  parallelised at the single cell level
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 18
year: '2022'
...
---
_id: '10940'
abstract:
- lang: eng
  text: 'Magnetic-field-resilient superconducting circuits enable sensing applications
    and hybrid quantum computing architectures involving spin or topological qubits
    and electromechanical elements, as well as studying flux noise and quasiparticle
    loss. We investigate the effect of in-plane magnetic fields up to 1 T on the spectrum
    and coherence times of thin-film three-dimensional aluminum transmons. Using a
    copper cavity, unaffected by strong magnetic fields, we can probe solely the effect
    of magnetic fields on the transmons. We present data on a single-junction and
    a superconducting-quantum-interference-device (SQUID) transmon that are cooled
    down in the same cavity. As expected, the transmon frequencies decrease with increasing
    field, due to suppression of the superconducting gap and a geometric Fraunhofer-like
    contribution. Nevertheless, the thin-film transmons show strong magnetic field
    resilience: both transmons display microsecond coherence up to at least 0.65 T,
    and T1 remains above 1μs over the entire measurable range. SQUID spectroscopy
    is feasible up to 1 T, the limit of our magnet. We conclude that thin-film aluminum
    Josephson junctions are suitable hardware for superconducting circuits in the
    high-magnetic-field regime.'
acknowledgement: "We would like to thank Ida Milow for her internship in the laboratory
  and contributions to our code base. We thank T. Zent and L. Hamdan for technical
  assistance, and D. Fan for help with setting up the aluminum evaporator. We thank
  A. Salari, M. Rößler, S. Barzanjeh, M. Zemlicka, F. Hassani, and M. Peruzzo for
  contributions in the early stages of the experiments. This project has received
  funding from the European Research Council (ERC) under the European Union’s Horizon
  2020 research and innovation program (Grant Agreement No. 741121) and was also funded
  by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under CRC
  1238 – 277146847 (Subproject B01), as well as under Germany’s Excellence Strategy
  – Cluster of Excellence Matter and Light for Quantum Computing (ML4Q), EXC 2004/1\r\n–
  390534769."
article_number: '034032'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: J.
  full_name: Krause, J.
  last_name: Krause
- first_name: C.
  full_name: Dickel, C.
  last_name: Dickel
- first_name: E.
  full_name: Vaal, E.
  last_name: Vaal
- first_name: M.
  full_name: Vielmetter, M.
  last_name: Vielmetter
- first_name: J.
  full_name: Feng, J.
  last_name: Feng
- first_name: R.
  full_name: Bounds, R.
  last_name: Bounds
- first_name: G.
  full_name: Catelani, G.
  last_name: Catelani
- first_name: Johannes M
  full_name: Fink, Johannes M
  id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
  last_name: Fink
  orcid: 0000-0001-8112-028X
- first_name: Yoichi
  full_name: Ando, Yoichi
  last_name: Ando
citation:
  ama: Krause J, Dickel C, Vaal E, et al. Magnetic field resilience of three-dimensional
    transmons with thin-film Al/AlOx/Al Josephson junctions approaching 1 T. <i>Physical
    Review Applied</i>. 2022;17(3). doi:<a href="https://doi.org/10.1103/PhysRevApplied.17.034032">10.1103/PhysRevApplied.17.034032</a>
  apa: Krause, J., Dickel, C., Vaal, E., Vielmetter, M., Feng, J., Bounds, R., … Ando,
    Y. (2022). Magnetic field resilience of three-dimensional transmons with thin-film
    Al/AlOx/Al Josephson junctions approaching 1 T. <i>Physical Review Applied</i>.
    American Physical Society. <a href="https://doi.org/10.1103/PhysRevApplied.17.034032">https://doi.org/10.1103/PhysRevApplied.17.034032</a>
  chicago: Krause, J., C. Dickel, E. Vaal, M. Vielmetter, J. Feng, R. Bounds, G. Catelani,
    Johannes M Fink, and Yoichi Ando. “Magnetic Field Resilience of Three-Dimensional
    Transmons with Thin-Film Al/AlOx/Al Josephson Junctions Approaching 1 T.” <i>Physical
    Review Applied</i>. American Physical Society, 2022. <a href="https://doi.org/10.1103/PhysRevApplied.17.034032">https://doi.org/10.1103/PhysRevApplied.17.034032</a>.
  ieee: J. Krause <i>et al.</i>, “Magnetic field resilience of three-dimensional transmons
    with thin-film Al/AlOx/Al Josephson junctions approaching 1 T,” <i>Physical Review
    Applied</i>, vol. 17, no. 3. American Physical Society, 2022.
  ista: Krause J, Dickel C, Vaal E, Vielmetter M, Feng J, Bounds R, Catelani G, Fink
    JM, Ando Y. 2022. Magnetic field resilience of three-dimensional transmons with
    thin-film Al/AlOx/Al Josephson junctions approaching 1 T. Physical Review Applied.
    17(3), 034032.
  mla: Krause, J., et al. “Magnetic Field Resilience of Three-Dimensional Transmons
    with Thin-Film Al/AlOx/Al Josephson Junctions Approaching 1 T.” <i>Physical Review
    Applied</i>, vol. 17, no. 3, 034032, American Physical Society, 2022, doi:<a href="https://doi.org/10.1103/PhysRevApplied.17.034032">10.1103/PhysRevApplied.17.034032</a>.
  short: J. Krause, C. Dickel, E. Vaal, M. Vielmetter, J. Feng, R. Bounds, G. Catelani,
    J.M. Fink, Y. Ando, Physical Review Applied 17 (2022).
date_created: 2022-04-03T22:01:43Z
date_published: 2022-03-11T00:00:00Z
date_updated: 2023-08-03T06:23:58Z
day: '11'
department:
- _id: JoFi
doi: 10.1103/PhysRevApplied.17.034032
external_id:
  arxiv:
  - '2111.01115'
  isi:
  - '000770371400003'
intvolume: '        17'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2111.01115
month: '03'
oa: 1
oa_version: Preprint
publication: Physical Review Applied
publication_identifier:
  eissn:
  - 2331-7019
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Magnetic field resilience of three-dimensional transmons with thin-film Al/AlOx/Al
  Josephson junctions approaching 1 T
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 17
year: '2022'
...
---
_id: '10945'
abstract:
- lang: eng
  text: Mica-titania pearlescent pigments (MTs) were previously coated with organic
    molecules to obtain combination pigments (CPs) for achieving certain improvements
    or functionalities. Anthocyanins (ACNs) are molecules that can be extracted from
    natural resources and exhibit color changes via pH modifications of the enclosing
    medium. The purpose of the study was to produce a new series of CPs by depositing
    ACNs on MTs at different pH values, to observe the changes in color, and to associate
    these changes to thermogravimetrically determined deposition efficiencies in light
    of spectral differences. The extraction and deposition methods were based on aqueous
    chemistry and were straightforward. The ACN deposition generally increased with
    increasing pH and correlated with the consistency between the charges of the MT
    surfaces and the dominant ACN species at a specific pH value. The fluorescence
    of the CPs was inversely correlated with the deposition quantities invoking the
    possibility of a quenching effect.
acknowledgement: "This research was partly funded by Hacettepe University (Bilimsel
  Ara¸stırma Projeleri\r\nKoordinasyon Birimi), grant number FHD-2015-8094.The authors
  are indebted to Ahmet Önal for his supports in acquiring the fluorescence spectra
  and the decision of excitation wavelengths. The authors also acknowledge use of
  the services and facilities of UNAM-National Nanotechnology Research Center at Bilkent
  University and mica donation from Sabuncular Mining Co."
article_processing_charge: Yes
article_type: original
author:
- first_name: Mehmet Orkun
  full_name: Çoruh, Mehmet Orkun
  id: d25163e5-8d53-11eb-a251-e6dd8ea1b8ef
  last_name: Çoruh
  orcid: 0000-0002-3219-2022
- first_name: Güngör
  full_name: Gündüz, Güngör
  last_name: Gündüz
- first_name: Üner
  full_name: Çolak, Üner
  last_name: Çolak
- first_name: Bora
  full_name: Maviş, Bora
  last_name: Maviş
citation:
  ama: Çoruh MO, Gündüz G, Çolak Ü, Maviş B. pH-dependent coloring of combination
    effect pigments with anthocyanins from Brassica oleracea var. capitata F. rubra.
    <i>Colorants</i>. 2022;1(2):149-164. doi:<a href="https://doi.org/10.3390/colorants1020010">10.3390/colorants1020010</a>
  apa: Çoruh, M. O., Gündüz, G., Çolak, Ü., &#38; Maviş, B. (2022). pH-dependent coloring
    of combination effect pigments with anthocyanins from Brassica oleracea var. capitata
    F. rubra. <i>Colorants</i>. MDPI. <a href="https://doi.org/10.3390/colorants1020010">https://doi.org/10.3390/colorants1020010</a>
  chicago: Çoruh, Mehmet Orkun, Güngör Gündüz, Üner Çolak, and Bora Maviş. “PH-Dependent
    Coloring of Combination Effect Pigments with Anthocyanins from Brassica Oleracea
    Var. Capitata F. Rubra.” <i>Colorants</i>. MDPI, 2022. <a href="https://doi.org/10.3390/colorants1020010">https://doi.org/10.3390/colorants1020010</a>.
  ieee: M. O. Çoruh, G. Gündüz, Ü. Çolak, and B. Maviş, “pH-dependent coloring of
    combination effect pigments with anthocyanins from Brassica oleracea var. capitata
    F. rubra,” <i>Colorants</i>, vol. 1, no. 2. MDPI, pp. 149–164, 2022.
  ista: Çoruh MO, Gündüz G, Çolak Ü, Maviş B. 2022. pH-dependent coloring of combination
    effect pigments with anthocyanins from Brassica oleracea var. capitata F. rubra.
    Colorants. 1(2), 149–164.
  mla: Çoruh, Mehmet Orkun, et al. “PH-Dependent Coloring of Combination Effect Pigments
    with Anthocyanins from Brassica Oleracea Var. Capitata F. Rubra.” <i>Colorants</i>,
    vol. 1, no. 2, MDPI, 2022, pp. 149–64, doi:<a href="https://doi.org/10.3390/colorants1020010">10.3390/colorants1020010</a>.
  short: M.O. Çoruh, G. Gündüz, Ü. Çolak, B. Maviş, Colorants 1 (2022) 149–164.
date_created: 2022-04-04T09:03:54Z
date_published: 2022-04-01T00:00:00Z
date_updated: 2023-08-09T10:12:22Z
day: '01'
ddc:
- '570'
department:
- _id: LeSa
doi: 10.3390/colorants1020010
file:
- access_level: open_access
  checksum: 2c15c8d3041ebc36bc64870247081758
  content_type: application/pdf
  creator: dernst
  date_created: 2022-04-04T10:39:24Z
  date_updated: 2022-04-04T10:39:24Z
  file_id: '10949'
  file_name: 2022_Colorants_Coruh.pdf
  file_size: 2437988
  relation: main_file
  success: 1
file_date_updated: 2022-04-04T10:39:24Z
has_accepted_license: '1'
intvolume: '         1'
issue: '2'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 149-164
publication: Colorants
publication_identifier:
  issn:
  - 2079-6447
publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: pH-dependent coloring of combination effect pigments with anthocyanins from
  Brassica oleracea var. capitata F. rubra
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 1
year: '2022'
...
---
_id: '11128'
abstract:
- lang: eng
  text: "Although we often see studies focusing on simple or even discrete traits
    in studies of colouration,\r\nthe variation of “appearance” phenotypes found in
    nature is often more complex, continuous\r\nand high-dimensional. Therefore, we
    developed automated methods suitable for large datasets\r\nof genomes and images,
    striving to account for their complex nature, while minimising human\r\nbias.
    We used these methods on a dataset of more than 20, 000 plant SNP genomes and\r\ncorresponding
    fower images from a hybrid zone of two subspecies of Antirrhinum majus with\r\ndistinctly
    coloured fowers to improve our understanding of the genetic nature of the fower\r\ncolour
    in our study system.\r\nFirstly, we use the advantage of large numbers of genotyped
    plants to estimate the haplotypes in\r\nthe main fower colour regulating region.
    We study colour- and geography-related characteristics\r\nof the estimated haplotypes
    and how they connect to their relatedness. We show discrepancies\r\nfrom the expected
    fower colour distributions given the genotype and identify particular\r\nhaplotypes
    leading to unexpected phenotypes. We also confrm a signifcant defcit of the\r\ndouble
    recessive recombinant and quite surprisingly, we show that haplotypes of the most\r\nfrequent
    parental type are much less variable than others.\r\nSecondly, we introduce our
    pipeline capable of processing tens of thousands of full fower\r\nimages without
    human interaction and summarising each image into a set of informative scores.\r\nWe
    show the compatibility of these machine-measured fower colour scores with the
    previously\r\nused manual scores and study impact of external efect on the resulting
    scores. Finally, we use\r\nthe machine-measured fower colour scores to ft and
    examine a phenotype cline across the\r\nhybrid zone in Planoles using full fower
    images as opposed to discrete, manual scores and\r\ncompare it with the genotypic
    cline."
acknowledged_ssus:
- _id: ScienComp
- _id: Bio
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Lenka
  full_name: Matejovicova, Lenka
  id: 2DFDEC72-F248-11E8-B48F-1D18A9856A87
  last_name: Matejovicova
citation:
  ama: Matejovicova L. Genetic basis of flower colour as a model for adaptive evolution.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:11128">10.15479/at:ista:11128</a>
  apa: Matejovicova, L. (2022). <i>Genetic basis of flower colour as a model for adaptive
    evolution</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11128">https://doi.org/10.15479/at:ista:11128</a>
  chicago: Matejovicova, Lenka. “Genetic Basis of Flower Colour as a Model for Adaptive
    Evolution.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11128">https://doi.org/10.15479/at:ista:11128</a>.
  ieee: L. Matejovicova, “Genetic basis of flower colour as a model for adaptive evolution,”
    Institute of Science and Technology Austria, 2022.
  ista: Matejovicova L. 2022. Genetic basis of flower colour as a model for adaptive
    evolution. Institute of Science and Technology Austria.
  mla: Matejovicova, Lenka. <i>Genetic Basis of Flower Colour as a Model for Adaptive
    Evolution</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11128">10.15479/at:ista:11128</a>.
  short: L. Matejovicova, Genetic Basis of Flower Colour as a Model for Adaptive Evolution,
    Institute of Science and Technology Austria, 2022.
date_created: 2022-04-07T08:19:54Z
date_published: 2022-04-06T00:00:00Z
date_updated: 2023-06-23T06:26:41Z
day: '06'
ddc:
- '576'
- '582'
degree_awarded: PhD
department:
- _id: GradSch
- _id: NiBa
doi: 10.15479/at:ista:11128
file:
- access_level: open_access
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  file_name: LenkaPhD Official_source.zip
  file_size: 23036766
  relation: source_file
file_date_updated: 2022-04-07T08:11:51Z
has_accepted_license: '1'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: '112'
publication_identifier:
  isbn:
  - 978-3-99078-016-9
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
title: Genetic basis of flower colour as a model for adaptive evolution
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2022'
...
---
_id: '11135'
abstract:
- lang: eng
  text: We consider a correlated NxN Hermitian random matrix with a polynomially decaying
    metric correlation structure. By calculating the trace of the moments of the matrix
    and using the summable decay of the cumulants, we show that its operator norm
    is stochastically dominated by one.
article_number: '2250036'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Jana
  full_name: Reker, Jana
  id: e796e4f9-dc8d-11ea-abe3-97e26a0323e9
  last_name: Reker
citation:
  ama: 'Reker J. On the operator norm of a Hermitian random matrix with correlated
    entries. <i>Random Matrices: Theory and Applications</i>. 2022;11(4). doi:<a href="https://doi.org/10.1142/s2010326322500368">10.1142/s2010326322500368</a>'
  apa: 'Reker, J. (2022). On the operator norm of a Hermitian random matrix with correlated
    entries. <i>Random Matrices: Theory and Applications</i>. World Scientific. <a
    href="https://doi.org/10.1142/s2010326322500368">https://doi.org/10.1142/s2010326322500368</a>'
  chicago: 'Reker, Jana. “On the Operator Norm of a Hermitian Random Matrix with Correlated
    Entries.” <i>Random Matrices: Theory and Applications</i>. World Scientific, 2022.
    <a href="https://doi.org/10.1142/s2010326322500368">https://doi.org/10.1142/s2010326322500368</a>.'
  ieee: 'J. Reker, “On the operator norm of a Hermitian random matrix with correlated
    entries,” <i>Random Matrices: Theory and Applications</i>, vol. 11, no. 4. World
    Scientific, 2022.'
  ista: 'Reker J. 2022. On the operator norm of a Hermitian random matrix with correlated
    entries. Random Matrices: Theory and Applications. 11(4), 2250036.'
  mla: 'Reker, Jana. “On the Operator Norm of a Hermitian Random Matrix with Correlated
    Entries.” <i>Random Matrices: Theory and Applications</i>, vol. 11, no. 4, 2250036,
    World Scientific, 2022, doi:<a href="https://doi.org/10.1142/s2010326322500368">10.1142/s2010326322500368</a>.'
  short: 'J. Reker, Random Matrices: Theory and Applications 11 (2022).'
date_created: 2022-04-08T07:11:12Z
date_published: 2022-10-01T00:00:00Z
date_updated: 2023-08-03T06:32:22Z
day: '01'
department:
- _id: GradSch
- _id: LaEr
doi: 10.1142/s2010326322500368
external_id:
  arxiv:
  - '2103.03906'
  isi:
  - '000848873800001'
intvolume: '        11'
isi: 1
issue: '4'
keyword:
- Discrete Mathematics and Combinatorics
- Statistics
- Probability and Uncertainty
- Statistics and Probability
- Algebra and Number Theory
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: ' https://doi.org/10.48550/arXiv.2103.03906'
month: '10'
oa: 1
oa_version: Preprint
publication: 'Random Matrices: Theory and Applications'
publication_identifier:
  eissn:
  - 2010-3271
  issn:
  - 2010-3263
publication_status: published
publisher: World Scientific
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the operator norm of a Hermitian random matrix with correlated entries
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 11
year: '2022'
...
---
_id: '11142'
abstract:
- lang: eng
  text: SnTe is a promising Pb-free thermoelectric (TE) material with high electrical
    conductivity. We discovered the synergistic effect of Bi2O3 on enhancing the average
    power factor (PF) and overall ZT value of the SnTe-based thermoelectric material.
    The introduction of Bi2O3 forms plenty of SnO2, Bi2O3, and Bi-rich nanoprecipitates.
    These interfaces between the SnTe matrix and the nanoprecipitates can enhance
    the average PF through the energy filtering effect. On the other hand, abundant
    and diverse nanoprecipitates can significantly diminish the lattice thermal conductivity
    (κlat) through enhanced phonon scattering. The synergistic effect of Bi2O3 resulted
    in a maximum ZT (ZTmax) value of 0.9 at SnTe-2% Bi2O3 and an average ZT (ZTave)
    value of 0.4 for SnTe-4% Bi2O3 from 300 K to 823 K. The work provides an excellent
    reference to develop non-toxic high-performance TE materials.
acknowledgement: This work was supported by National Natural Science Foundation of
  China (52002042), National Key Research and Development Program of China (2018YFA0702100
  and 2018YFB0703600), 111 Project (B17002) and Lise Meitner Project M 2889-N. This
  work was also supported by the National Postdoctoral Program for Innovative Talents
  (BX20200028). L.D.Z. appreciates the support of the high-performance computing (HPC)
  resources at Beihang University, the National Science Fund for Distinguished Young
  Scholars (51925101), and center for High Pressure Science and Technology Advanced
  Research (HPSTAR) for SEM and TEM measurements.
article_number: '100985'
article_processing_charge: No
article_type: original
author:
- first_name: Tao
  full_name: Hong, Tao
  last_name: Hong
- first_name: Changrong
  full_name: Guo, Changrong
  last_name: Guo
- first_name: Dongyang
  full_name: Wang, Dongyang
  last_name: Wang
- first_name: Bingchao
  full_name: Qin, Bingchao
  last_name: Qin
- first_name: Cheng
  full_name: Chang, Cheng
  id: 9E331C2E-9F27-11E9-AE48-5033E6697425
  last_name: Chang
  orcid: 0000-0002-9515-4277
- first_name: Xiang
  full_name: Gao, Xiang
  last_name: Gao
- first_name: Li Dong
  full_name: Zhao, Li Dong
  last_name: Zhao
citation:
  ama: Hong T, Guo C, Wang D, et al. Enhanced thermoelectric performance in SnTe due
    to the energy filtering effect introduced by Bi2O3. <i>Materials Today Energy</i>.
    2022;25. doi:<a href="https://doi.org/10.1016/j.mtener.2022.100985">10.1016/j.mtener.2022.100985</a>
  apa: Hong, T., Guo, C., Wang, D., Qin, B., Chang, C., Gao, X., &#38; Zhao, L. D.
    (2022). Enhanced thermoelectric performance in SnTe due to the energy filtering
    effect introduced by Bi2O3. <i>Materials Today Energy</i>. Elsevier. <a href="https://doi.org/10.1016/j.mtener.2022.100985">https://doi.org/10.1016/j.mtener.2022.100985</a>
  chicago: Hong, Tao, Changrong Guo, Dongyang Wang, Bingchao Qin, Cheng Chang, Xiang
    Gao, and Li Dong Zhao. “Enhanced Thermoelectric Performance in SnTe Due to the
    Energy Filtering Effect Introduced by Bi2O3.” <i>Materials Today Energy</i>. Elsevier,
    2022. <a href="https://doi.org/10.1016/j.mtener.2022.100985">https://doi.org/10.1016/j.mtener.2022.100985</a>.
  ieee: T. Hong <i>et al.</i>, “Enhanced thermoelectric performance in SnTe due to
    the energy filtering effect introduced by Bi2O3,” <i>Materials Today Energy</i>,
    vol. 25. Elsevier, 2022.
  ista: Hong T, Guo C, Wang D, Qin B, Chang C, Gao X, Zhao LD. 2022. Enhanced thermoelectric
    performance in SnTe due to the energy filtering effect introduced by Bi2O3. Materials
    Today Energy. 25, 100985.
  mla: Hong, Tao, et al. “Enhanced Thermoelectric Performance in SnTe Due to the Energy
    Filtering Effect Introduced by Bi2O3.” <i>Materials Today Energy</i>, vol. 25,
    100985, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.mtener.2022.100985">10.1016/j.mtener.2022.100985</a>.
  short: T. Hong, C. Guo, D. Wang, B. Qin, C. Chang, X. Gao, L.D. Zhao, Materials
    Today Energy 25 (2022).
date_created: 2022-04-10T22:01:39Z
date_published: 2022-04-01T00:00:00Z
date_updated: 2023-08-03T06:28:16Z
day: '01'
department:
- _id: MaIb
doi: 10.1016/j.mtener.2022.100985
external_id:
  isi:
  - '000798679100010'
intvolume: '        25'
isi: 1
language:
- iso: eng
month: '04'
oa_version: None
project:
- _id: 9B8804FC-BA93-11EA-9121-9846C619BF3A
  grant_number: M02889
  name: Bottom-up Engineering for Thermoelectric Applications
publication: Materials Today Energy
publication_identifier:
  eissn:
  - 2468-6069
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Enhanced thermoelectric performance in SnTe due to the energy filtering effect
  introduced by Bi2O3
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 25
year: '2022'
...
---
_id: '11143'
abstract:
- lang: eng
  text: 'Dravet syndrome is a neurodevelopmental disorder characterized by epilepsy,
    intellectual disability, and sudden death due to pathogenic variants in SCN1A
    with loss of function of the sodium channel subunit Nav1.1. Nav1.1-expressing
    parvalbumin GABAergic interneurons (PV-INs) from young Scn1a+/− mice show impaired
    action potential generation. An approach assessing PV-IN function in the same
    mice at two time points shows impaired spike generation in all Scn1a+/− mice at
    postnatal days (P) 16–21, whether deceased prior or surviving to P35, with normalization
    by P35 in surviving mice. However, PV-IN synaptic transmission is dysfunctional
    in young Scn1a+/− mice that did not survive and in Scn1a+/− mice ≥ P35. Modeling
    confirms that PV-IN axonal propagation is more sensitive to decreased sodium conductance
    than spike generation. These results demonstrate dynamic dysfunction in Dravet
    syndrome: combined abnormalities of PV-IN spike generation and propagation drives
    early disease severity, while ongoing dysfunction of synaptic transmission contributes
    to chronic pathology.'
acknowledgement: We would like to thank Bernardo Rudy, Joanna Mattis, and Laura Mcgarry
  for comments on a previous version of the manuscript; Xiaohong Zhang for expert
  technical support and mouse colony maintenance; Melody Cheng for assistance with
  generation of the graphical abstract; and Jennifer Kearney for the gift of Scn1a+/−
  mice. This work was supported by the National Institute of Neurological Disorders
  and Stroke of the National Institutes of Health under F31NS111803 (to K.M.G.) and
  K08NS097633 and R01NS110869 (to E.M.G.), the Dravet Syndrome Foundation (to A.S.),
  an ERC Consolidator Grant (SYNAPSEEK) (to T.P.V.), and the NOMIS Foundation through
  the NOMIS Fellowships program at IST Austria (to C.C.). The graphical abstract was
  prepared using BioRender software (BioRender.com).
article_number: '110580'
article_processing_charge: No
article_type: original
author:
- first_name: Keisuke
  full_name: Kaneko, Keisuke
  last_name: Kaneko
- first_name: Christopher
  full_name: Currin, Christopher
  id: e8321fc5-3091-11eb-8a53-83f309a11ac9
  last_name: Currin
  orcid: 0000-0002-4809-5059
- first_name: Kevin M.
  full_name: Goff, Kevin M.
  last_name: Goff
- first_name: Eric R.
  full_name: Wengert, Eric R.
  last_name: Wengert
- first_name: Ala
  full_name: Somarowthu, Ala
  last_name: Somarowthu
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
- first_name: Ethan M.
  full_name: Goldberg, Ethan M.
  last_name: Goldberg
citation:
  ama: Kaneko K, Currin C, Goff KM, et al. Developmentally regulated impairment of
    parvalbumin interneuron synaptic transmission in an experimental model of Dravet
    syndrome. <i>Cell Reports</i>. 2022;38(13). doi:<a href="https://doi.org/10.1016/j.celrep.2022.110580">10.1016/j.celrep.2022.110580</a>
  apa: Kaneko, K., Currin, C., Goff, K. M., Wengert, E. R., Somarowthu, A., Vogels,
    T. P., &#38; Goldberg, E. M. (2022). Developmentally regulated impairment of parvalbumin
    interneuron synaptic transmission in an experimental model of Dravet syndrome.
    <i>Cell Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2022.110580">https://doi.org/10.1016/j.celrep.2022.110580</a>
  chicago: Kaneko, Keisuke, Christopher Currin, Kevin M. Goff, Eric R. Wengert, Ala
    Somarowthu, Tim P Vogels, and Ethan M. Goldberg. “Developmentally Regulated Impairment
    of Parvalbumin Interneuron Synaptic Transmission in an Experimental Model of Dravet
    Syndrome.” <i>Cell Reports</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.celrep.2022.110580">https://doi.org/10.1016/j.celrep.2022.110580</a>.
  ieee: K. Kaneko <i>et al.</i>, “Developmentally regulated impairment of parvalbumin
    interneuron synaptic transmission in an experimental model of Dravet syndrome,”
    <i>Cell Reports</i>, vol. 38, no. 13. Elsevier, 2022.
  ista: Kaneko K, Currin C, Goff KM, Wengert ER, Somarowthu A, Vogels TP, Goldberg
    EM. 2022. Developmentally regulated impairment of parvalbumin interneuron synaptic
    transmission in an experimental model of Dravet syndrome. Cell Reports. 38(13),
    110580.
  mla: Kaneko, Keisuke, et al. “Developmentally Regulated Impairment of Parvalbumin
    Interneuron Synaptic Transmission in an Experimental Model of Dravet Syndrome.”
    <i>Cell Reports</i>, vol. 38, no. 13, 110580, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.celrep.2022.110580">10.1016/j.celrep.2022.110580</a>.
  short: K. Kaneko, C. Currin, K.M. Goff, E.R. Wengert, A. Somarowthu, T.P. Vogels,
    E.M. Goldberg, Cell Reports 38 (2022).
date_created: 2022-04-10T22:01:39Z
date_published: 2022-03-29T00:00:00Z
date_updated: 2023-08-03T06:32:55Z
day: '29'
ddc:
- '570'
department:
- _id: TiVo
doi: 10.1016/j.celrep.2022.110580
ec_funded: 1
external_id:
  isi:
  - '000779794000001'
file:
- access_level: open_access
  checksum: 49105c6c27c9af0f37f50a8bbb4d380d
  content_type: application/pdf
  creator: dernst
  date_created: 2022-04-15T11:00:58Z
  date_updated: 2022-04-15T11:00:58Z
  file_id: '11172'
  file_name: 2022_CellReports_Kaneko.pdf
  file_size: 4774216
  relation: main_file
  success: 1
file_date_updated: 2022-04-15T11:00:58Z
has_accepted_license: '1'
intvolume: '        38'
isi: 1
issue: '13'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
project:
- _id: 0aacfa84-070f-11eb-9043-d7eb2c709234
  call_identifier: H2020
  grant_number: '819603'
  name: Learning the shape of synaptic plasticity rules for neuronal architectures
    and function through machine learning.
- _id: 9B861AAC-BA93-11EA-9121-9846C619BF3A
  name: NOMIS Fellowship Program
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Developmentally regulated impairment of parvalbumin interneuron synaptic transmission
  in an experimental model of Dravet syndrome
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 38
year: '2022'
...
---
_id: '11144'
abstract:
- lang: eng
  text: Thermoelectric materials allow for direct conversion between heat and electricity,
    offering the potential for power generation. The average dimensionless figure
    of merit ZTave determines device efficiency. N-type tin selenide crystals exhibit
    outstanding three-dimensional charge and two-dimensional phonon transport along
    the out-of-plane direction, contributing to a high maximum figure of merit Zmax
    of ~3.6 × 10−3 per kelvin but a moderate ZTave of ~1.1. We found an attractive
    high Zmax of ~4.1 × 10−3 per kelvin at 748 kelvin and a ZTave of ~1.7 at 300 to
    773 kelvin in chlorine-doped and lead-alloyed tin selenide crystals by phonon-electron
    decoupling. The chlorine-induced low deformation potential improved the carrier
    mobility. The lead-induced mass and strain fluctuations reduced the lattice thermal
    conductivity. Phonon-electron decoupling plays a critical role to achieve high-performance
    thermoelectrics.
acknowledgement: This work was supported by the Basic Science Center Project of the
  National Natural Science Foundation of China (51788104), the National Key Research
  and Development Program of China (2018YFA0702100), the National Science Fund for
  Distinguished Young Scholars (51925101), the 111 Project (B17002), the Lise Meitner
  Project (M2889-N), and the National Key Research and Development Program of China
  (2018YFB0703600). This work is also supported by the National Postdoctoral Program
  for Innovative Talents (BX20200028). L.-D.Z. is thankful for the high-performance
  computing resources at Beihang University.
article_processing_charge: No
article_type: original
author:
- first_name: Lizhong
  full_name: Su, Lizhong
  last_name: Su
- first_name: Dongyang
  full_name: Wang, Dongyang
  last_name: Wang
- first_name: Sining
  full_name: Wang, Sining
  last_name: Wang
- first_name: Bingchao
  full_name: Qin, Bingchao
  last_name: Qin
- first_name: Yuping
  full_name: Wang, Yuping
  last_name: Wang
- first_name: Yongxin
  full_name: Qin, Yongxin
  last_name: Qin
- first_name: Yang
  full_name: Jin, Yang
  last_name: Jin
- first_name: Cheng
  full_name: Chang, Cheng
  id: 9E331C2E-9F27-11E9-AE48-5033E6697425
  last_name: Chang
  orcid: 0000-0002-9515-4277
- first_name: Li Dong
  full_name: Zhao, Li Dong
  last_name: Zhao
citation:
  ama: Su L, Wang D, Wang S, et al. High thermoelectric performance realized through
    manipulating layered phonon-electron decoupling. <i>Science</i>. 2022;375(6587):1385-1389.
    doi:<a href="https://doi.org/10.1126/science.abn8997">10.1126/science.abn8997</a>
  apa: Su, L., Wang, D., Wang, S., Qin, B., Wang, Y., Qin, Y., … Zhao, L. D. (2022).
    High thermoelectric performance realized through manipulating layered phonon-electron
    decoupling. <i>Science</i>. American Association for the Advancement of Science.
    <a href="https://doi.org/10.1126/science.abn8997">https://doi.org/10.1126/science.abn8997</a>
  chicago: Su, Lizhong, Dongyang Wang, Sining Wang, Bingchao Qin, Yuping Wang, Yongxin
    Qin, Yang Jin, Cheng Chang, and Li Dong Zhao. “High Thermoelectric Performance
    Realized through Manipulating Layered Phonon-Electron Decoupling.” <i>Science</i>.
    American Association for the Advancement of Science, 2022. <a href="https://doi.org/10.1126/science.abn8997">https://doi.org/10.1126/science.abn8997</a>.
  ieee: L. Su <i>et al.</i>, “High thermoelectric performance realized through manipulating
    layered phonon-electron decoupling,” <i>Science</i>, vol. 375, no. 6587. American
    Association for the Advancement of Science, pp. 1385–1389, 2022.
  ista: Su L, Wang D, Wang S, Qin B, Wang Y, Qin Y, Jin Y, Chang C, Zhao LD. 2022.
    High thermoelectric performance realized through manipulating layered phonon-electron
    decoupling. Science. 375(6587), 1385–1389.
  mla: Su, Lizhong, et al. “High Thermoelectric Performance Realized through Manipulating
    Layered Phonon-Electron Decoupling.” <i>Science</i>, vol. 375, no. 6587, American
    Association for the Advancement of Science, 2022, pp. 1385–89, doi:<a href="https://doi.org/10.1126/science.abn8997">10.1126/science.abn8997</a>.
  short: L. Su, D. Wang, S. Wang, B. Qin, Y. Wang, Y. Qin, Y. Jin, C. Chang, L.D.
    Zhao, Science 375 (2022) 1385–1389.
date_created: 2022-04-10T22:01:40Z
date_published: 2022-03-25T00:00:00Z
date_updated: 2023-10-16T09:10:36Z
day: '25'
department:
- _id: MaIb
doi: 10.1126/science.abn8997
external_id:
  isi:
  - '000778894800038'
  pmid:
  - '35324303'
intvolume: '       375'
isi: 1
issue: '6587'
language:
- iso: eng
month: '03'
oa_version: None
page: 1385-1389
pmid: 1
project:
- _id: 9B8804FC-BA93-11EA-9121-9846C619BF3A
  grant_number: M02889
  name: Bottom-up Engineering for Thermoelectric Applications
publication: Science
publication_identifier:
  eissn:
  - 1095-9203
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: High thermoelectric performance realized through manipulating layered phonon-electron
  decoupling
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 375
year: '2022'
...
---
_id: '11145'
abstract:
- lang: eng
  text: List-decodability of Reed-Solomon codes has re-ceived a lot of attention,
    but the best-possible dependence between the parameters is still not well-understood.
    In this work, we focus on the case where the list-decoding radius is of the form
    r=1−ε for ε tending to zero. Our main result states that there exist Reed-Solomon
    codes with rate Ω(ε) which are (1−ε,O(1/ε) -list-decodable, meaning that any Hamming
    ball of radius 1−ε contains at most O(1/ε) codewords. This trade-off between rate
    and list-decoding radius is best-possible for any code with list size less than
    exponential in the block length. By achieving this trade-off between rate and
    list-decoding radius we improve a recent result of Guo, Li, Shangguan, Tamo, and
    Wootters, and resolve the main motivating question of their work. Moreover, while
    their result requires the field to be exponentially large in the block length,
    we only need the field size to be polynomially large (and in fact, almost-linear
    suffices). We deduce our main result from a more general theorem, in which we
    prove good list-decodability properties of random puncturings of any given code
    with very large distance.
article_processing_charge: No
arxiv: 1
author:
- first_name: Asaf
  full_name: Ferber, Asaf
  last_name: Ferber
- first_name: Matthew Alan
  full_name: Kwan, Matthew Alan
  id: 5fca0887-a1db-11eb-95d1-ca9d5e0453b3
  last_name: Kwan
  orcid: 0000-0002-4003-7567
- first_name: Lisa
  full_name: Sauermann, Lisa
  last_name: Sauermann
citation:
  ama: 'Ferber A, Kwan MA, Sauermann L. List-decodability with large radius for Reed-Solomon
    codes. In: <i>62nd Annual IEEE Symposium on Foundations of Computer Science</i>.
    Vol 2022. IEEE; 2022:720-726. doi:<a href="https://doi.org/10.1109/FOCS52979.2021.00075">10.1109/FOCS52979.2021.00075</a>'
  apa: 'Ferber, A., Kwan, M. A., &#38; Sauermann, L. (2022). List-decodability with
    large radius for Reed-Solomon codes. In <i>62nd Annual IEEE Symposium on Foundations
    of Computer Science</i> (Vol. 2022, pp. 720–726). Denver, CO, United States: IEEE.
    <a href="https://doi.org/10.1109/FOCS52979.2021.00075">https://doi.org/10.1109/FOCS52979.2021.00075</a>'
  chicago: Ferber, Asaf, Matthew Alan Kwan, and Lisa Sauermann. “List-Decodability
    with Large Radius for Reed-Solomon Codes.” In <i>62nd Annual IEEE Symposium on
    Foundations of Computer Science</i>, 2022:720–26. IEEE, 2022. <a href="https://doi.org/10.1109/FOCS52979.2021.00075">https://doi.org/10.1109/FOCS52979.2021.00075</a>.
  ieee: A. Ferber, M. A. Kwan, and L. Sauermann, “List-decodability with large radius
    for Reed-Solomon codes,” in <i>62nd Annual IEEE Symposium on Foundations of Computer
    Science</i>, Denver, CO, United States, 2022, vol. 2022, pp. 720–726.
  ista: 'Ferber A, Kwan MA, Sauermann L. 2022. List-decodability with large radius
    for Reed-Solomon codes. 62nd Annual IEEE Symposium on Foundations of Computer
    Science. FOCS: Symposium on Foundations of Computer Science vol. 2022, 720–726.'
  mla: Ferber, Asaf, et al. “List-Decodability with Large Radius for Reed-Solomon
    Codes.” <i>62nd Annual IEEE Symposium on Foundations of Computer Science</i>,
    vol. 2022, IEEE, 2022, pp. 720–26, doi:<a href="https://doi.org/10.1109/FOCS52979.2021.00075">10.1109/FOCS52979.2021.00075</a>.
  short: A. Ferber, M.A. Kwan, L. Sauermann, in:, 62nd Annual IEEE Symposium on Foundations
    of Computer Science, IEEE, 2022, pp. 720–726.
conference:
  end_date: 2022-02-10
  location: Denver, CO, United States
  name: 'FOCS: Symposium on Foundations of Computer Science'
  start_date: 2022-02-07
date_created: 2022-04-10T22:01:40Z
date_published: 2022-02-01T00:00:00Z
date_updated: 2023-08-03T06:57:02Z
day: '01'
department:
- _id: MaKw
doi: 10.1109/FOCS52979.2021.00075
external_id:
  arxiv:
  - '2012.10584'
  isi:
  - '000802209600065'
intvolume: '      2022'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: ' https://doi.org/10.48550/arXiv.2012.10584'
month: '02'
oa: 1
oa_version: Preprint
page: 720-726
publication: 62nd Annual IEEE Symposium on Foundations of Computer Science
publication_identifier:
  isbn:
  - '9781665420556'
  issn:
  - 0272-5428
publication_status: published
publisher: IEEE
quality_controlled: '1'
related_material:
  record:
  - id: '10775'
    relation: later_version
    status: public
scopus_import: '1'
status: public
title: List-decodability with large radius for Reed-Solomon codes
type: conference
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 2022
year: '2022'
...
---
_id: '11155'
abstract:
- lang: eng
  text: The potential of energy filtering and direct electron detection for cryo-electron
    microscopy (cryo-EM) has been well documented. Here, we assess the performance
    of recently introduced hardware for cryo-electron tomography (cryo-ET) and subtomogram
    averaging (STA), an increasingly popular structural determination method for complex
    3D specimens. We acquired cryo-ET datasets of EIAV virus-like particles (VLPs)
    on two contemporary cryo-EM systems equipped with different energy filters and
    direct electron detectors (DED), specifically a Krios G4, equipped with a cold
    field emission gun (CFEG), Thermo Fisher Scientific Selectris X energy filter,
    and a Falcon 4 DED; and a Krios G3i, with a Schottky field emission gun (XFEG),
    a Gatan Bioquantum energy filter, and a K3 DED. We performed constrained cross-correlation-based
    STA on equally sized datasets acquired on the respective systems. The resulting
    EIAV CA hexamer reconstructions show that both systems perform comparably in the
    4–6 Å resolution range based on Fourier-Shell correlation (FSC). In addition,
    by employing a recently introduced multiparticle refinement approach, we obtained
    a reconstruction of the EIAV CA hexamer at 2.9 Å. Our results demonstrate the
    potential of the new generation of energy filters and DEDs for STA, and the effects
    of using different processing pipelines on their STA outcomes.
acknowledged_ssus:
- _id: LifeSc
- _id: ScienComp
- _id: EM-Fac
acknowledgement: This work was funded by the Austrian Science Fund (FWF) grant P31445
  to F.K.M.S and the National Institute of Allergy and Infectious Diseases under awards
  R01AI147890 to R.A.D. This research was also supported by the Scientific Service
  Units (SSUs) of IST Austria through resources provided by Scientific Computing (SciComp),
  the Life Science Facility (LSF), and the Electron Microscopy Facility (EMF). We
  thank Dustin Morado for providing the software SubTOM for data processing. We also
  thank William Wan for critical reading of the manuscript and valuable feedback.
article_number: '107852'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Martin
  full_name: Obr, Martin
  id: 4741CA5A-F248-11E8-B48F-1D18A9856A87
  last_name: Obr
- first_name: Wim J.H.
  full_name: Hagen, Wim J.H.
  last_name: Hagen
- first_name: Robert A.
  full_name: Dick, Robert A.
  last_name: Dick
- first_name: Lingbo
  full_name: Yu, Lingbo
  last_name: Yu
- first_name: Abhay
  full_name: Kotecha, Abhay
  last_name: Kotecha
- first_name: Florian KM
  full_name: Schur, Florian KM
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
citation:
  ama: Obr M, Hagen WJH, Dick RA, Yu L, Kotecha A, Schur FK. Exploring high-resolution
    cryo-ET and subtomogram averaging capabilities of contemporary DEDs. <i>Journal
    of Structural Biology</i>. 2022;214(2). doi:<a href="https://doi.org/10.1016/j.jsb.2022.107852">10.1016/j.jsb.2022.107852</a>
  apa: Obr, M., Hagen, W. J. H., Dick, R. A., Yu, L., Kotecha, A., &#38; Schur, F.
    K. (2022). Exploring high-resolution cryo-ET and subtomogram averaging capabilities
    of contemporary DEDs. <i>Journal of Structural Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.jsb.2022.107852">https://doi.org/10.1016/j.jsb.2022.107852</a>
  chicago: Obr, Martin, Wim J.H. Hagen, Robert A. Dick, Lingbo Yu, Abhay Kotecha,
    and Florian KM Schur. “Exploring High-Resolution Cryo-ET and Subtomogram Averaging
    Capabilities of Contemporary DEDs.” <i>Journal of Structural Biology</i>. Elsevier,
    2022. <a href="https://doi.org/10.1016/j.jsb.2022.107852">https://doi.org/10.1016/j.jsb.2022.107852</a>.
  ieee: M. Obr, W. J. H. Hagen, R. A. Dick, L. Yu, A. Kotecha, and F. K. Schur, “Exploring
    high-resolution cryo-ET and subtomogram averaging capabilities of contemporary
    DEDs,” <i>Journal of Structural Biology</i>, vol. 214, no. 2. Elsevier, 2022.
  ista: Obr M, Hagen WJH, Dick RA, Yu L, Kotecha A, Schur FK. 2022. Exploring high-resolution
    cryo-ET and subtomogram averaging capabilities of contemporary DEDs. Journal of
    Structural Biology. 214(2), 107852.
  mla: Obr, Martin, et al. “Exploring High-Resolution Cryo-ET and Subtomogram Averaging
    Capabilities of Contemporary DEDs.” <i>Journal of Structural Biology</i>, vol.
    214, no. 2, 107852, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.jsb.2022.107852">10.1016/j.jsb.2022.107852</a>.
  short: M. Obr, W.J.H. Hagen, R.A. Dick, L. Yu, A. Kotecha, F.K. Schur, Journal of
    Structural Biology 214 (2022).
date_created: 2022-04-15T07:10:26Z
date_published: 2022-06-01T00:00:00Z
date_updated: 2023-08-03T06:25:23Z
day: '01'
ddc:
- '570'
department:
- _id: FlSc
doi: 10.1016/j.jsb.2022.107852
external_id:
  isi:
  - '000790733600001'
  pmid:
  - '35351542'
file:
- access_level: open_access
  checksum: 0b1eb53447aae8e95ae4c12d193b0b00
  content_type: application/pdf
  creator: dernst
  date_created: 2022-08-02T11:07:58Z
  date_updated: 2022-08-02T11:07:58Z
  file_id: '11722'
  file_name: 2022_JourStructuralBiology_Obr.pdf
  file_size: 7080863
  relation: main_file
  success: 1
file_date_updated: 2022-08-02T11:07:58Z
has_accepted_license: '1'
intvolume: '       214'
isi: 1
issue: '2'
keyword:
- Structural Biology
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 26736D6A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P31445
  name: Structural conservation and diversity in retroviral capsid
publication: Journal of Structural Biology
publication_identifier:
  issn:
  - 1047-8477
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Exploring high-resolution cryo-ET and subtomogram averaging capabilities of
  contemporary DEDs
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 214
year: '2022'
...
---
_id: '11160'
abstract:
- lang: eng
  text: Mutations in the chromodomain helicase DNA-binding 8 (CHD8) gene are a frequent
    cause of autism spectrum disorder (ASD). While its phenotypic spectrum often encompasses
    macrocephaly, implicating cortical abnormalities, how CHD8 haploinsufficiency
    affects neurodevelopmental is unclear. Here, employing human cerebral organoids,
    we find that CHD8 haploinsufficiency disrupted neurodevelopmental trajectories
    with an accelerated and delayed generation of, respectively, inhibitory and excitatory
    neurons that yields, at days 60 and 120, symmetrically opposite expansions in
    their proportions. This imbalance is consistent with an enlargement of cerebral
    organoids as an in vitro correlate of patients’ macrocephaly. Through an isogenic
    design of patient-specific mutations and mosaic organoids, we define genotype-phenotype
    relationships and uncover their cell-autonomous nature. Our results define cell-type-specific
    CHD8-dependent molecular defects related to an abnormal program of proliferation
    and alternative splicing. By identifying cell-type-specific effects of CHD8 mutations,
    our study uncovers reproducible developmental alterations that may be employed
    for neurodevelopmental disease modeling.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
acknowledgement: We thank Farnaz Freeman for technical assistance. This research was
  supported by the Scientific Service Units (SSU) of IST Austria through resources
  provided by the Bioimaging Facility (BIF) and the Life Science Facility (LSF). This
  work supported by the European Union’s Horizon 2020 research and innovation program
  (ERC) grant 715508 to G.N. (REVERSEAUTISM) and grant 825759 to G.T. (ENDpoiNTs);
  the Fondazione Cariplo 2017-0886 to A.L.T.; E-Rare-3 JTC 2018 IMPACT to M. Gabriele;
  and the Austrian Science Fund FWF I 4205-B to G.N. Graphical abstract and figures
  were created using BioRender.com.
article_number: '110615'
article_processing_charge: Yes
article_type: original
author:
- first_name: Carlo Emanuele
  full_name: Villa, Carlo Emanuele
  last_name: Villa
- first_name: Cristina
  full_name: Cheroni, Cristina
  last_name: Cheroni
- first_name: Christoph
  full_name: Dotter, Christoph
  id: 4C66542E-F248-11E8-B48F-1D18A9856A87
  last_name: Dotter
  orcid: 0000-0002-9033-9096
- first_name: Alejandro
  full_name: López-Tóbon, Alejandro
  last_name: López-Tóbon
- first_name: Bárbara
  full_name: Oliveira, Bárbara
  id: 3B03AA1A-F248-11E8-B48F-1D18A9856A87
  last_name: Oliveira
- first_name: Roberto
  full_name: Sacco, Roberto
  id: 42C9F57E-F248-11E8-B48F-1D18A9856A87
  last_name: Sacco
- first_name: Aysan Çerağ
  full_name: Yahya, Aysan Çerağ
  id: 365A65F8-F248-11E8-B48F-1D18A9856A87
  last_name: Yahya
- first_name: Jasmin
  full_name: Morandell, Jasmin
  id: 4739D480-F248-11E8-B48F-1D18A9856A87
  last_name: Morandell
- first_name: Michele
  full_name: Gabriele, Michele
  last_name: Gabriele
- first_name: Mojtaba
  full_name: Tavakoli, Mojtaba
  id: 3A0A06F4-F248-11E8-B48F-1D18A9856A87
  last_name: Tavakoli
  orcid: 0000-0002-7667-6854
- first_name: Julia
  full_name: Lyudchik, Julia
  id: 46E28B80-F248-11E8-B48F-1D18A9856A87
  last_name: Lyudchik
- first_name: Christoph M
  full_name: Sommer, Christoph M
  id: 4DF26D8C-F248-11E8-B48F-1D18A9856A87
  last_name: Sommer
  orcid: 0000-0003-1216-9105
- first_name: Mariano
  full_name: Gabitto, Mariano
  last_name: Gabitto
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
- first_name: Giuseppe
  full_name: Testa, Giuseppe
  last_name: Testa
- first_name: Gaia
  full_name: Novarino, Gaia
  id: 3E57A680-F248-11E8-B48F-1D18A9856A87
  last_name: Novarino
  orcid: 0000-0002-7673-7178
citation:
  ama: Villa CE, Cheroni C, Dotter C, et al. CHD8 haploinsufficiency links autism
    to transient alterations in excitatory and inhibitory trajectories. <i>Cell Reports</i>.
    2022;39(1). doi:<a href="https://doi.org/10.1016/j.celrep.2022.110615">10.1016/j.celrep.2022.110615</a>
  apa: Villa, C. E., Cheroni, C., Dotter, C., López-Tóbon, A., Oliveira, B., Sacco,
    R., … Novarino, G. (2022). CHD8 haploinsufficiency links autism to transient alterations
    in excitatory and inhibitory trajectories. <i>Cell Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2022.110615">https://doi.org/10.1016/j.celrep.2022.110615</a>
  chicago: Villa, Carlo Emanuele, Cristina Cheroni, Christoph Dotter, Alejandro López-Tóbon,
    Bárbara Oliveira, Roberto Sacco, Aysan Çerağ Yahya, et al. “CHD8 Haploinsufficiency
    Links Autism to Transient Alterations in Excitatory and Inhibitory Trajectories.”
    <i>Cell Reports</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.celrep.2022.110615">https://doi.org/10.1016/j.celrep.2022.110615</a>.
  ieee: C. E. Villa <i>et al.</i>, “CHD8 haploinsufficiency links autism to transient
    alterations in excitatory and inhibitory trajectories,” <i>Cell Reports</i>, vol.
    39, no. 1. Elsevier, 2022.
  ista: Villa CE, Cheroni C, Dotter C, López-Tóbon A, Oliveira B, Sacco R, Yahya AÇ,
    Morandell J, Gabriele M, Tavakoli M, Lyudchik J, Sommer CM, Gabitto M, Danzl JG,
    Testa G, Novarino G. 2022. CHD8 haploinsufficiency links autism to transient alterations
    in excitatory and inhibitory trajectories. Cell Reports. 39(1), 110615.
  mla: Villa, Carlo Emanuele, et al. “CHD8 Haploinsufficiency Links Autism to Transient
    Alterations in Excitatory and Inhibitory Trajectories.” <i>Cell Reports</i>, vol.
    39, no. 1, 110615, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.celrep.2022.110615">10.1016/j.celrep.2022.110615</a>.
  short: C.E. Villa, C. Cheroni, C. Dotter, A. López-Tóbon, B. Oliveira, R. Sacco,
    A.Ç. Yahya, J. Morandell, M. Gabriele, M. Tavakoli, J. Lyudchik, C.M. Sommer,
    M. Gabitto, J.G. Danzl, G. Testa, G. Novarino, Cell Reports 39 (2022).
date_created: 2022-04-15T09:03:10Z
date_published: 2022-04-05T00:00:00Z
date_updated: 2024-03-25T23:30:25Z
day: '05'
ddc:
- '570'
department:
- _id: JoDa
- _id: GaNo
doi: 10.1016/j.celrep.2022.110615
ec_funded: 1
external_id:
  isi:
  - '000785983900003'
  pmid:
  - '35385734'
file:
- access_level: open_access
  checksum: b4e8d68f0268dec499af333e6fd5d8e1
  content_type: application/pdf
  creator: dernst
  date_created: 2022-04-15T09:06:25Z
  date_updated: 2022-04-15T09:06:25Z
  file_id: '11164'
  file_name: 2022_CellReports_Villa.pdf
  file_size: '7808644'
  relation: main_file
  success: 1
file_date_updated: 2022-04-15T09:06:25Z
has_accepted_license: '1'
intvolume: '        39'
isi: 1
issue: '1'
keyword:
- General Biochemistry
- Genetics and Molecular Biology
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 25444568-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715508'
  name: Probing the Reversibility of Autism Spectrum Disorders by Employing in vivo
    and in vitro Models
- _id: 2690FEAC-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I04205
  name: Identification of converging Molecular Pathways Across Chromatinopathies as
    Targets for Therapy
publication: Cell Reports
publication_identifier:
  issn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  record:
  - id: '12364'
    relation: dissertation_contains
    status: public
status: public
title: CHD8 haploinsufficiency links autism to transient alterations in excitatory
  and inhibitory trajectories
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 39
year: '2022'
...
---
_id: '11167'
abstract:
- lang: eng
  text: Complex I is one of the major respiratory complexes, conserved from bacteria
    to mammals. It oxidises NADH, reduces quinone and pumps protons across the membrane,
    thus playing a central role in the oxidative energy metabolism. In this review
    we discuss our current state of understanding the structure of complex I from
    various species of mammals, plants, fungi, and bacteria, as well as of several
    complex I-related proteins. By comparing the structural evidence from these systems
    in different redox states and data from mutagenesis and molecular simulations,
    we formulate the mechanisms of electron transfer and proton pumping and explain
    how they are conformationally and electrostatically coupled. Finally, we discuss
    the structural basis of the deactivation phenomenon in mammalian complex I.
article_number: '102350'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Domen
  full_name: Kampjut, Domen
  id: 37233050-F248-11E8-B48F-1D18A9856A87
  last_name: Kampjut
- first_name: Leonid A
  full_name: Sazanov, Leonid A
  id: 338D39FE-F248-11E8-B48F-1D18A9856A87
  last_name: Sazanov
  orcid: 0000-0002-0977-7989
citation:
  ama: Kampjut D, Sazanov LA. Structure of respiratory complex I – An emerging blueprint
    for the mechanism. <i>Current Opinion in Structural Biology</i>. 2022;74. doi:<a
    href="https://doi.org/10.1016/j.sbi.2022.102350">10.1016/j.sbi.2022.102350</a>
  apa: Kampjut, D., &#38; Sazanov, L. A. (2022). Structure of respiratory complex
    I – An emerging blueprint for the mechanism. <i>Current Opinion in Structural
    Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.sbi.2022.102350">https://doi.org/10.1016/j.sbi.2022.102350</a>
  chicago: Kampjut, Domen, and Leonid A Sazanov. “Structure of Respiratory Complex
    I – An Emerging Blueprint for the Mechanism.” <i>Current Opinion in Structural
    Biology</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.sbi.2022.102350">https://doi.org/10.1016/j.sbi.2022.102350</a>.
  ieee: D. Kampjut and L. A. Sazanov, “Structure of respiratory complex I – An emerging
    blueprint for the mechanism,” <i>Current Opinion in Structural Biology</i>, vol.
    74. Elsevier, 2022.
  ista: Kampjut D, Sazanov LA. 2022. Structure of respiratory complex I – An emerging
    blueprint for the mechanism. Current Opinion in Structural Biology. 74, 102350.
  mla: Kampjut, Domen, and Leonid A. Sazanov. “Structure of Respiratory Complex I
    – An Emerging Blueprint for the Mechanism.” <i>Current Opinion in Structural Biology</i>,
    vol. 74, 102350, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.sbi.2022.102350">10.1016/j.sbi.2022.102350</a>.
  short: D. Kampjut, L.A. Sazanov, Current Opinion in Structural Biology 74 (2022).
date_created: 2022-04-15T09:32:35Z
date_published: 2022-06-01T00:00:00Z
date_updated: 2023-08-03T06:31:06Z
day: '01'
ddc:
- '570'
department:
- _id: LeSa
doi: 10.1016/j.sbi.2022.102350
external_id:
  isi:
  - '000829029500020'
  pmid:
  - '35316665'
file:
- access_level: open_access
  checksum: 72bdde48853643a32d42b75f54965c44
  content_type: application/pdf
  creator: dernst
  date_created: 2022-08-05T05:56:03Z
  date_updated: 2022-08-05T05:56:03Z
  file_id: '11725'
  file_name: 2022_CurrentOpStructBiology_Kampjut.pdf
  file_size: 815607
  relation: main_file
  success: 1
file_date_updated: 2022-08-05T05:56:03Z
has_accepted_license: '1'
intvolume: '        74'
isi: 1
keyword:
- Molecular Biology
- Structural Biology
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: Current Opinion in Structural Biology
publication_identifier:
  issn:
  - 0959-440X
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Structure of respiratory complex I – An emerging blueprint for the mechanism
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 74
year: '2022'
...
---
_id: '11179'
abstract:
- lang: eng
  text: Large oligomeric enzymes control a myriad of cellular processes, from protein
    synthesis and degradation to metabolism. The 0.5 MDa large TET2 aminopeptidase,
    a prototypical protease important for cellular homeostasis, degrades peptides
    within a ca. 60 Å wide tetrahedral chamber with four lateral openings. The mechanisms
    of substrate trafficking and processing remain debated. Here, we integrate magic-angle
    spinning (MAS) NMR, mutagenesis, co-evolution analysis and molecular dynamics
    simulations and reveal that a loop in the catalytic chamber is a key element for
    enzymatic function. The loop is able to stabilize ligands in the active site and
    may additionally have a direct role in activating the catalytic water molecule
    whereby a conserved histidine plays a key role. Our data provide a strong case
    for the functional importance of highly dynamic - and often overlooked - parts
    of an enzyme, and the potential of MAS NMR to investigate their dynamics at atomic
    resolution.
acknowledgement: "We are grateful to Bernhard Brutscher, Alicia Vallet, and Adrien
  Favier for excellent NMR\r\nplatform operation and management. The plasmid coding
  for TET2 was kindly provided\r\nby Bruno Franzetti and Jerome Boisbouvier (IBS Grenoble).
  We thank Anne-Marie Villard\r\nand the RoBioMol platform for preparing the loop
  deletion construct. The RoBioMol\r\nplatform is part of the Grenoble Instruct-ERIC
  center (ISBG; UAR 3518 CNRS-CEAUGA-EMBL) within the Grenoble Partnership for Structural
  Biology (PSB), supported by FRISBI (ANR-10-INBS-0005-02) and GRAL (ANR-10-LABX-49-01),
  financed within the University Grenoble Alpes graduate school (Ecoles Universitaires
  de Recherche) CBHEUR-GS (ANR-17-EURE-0003). This work was supported by the European
  Research Council (StG-2012-311318-ProtDyn2Function to P. S.) and the French Agence
  Nationale de la Recherche (ANR), under grant ANR-14-ACHN-0016 (M.P. and A.B.)."
article_number: '1927'
article_processing_charge: No
article_type: original
author:
- first_name: Diego F.
  full_name: Gauto, Diego F.
  last_name: Gauto
- first_name: Pavel
  full_name: Macek, Pavel
  last_name: Macek
- first_name: Duccio
  full_name: Malinverni, Duccio
  last_name: Malinverni
- first_name: Hugo
  full_name: Fraga, Hugo
  last_name: Fraga
- first_name: Matteo
  full_name: Paloni, Matteo
  last_name: Paloni
- first_name: Iva
  full_name: Sučec, Iva
  last_name: Sučec
- first_name: Audrey
  full_name: Hessel, Audrey
  last_name: Hessel
- first_name: Juan Pablo
  full_name: Bustamante, Juan Pablo
  last_name: Bustamante
- first_name: Alessandro
  full_name: Barducci, Alessandro
  last_name: Barducci
- first_name: Paul
  full_name: Schanda, Paul
  id: 7B541462-FAF6-11E9-A490-E8DFE5697425
  last_name: Schanda
  orcid: 0000-0002-9350-7606
citation:
  ama: Gauto DF, Macek P, Malinverni D, et al. Functional control of a 0.5 MDa TET
    aminopeptidase by a flexible loop revealed by MAS NMR. <i>Nature Communications</i>.
    2022;13. doi:<a href="https://doi.org/10.1038/s41467-022-29423-0">10.1038/s41467-022-29423-0</a>
  apa: Gauto, D. F., Macek, P., Malinverni, D., Fraga, H., Paloni, M., Sučec, I.,
    … Schanda, P. (2022). Functional control of a 0.5 MDa TET aminopeptidase by a
    flexible loop revealed by MAS NMR. <i>Nature Communications</i>. Springer Nature.
    <a href="https://doi.org/10.1038/s41467-022-29423-0">https://doi.org/10.1038/s41467-022-29423-0</a>
  chicago: Gauto, Diego F., Pavel Macek, Duccio Malinverni, Hugo Fraga, Matteo Paloni,
    Iva Sučec, Audrey Hessel, Juan Pablo Bustamante, Alessandro Barducci, and Paul
    Schanda. “Functional Control of a 0.5 MDa TET Aminopeptidase by a Flexible Loop
    Revealed by MAS NMR.” <i>Nature Communications</i>. Springer Nature, 2022. <a
    href="https://doi.org/10.1038/s41467-022-29423-0">https://doi.org/10.1038/s41467-022-29423-0</a>.
  ieee: D. F. Gauto <i>et al.</i>, “Functional control of a 0.5 MDa TET aminopeptidase
    by a flexible loop revealed by MAS NMR,” <i>Nature Communications</i>, vol. 13.
    Springer Nature, 2022.
  ista: Gauto DF, Macek P, Malinverni D, Fraga H, Paloni M, Sučec I, Hessel A, Bustamante
    JP, Barducci A, Schanda P. 2022. Functional control of a 0.5 MDa TET aminopeptidase
    by a flexible loop revealed by MAS NMR. Nature Communications. 13, 1927.
  mla: Gauto, Diego F., et al. “Functional Control of a 0.5 MDa TET Aminopeptidase
    by a Flexible Loop Revealed by MAS NMR.” <i>Nature Communications</i>, vol. 13,
    1927, Springer Nature, 2022, doi:<a href="https://doi.org/10.1038/s41467-022-29423-0">10.1038/s41467-022-29423-0</a>.
  short: D.F. Gauto, P. Macek, D. Malinverni, H. Fraga, M. Paloni, I. Sučec, A. Hessel,
    J.P. Bustamante, A. Barducci, P. Schanda, Nature Communications 13 (2022).
date_created: 2022-04-17T22:01:45Z
date_published: 2022-04-08T00:00:00Z
date_updated: 2023-08-03T06:54:56Z
day: '08'
ddc:
- '570'
department:
- _id: PaSc
doi: 10.1038/s41467-022-29423-0
external_id:
  isi:
  - '000781498700009'
file:
- access_level: open_access
  checksum: db61d5534e988743d6266d3675d77b08
  content_type: application/pdf
  creator: dernst
  date_created: 2022-05-02T08:48:00Z
  date_updated: 2022-05-02T08:48:00Z
  file_id: '11348'
  file_name: 2022_NatureCommunications_Gauto.pdf
  file_size: 2637590
  relation: main_file
  success: 1
file_date_updated: 2022-05-02T08:48:00Z
has_accepted_license: '1'
intvolume: '        13'
isi: 1
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
publication: Nature Communications
publication_identifier:
  eissn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: https://doi.org/10.1038/s41467-022-31243-1
scopus_import: '1'
status: public
title: Functional control of a 0.5 MDa TET aminopeptidase by a flexible loop revealed
  by MAS NMR
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 13
year: '2022'
...
---
_id: '11180'
abstract:
- lang: eng
  text: "Designing and implementing efficient parallel priority schedulers is an active
    research area. An intriguing proposed design is the Multi-Queue: given n threads
    and m ≥ n distinct priority queues, task insertions are performed uniformly at
    random, while, to delete, a thread picks two queues uniformly at random, and removes
    the observed task of higher priority. This approach scales well, and has probabilistic
    rank guarantees: roughly, the rank of each task removed, relative to remaining
    tasks in all other queues, is O (m) in expectation. Yet, the performance of this
    pattern is below that of well-engineered schedulers, which eschew theoretical
    guarantees for practical efficiency.\r\n\r\nWe investigate whether it is possible
    to design and implement a Multi-Queue-based task scheduler that is both highly-efficient
    and has analytical guarantees. We propose a new variant called the Stealing Multi-Queue
    (SMQ), a cache-efficient variant of the Multi-Queue, which leverages both queue
    affinity---each thread has a local queue, from which tasks are usually removed;
    but, with some probability, threads also attempt to steal higher-priority tasks
    from the other queues---and task batching, that is, the processing of several
    tasks in a single insert / remove step. These ideas are well-known for task scheduling
    without priorities; our theoretical contribution is showing that, despite relaxations,
    this design can still provide rank guarantees, which in turn implies bounds on
    total work performed. We provide a general SMQ implementation which can surpass
    state-of-the-art schedulers such as OBIM and PMOD in terms of performance on popular
    graph-processing benchmarks. Notably, the performance improvement comes mainly
    from the superior rank guarantees provided by our scheduler, confirming that analytically-reasoned
    approaches can still provide performance improvements for priority task scheduling."
acknowledgement: We would like to thank the anonymous reviewers for their useful comments.
  This project has received funding from the European Research Council (ERC) under
  the European Union’s Horizon 2020 research and innovation programme (grant agreement
  No 805223 ScaleML).
article_processing_charge: No
arxiv: 1
author:
- first_name: Anastasiia
  full_name: Postnikova, Anastasiia
  last_name: Postnikova
- first_name: Nikita
  full_name: Koval, Nikita
  id: 2F4DB10C-F248-11E8-B48F-1D18A9856A87
  last_name: Koval
- first_name: Giorgi
  full_name: Nadiradze, Giorgi
  id: 3279A00C-F248-11E8-B48F-1D18A9856A87
  last_name: Nadiradze
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
citation:
  ama: 'Postnikova A, Koval N, Nadiradze G, Alistarh D-A. Multi-queues can be state-of-the-art
    priority schedulers. In: <i>Proceedings of the 27th ACM SIGPLAN Symposium on Principles
    and Practice of Parallel Programming</i>. Association for Computing Machinery;
    2022:353-367. doi:<a href="https://doi.org/10.1145/3503221.3508432">10.1145/3503221.3508432</a>'
  apa: 'Postnikova, A., Koval, N., Nadiradze, G., &#38; Alistarh, D.-A. (2022). Multi-queues
    can be state-of-the-art priority schedulers. In <i>Proceedings of the 27th ACM
    SIGPLAN Symposium on Principles and Practice of Parallel Programming</i> (pp.
    353–367). Seoul, Republic of Korea: Association for Computing Machinery. <a href="https://doi.org/10.1145/3503221.3508432">https://doi.org/10.1145/3503221.3508432</a>'
  chicago: Postnikova, Anastasiia, Nikita Koval, Giorgi Nadiradze, and Dan-Adrian
    Alistarh. “Multi-Queues Can Be State-of-the-Art Priority Schedulers.” In <i>Proceedings
    of the 27th ACM SIGPLAN Symposium on Principles and Practice of Parallel Programming</i>,
    353–67. Association for Computing Machinery, 2022. <a href="https://doi.org/10.1145/3503221.3508432">https://doi.org/10.1145/3503221.3508432</a>.
  ieee: A. Postnikova, N. Koval, G. Nadiradze, and D.-A. Alistarh, “Multi-queues can
    be state-of-the-art priority schedulers,” in <i>Proceedings of the 27th ACM SIGPLAN
    Symposium on Principles and Practice of Parallel Programming</i>, Seoul, Republic
    of Korea, 2022, pp. 353–367.
  ista: 'Postnikova A, Koval N, Nadiradze G, Alistarh D-A. 2022. Multi-queues can
    be state-of-the-art priority schedulers. Proceedings of the 27th ACM SIGPLAN Symposium
    on Principles and Practice of Parallel Programming. PPoPP: Sympopsium on Principles
    and Practice of Parallel Programming, 353–367.'
  mla: Postnikova, Anastasiia, et al. “Multi-Queues Can Be State-of-the-Art Priority
    Schedulers.” <i>Proceedings of the 27th ACM SIGPLAN Symposium on Principles and
    Practice of Parallel Programming</i>, Association for Computing Machinery, 2022,
    pp. 353–67, doi:<a href="https://doi.org/10.1145/3503221.3508432">10.1145/3503221.3508432</a>.
  short: A. Postnikova, N. Koval, G. Nadiradze, D.-A. Alistarh, in:, Proceedings of
    the 27th ACM SIGPLAN Symposium on Principles and Practice of Parallel Programming,
    Association for Computing Machinery, 2022, pp. 353–367.
conference:
  end_date: 2022-04-06
  location: Seoul, Republic of Korea
  name: 'PPoPP: Sympopsium on Principles and Practice of Parallel Programming'
  start_date: 2022-04-02
date_created: 2022-04-17T22:01:46Z
date_published: 2022-04-02T00:00:00Z
date_updated: 2023-08-03T06:48:35Z
day: '02'
department:
- _id: DaAl
doi: 10.1145/3503221.3508432
ec_funded: 1
external_id:
  arxiv:
  - '2109.00657'
  isi:
  - '000883318200025'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: ' https://doi.org/10.48550/arXiv.2109.00657'
month: '04'
oa: 1
oa_version: Preprint
page: 353-367
project:
- _id: 268A44D6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '805223'
  name: Elastic Coordination for Scalable Machine Learning
publication: Proceedings of the 27th ACM SIGPLAN Symposium on Principles and Practice
  of Parallel Programming
publication_identifier:
  isbn:
  - '9781450392044'
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
related_material:
  record:
  - id: '13076'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Multi-queues can be state-of-the-art priority schedulers
type: conference
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
year: '2022'
...
---
_id: '11181'
abstract:
- lang: eng
  text: 'To maximize the performance of concurrent data structures, researchers have
    often turned to highly complex fine-grained techniques, resulting in efficient
    and elegant algorithms, which can however be often difficult to understand and
    prove correct. While simpler techniques exist, such as transactional memory, they
    can have limited performance or portability relative to their fine-grained counterparts.
    Approaches at both ends of this complexity-performance spectrum have been extensively
    explored, but relatively less is known about the middle ground: approaches that
    are willing to sacrifice some performance for simplicity, while remaining competitive
    with state-of-the-art handcrafted designs. In this paper, we explore this middle
    ground, and present PathCAS, a primitive that combines ideas from multi-word CAS
    (KCAS) and transactional memory approaches, while carefully avoiding overhead.
    We show how PathCAS can be used to implement efficient search data structures
    relatively simply, using an internal binary search tree as an example, then extending
    this to an AVL tree. Our best implementations outperform many handcrafted search
    trees: in search-heavy workloads, it rivals the BCCO tree [5], the fastest known
    concurrent binary tree in terms of search performance [3]. Our results suggest
    that PathCAS can yield concurrent data structures that are relatively easy to
    build and prove correct, while offering surprisingly high performance.'
acknowledgement: "This work was supported by: the Natural Sciences and Engineering
  Research Council of Canada (NSERC) Collaborative Research and Development grant:
  CRDPJ 539431-19, the\r\nCanada Foundation for Innovation John R. Evans Leaders Fund
  with equal support from the Ontario Research Fund CFI Leaders Opportunity Fund:
  38512, Waterloo Huawei Joint Innovation Lab project “Scalable Infrastructure for
  Next Generation Data Management Systems”, NSERC Discovery Launch Supplement: DGECR-2019-00048,
  NSERC Discovery\r\nProgram under the grants: RGPIN-2019-04227 and RGPIN04512-2018,
  and the University of Waterloo. We would also like to thank the reviewers for their
  insightful comments."
article_processing_charge: No
author:
- first_name: Trevor A
  full_name: Brown, Trevor A
  id: 3569F0A0-F248-11E8-B48F-1D18A9856A87
  last_name: Brown
- first_name: William
  full_name: Sigouin, William
  last_name: Sigouin
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
citation:
  ama: 'Brown TA, Sigouin W, Alistarh D-A. PathCAS: An efficient middle ground for
    concurrent search data structures. In: <i>Proceedings of the 27th ACM SIGPLAN
    Symposium on Principles and Practice of Parallel Programming</i>. Association
    for Computing Machinery; 2022:385-399. doi:<a href="https://doi.org/10.1145/3503221.3508410">10.1145/3503221.3508410</a>'
  apa: 'Brown, T. A., Sigouin, W., &#38; Alistarh, D.-A. (2022). PathCAS: An efficient
    middle ground for concurrent search data structures. In <i>Proceedings of the
    27th ACM SIGPLAN Symposium on Principles and Practice of Parallel Programming</i>
    (pp. 385–399). Seoul, Republic of Korea: Association for Computing Machinery.
    <a href="https://doi.org/10.1145/3503221.3508410">https://doi.org/10.1145/3503221.3508410</a>'
  chicago: 'Brown, Trevor A, William Sigouin, and Dan-Adrian Alistarh. “PathCAS: An
    Efficient Middle Ground for Concurrent Search Data Structures.” In <i>Proceedings
    of the 27th ACM SIGPLAN Symposium on Principles and Practice of Parallel Programming</i>,
    385–99. Association for Computing Machinery, 2022. <a href="https://doi.org/10.1145/3503221.3508410">https://doi.org/10.1145/3503221.3508410</a>.'
  ieee: 'T. A. Brown, W. Sigouin, and D.-A. Alistarh, “PathCAS: An efficient middle
    ground for concurrent search data structures,” in <i>Proceedings of the 27th ACM
    SIGPLAN Symposium on Principles and Practice of Parallel Programming</i>, Seoul,
    Republic of Korea, 2022, pp. 385–399.'
  ista: 'Brown TA, Sigouin W, Alistarh D-A. 2022. PathCAS: An efficient middle ground
    for concurrent search data structures. Proceedings of the 27th ACM SIGPLAN Symposium
    on Principles and Practice of Parallel Programming. PPoPP: Sympopsium on Principles
    and Practice of Parallel Programming, 385–399.'
  mla: 'Brown, Trevor A., et al. “PathCAS: An Efficient Middle Ground for Concurrent
    Search Data Structures.” <i>Proceedings of the 27th ACM SIGPLAN Symposium on Principles
    and Practice of Parallel Programming</i>, Association for Computing Machinery,
    2022, pp. 385–99, doi:<a href="https://doi.org/10.1145/3503221.3508410">10.1145/3503221.3508410</a>.'
  short: T.A. Brown, W. Sigouin, D.-A. Alistarh, in:, Proceedings of the 27th ACM
    SIGPLAN Symposium on Principles and Practice of Parallel Programming, Association
    for Computing Machinery, 2022, pp. 385–399.
conference:
  end_date: 2022-04-06
  location: Seoul, Republic of Korea
  name: 'PPoPP: Sympopsium on Principles and Practice of Parallel Programming'
  start_date: 2022-04-02
date_created: 2022-04-17T22:01:46Z
date_published: 2022-04-02T00:00:00Z
date_updated: 2023-08-03T06:49:20Z
day: '02'
ddc:
- '000'
department:
- _id: DaAl
doi: 10.1145/3503221.3508410
external_id:
  isi:
  - '000883318200027'
file:
- access_level: open_access
  checksum: 8ceea411fa133795cd4903529498eb6b
  content_type: application/pdf
  creator: dernst
  date_created: 2022-08-05T09:19:29Z
  date_updated: 2022-08-05T09:19:29Z
  file_id: '11731'
  file_name: 2022_PPoPP_Brown.pdf
  file_size: 1128343
  relation: main_file
  success: 1
file_date_updated: 2022-08-05T09:19:29Z
has_accepted_license: '1'
isi: 1
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 385-399
publication: Proceedings of the 27th ACM SIGPLAN Symposium on Principles and Practice
  of Parallel Programming
publication_identifier:
  isbn:
  - '9781450392044'
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'PathCAS: An efficient middle ground for concurrent search data structures'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: conference
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
year: '2022'
...
---
_id: '11182'
abstract:
- lang: eng
  text: Immune cells are constantly on the move through multicellular organisms to
    explore and respond to pathogens and other harmful insults. While moving, immune
    cells efficiently traverse microenvironments composed of tissue cells and extracellular
    fibers, which together form complex environments of various porosity, stiffness,
    topography, and chemical composition. In this protocol we describe experimental
    procedures to investigate immune cell migration through microenvironments of heterogeneous
    porosity. In particular, we describe micro-channels, micro-pillars, and collagen
    networks as cell migration paths with alternative pore size choices. Employing
    micro-channels or micro-pillars that divide at junctions into alternative paths
    with initially differentially sized pores allows us to precisely (1) measure the
    cellular translocation time through these porous path junctions, (2) quantify
    the cellular preference for individual pore sizes, and (3) image cellular components
    like the nucleus and the cytoskeleton. This reductionistic experimental setup
    thus can elucidate how immune cells perform decisions in complex microenvironments
    of various porosity like the interstitium. The setup further allows investigation
    of the underlying forces of cellular squeezing and the consequences of cellular
    deformation on the integrity of the cell and its organelles. As a complementary
    approach that does not require any micro-engineering expertise, we describe the
    usage of three-dimensional collagen networks with different pore sizes. Whereas
    we here focus on dendritic cells as a model for motile immune cells, the described
    protocols are versatile as they are also applicable for other immune cell types
    like neutrophils and non-immune cell types such as mesenchymal and cancer cells.
    In summary, we here describe protocols to identify the mechanisms and principles
    of cellular probing, decision making, and squeezing during cellular movement through
    microenvironments of heterogeneous porosity.
acknowledgement: "We thank Kasia Stefanowski for excellent technical assistance, and
  the Core Facility Bioimaging of the Biomedical Center (BMC) of the Ludwig-Maximilian
  University for excellent support. We gratefully acknowledge financial support from
  the Peter Hans Hofschneider Professorship of the Stiftung Experimentelle Biomedizin
  (to J.R), from the DFG (Collaborative Research Center SFB914, project A12; and Priority
  Programme SPP2332, project 492014049; both to J.R) and from the LMU Institutional
  Strategy LMU-Excellent within the framework of the German Excellence Initiative
  (to J.R).\r\nOpen access funding enabled and organized by Projekt DEAL."
article_number: e407
article_processing_charge: No
article_type: original
author:
- first_name: Janina
  full_name: Kroll, Janina
  last_name: Kroll
- first_name: Mauricio J.A.
  full_name: Ruiz-Fernandez, Mauricio J.A.
  last_name: Ruiz-Fernandez
- first_name: Malte B.
  full_name: Braun, Malte B.
  last_name: Braun
- first_name: Jack
  full_name: Merrin, Jack
  id: 4515C308-F248-11E8-B48F-1D18A9856A87
  last_name: Merrin
  orcid: 0000-0001-5145-4609
- first_name: Jörg
  full_name: Renkawitz, Jörg
  id: 3F0587C8-F248-11E8-B48F-1D18A9856A87
  last_name: Renkawitz
  orcid: 0000-0003-2856-3369
citation:
  ama: Kroll J, Ruiz-Fernandez MJA, Braun MB, Merrin J, Renkawitz J. Quantifying the
    probing and selection of microenvironmental pores by motile immune cells. <i>Current
    Protocols</i>. 2022;2(4). doi:<a href="https://doi.org/10.1002/cpz1.407">10.1002/cpz1.407</a>
  apa: Kroll, J., Ruiz-Fernandez, M. J. A., Braun, M. B., Merrin, J., &#38; Renkawitz,
    J. (2022). Quantifying the probing and selection of microenvironmental pores by
    motile immune cells. <i>Current Protocols</i>. Wiley. <a href="https://doi.org/10.1002/cpz1.407">https://doi.org/10.1002/cpz1.407</a>
  chicago: Kroll, Janina, Mauricio J.A. Ruiz-Fernandez, Malte B. Braun, Jack Merrin,
    and Jörg Renkawitz. “Quantifying the Probing and Selection of Microenvironmental
    Pores by Motile Immune Cells.” <i>Current Protocols</i>. Wiley, 2022. <a href="https://doi.org/10.1002/cpz1.407">https://doi.org/10.1002/cpz1.407</a>.
  ieee: J. Kroll, M. J. A. Ruiz-Fernandez, M. B. Braun, J. Merrin, and J. Renkawitz,
    “Quantifying the probing and selection of microenvironmental pores by motile immune
    cells,” <i>Current Protocols</i>, vol. 2, no. 4. Wiley, 2022.
  ista: Kroll J, Ruiz-Fernandez MJA, Braun MB, Merrin J, Renkawitz J. 2022. Quantifying
    the probing and selection of microenvironmental pores by motile immune cells.
    Current Protocols. 2(4), e407.
  mla: Kroll, Janina, et al. “Quantifying the Probing and Selection of Microenvironmental
    Pores by Motile Immune Cells.” <i>Current Protocols</i>, vol. 2, no. 4, e407,
    Wiley, 2022, doi:<a href="https://doi.org/10.1002/cpz1.407">10.1002/cpz1.407</a>.
  short: J. Kroll, M.J.A. Ruiz-Fernandez, M.B. Braun, J. Merrin, J. Renkawitz, Current
    Protocols 2 (2022).
date_created: 2022-04-17T22:01:46Z
date_published: 2022-04-05T00:00:00Z
date_updated: 2022-05-02T08:18:00Z
day: '05'
ddc:
- '570'
department:
- _id: NanoFab
doi: 10.1002/cpz1.407
external_id:
  pmid:
  - '35384410'
file:
- access_level: open_access
  checksum: 72152d005c367777f6cf2f6a477f0d52
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  creator: dernst
  date_created: 2022-05-02T08:16:10Z
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  file_id: '11347'
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  file_size: 2142703
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oa: 1
oa_version: Published Version
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publication: Current Protocols
publication_identifier:
  eissn:
  - 2691-1299
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Quantifying the probing and selection of microenvironmental pores by motile
  immune cells
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2
year: '2022'
...
---
_id: '11183'
abstract:
- lang: eng
  text: "Subgraph detection has recently been one of the most studied problems in
    the CONGEST model of distributed computing. In this work, we study the distributed
    complexity of problems closely related to subgraph detection, mainly focusing
    on induced subgraph detection. The main line of this work presents lower bounds
    and parameterized algorithms w.r.t structural parameters of the input graph:\r\n-
    On general graphs, we give unconditional lower bounds for induced detection of
    cycles and patterns of treewidth 2 in CONGEST. Moreover, by adapting reductions
    from centralized parameterized complexity, we prove lower bounds in CONGEST for
    detecting patterns with a 4-clique, and for induced path detection conditional
    on the hardness of triangle detection in the congested clique.\r\n- On graphs
    of bounded degeneracy, we show that induced paths can be detected fast in CONGEST
    using techniques from parameterized algorithms, while detecting cycles and patterns
    of treewidth 2 is hard.\r\n- On graphs of bounded vertex cover number, we show
    that induced subgraph detection is easy in CONGEST for any pattern graph. More
    specifically, we adapt a centralized parameterized algorithm for a more general
    maximum common induced subgraph detection problem to the distributed setting.
    In addition to these induced subgraph detection results, we study various related
    problems in the CONGEST and congested clique models, including for multicolored
    versions of subgraph-detection-like problems."
acknowledgement: "Amir Nikabadi: Supported by the LABEX MILYON (ANR-10-LABX-0070)
  of Université de Lyon, within the program “Investissements d’Avenir” (ANR-11-IDEX-0007)
  operated by the French National Research Agency (ANR). Janne H. Korhonen: Supported
  by the European Research Council (ERC) under the European Union’s Horizon 2020 research
  and innovation programme (grant agreement No 805223 ScaleML).\r\nWe thank François
  Le Gall and Masayuki Miyamoto for sharing their work on lower bounds for induced
  subgraph detection [36]."
alternative_title:
- LIPIcs
article_number: '15'
article_processing_charge: No
author:
- first_name: Amir
  full_name: Nikabadi, Amir
  last_name: Nikabadi
- first_name: Janne
  full_name: Korhonen, Janne
  id: C5402D42-15BC-11E9-A202-CA2BE6697425
  last_name: Korhonen
citation:
  ama: 'Nikabadi A, Korhonen J. Beyond distributed subgraph detection: Induced subgraphs,
    multicolored problems and graph parameters. In: Bramas Q, Gramoli V, Milani A,
    eds. <i>25th International Conference on Principles of Distributed Systems</i>.
    Vol 217. Schloss Dagstuhl - Leibniz-Zentrum für Informatik; 2022. doi:<a href="https://doi.org/10.4230/LIPIcs.OPODIS.2021.15">10.4230/LIPIcs.OPODIS.2021.15</a>'
  apa: 'Nikabadi, A., &#38; Korhonen, J. (2022). Beyond distributed subgraph detection:
    Induced subgraphs, multicolored problems and graph parameters. In Q. Bramas, V.
    Gramoli, &#38; A. Milani (Eds.), <i>25th International Conference on Principles
    of Distributed Systems</i> (Vol. 217). Strasbourg, France: Schloss Dagstuhl -
    Leibniz-Zentrum für Informatik. <a href="https://doi.org/10.4230/LIPIcs.OPODIS.2021.15">https://doi.org/10.4230/LIPIcs.OPODIS.2021.15</a>'
  chicago: 'Nikabadi, Amir, and Janne Korhonen. “Beyond Distributed Subgraph Detection:
    Induced Subgraphs, Multicolored Problems and Graph Parameters.” In <i>25th International
    Conference on Principles of Distributed Systems</i>, edited by Quentin Bramas,
    Vincent Gramoli, and Alessia Milani, Vol. 217. Schloss Dagstuhl - Leibniz-Zentrum
    für Informatik, 2022. <a href="https://doi.org/10.4230/LIPIcs.OPODIS.2021.15">https://doi.org/10.4230/LIPIcs.OPODIS.2021.15</a>.'
  ieee: 'A. Nikabadi and J. Korhonen, “Beyond distributed subgraph detection: Induced
    subgraphs, multicolored problems and graph parameters,” in <i>25th International
    Conference on Principles of Distributed Systems</i>, Strasbourg, France, 2022,
    vol. 217.'
  ista: 'Nikabadi A, Korhonen J. 2022. Beyond distributed subgraph detection: Induced
    subgraphs, multicolored problems and graph parameters. 25th International Conference
    on Principles of Distributed Systems. OPODIS, LIPIcs, vol. 217, 15.'
  mla: 'Nikabadi, Amir, and Janne Korhonen. “Beyond Distributed Subgraph Detection:
    Induced Subgraphs, Multicolored Problems and Graph Parameters.” <i>25th International
    Conference on Principles of Distributed Systems</i>, edited by Quentin Bramas
    et al., vol. 217, 15, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2022,
    doi:<a href="https://doi.org/10.4230/LIPIcs.OPODIS.2021.15">10.4230/LIPIcs.OPODIS.2021.15</a>.'
  short: A. Nikabadi, J. Korhonen, in:, Q. Bramas, V. Gramoli, A. Milani (Eds.), 25th
    International Conference on Principles of Distributed Systems, Schloss Dagstuhl
    - Leibniz-Zentrum für Informatik, 2022.
conference:
  end_date: 2021-12-15
  location: Strasbourg, France
  name: OPODIS
  start_date: 2021-12-13
date_created: 2022-04-17T22:01:47Z
date_published: 2022-02-01T00:00:00Z
date_updated: 2022-05-02T07:56:35Z
day: '01'
ddc:
- '510'
department:
- _id: DaAl
doi: 10.4230/LIPIcs.OPODIS.2021.15
ec_funded: 1
editor:
- first_name: Quentin
  full_name: Bramas, Quentin
  last_name: Bramas
- first_name: Vincent
  full_name: Gramoli, Vincent
  last_name: Gramoli
- first_name: Alessia
  full_name: Milani, Alessia
  last_name: Milani
file:
- access_level: open_access
  checksum: 626551c14de5d4091573200ed0535752
  content_type: application/pdf
  creator: dernst
  date_created: 2022-05-02T07:53:00Z
  date_updated: 2022-05-02T07:53:00Z
  file_id: '11345'
  file_name: 2022_LIPICs_Nikabadi.pdf
  file_size: 790396
  relation: main_file
  success: 1
file_date_updated: 2022-05-02T07:53:00Z
has_accepted_license: '1'
intvolume: '       217'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
project:
- _id: 268A44D6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '805223'
  name: Elastic Coordination for Scalable Machine Learning
publication: 25th International Conference on Principles of Distributed Systems
publication_identifier:
  isbn:
  - '9783959772198'
  issn:
  - 1868-8969
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Beyond distributed subgraph detection: Induced subgraphs, multicolored problems
  and graph parameters'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 217
year: '2022'
...
