---
_id: '279'
abstract:
- lang: eng
  text: 'Background: Natural selection shapes cancer genomes. Previous studies used
    signatures of positive selection to identify genes driving malignant transformation.
    However, the contribution of negative selection against somatic mutations that
    affect essential tumor functions or specific domains remains a controversial topic.
    Results: Here, we analyze 7546 individual exomes from 26 tumor types from TCGA
    data to explore the portion of the cancer exome under negative selection. Although
    we find most of the genes neutrally evolving in a pan-cancer framework, we identify
    essential cancer genes and immune-exposed protein regions under significant negative
    selection. Moreover, our simulations suggest that the amount of negative selection
    is underestimated. We therefore choose an empirical approach to identify genes,
    functions, and protein regions under negative selection. We find that expression
    and mutation status of negatively selected genes is indicative of patient survival.
    Processes that are most strongly conserved are those that play fundamental cellular
    roles such as protein synthesis, glucose metabolism, and molecular transport.
    Intriguingly, we observe strong signals of selection in the immunopeptidome and
    proteins controlling peptide exposition, highlighting the importance of immune
    surveillance evasion. Additionally, tumor type-specific immune activity correlates
    with the strength of negative selection on human epitopes. Conclusions: In summary,
    our results show that negative selection is a hallmark of cell essentiality and
    immune response in cancer. The functional domains identified could be exploited
    therapeutically, ultimately allowing for the development of novel cancer treatments.'
article_number: '67'
article_processing_charge: No
author:
- first_name: Luis
  full_name: Zapata, Luis
  last_name: Zapata
- first_name: Oriol
  full_name: Pich, Oriol
  last_name: Pich
- first_name: Luis
  full_name: Serrano, Luis
  last_name: Serrano
- first_name: Fyodor
  full_name: Kondrashov, Fyodor
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
- first_name: Stephan
  full_name: Ossowski, Stephan
  last_name: Ossowski
- first_name: Martin
  full_name: Schaefer, Martin
  last_name: Schaefer
citation:
  ama: Zapata L, Pich O, Serrano L, Kondrashov F, Ossowski S, Schaefer M. Negative
    selection in tumor genome evolution acts on essential cellular functions and the
    immunopeptidome. <i>Genome Biology</i>. 2018;19. doi:<a href="https://doi.org/10.1186/s13059-018-1434-0">10.1186/s13059-018-1434-0</a>
  apa: Zapata, L., Pich, O., Serrano, L., Kondrashov, F., Ossowski, S., &#38; Schaefer,
    M. (2018). Negative selection in tumor genome evolution acts on essential cellular
    functions and the immunopeptidome. <i>Genome Biology</i>. BioMed Central. <a href="https://doi.org/10.1186/s13059-018-1434-0">https://doi.org/10.1186/s13059-018-1434-0</a>
  chicago: Zapata, Luis, Oriol Pich, Luis Serrano, Fyodor Kondrashov, Stephan Ossowski,
    and Martin Schaefer. “Negative Selection in Tumor Genome Evolution Acts on Essential
    Cellular Functions and the Immunopeptidome.” <i>Genome Biology</i>. BioMed Central,
    2018. <a href="https://doi.org/10.1186/s13059-018-1434-0">https://doi.org/10.1186/s13059-018-1434-0</a>.
  ieee: L. Zapata, O. Pich, L. Serrano, F. Kondrashov, S. Ossowski, and M. Schaefer,
    “Negative selection in tumor genome evolution acts on essential cellular functions
    and the immunopeptidome,” <i>Genome Biology</i>, vol. 19. BioMed Central, 2018.
  ista: Zapata L, Pich O, Serrano L, Kondrashov F, Ossowski S, Schaefer M. 2018. Negative
    selection in tumor genome evolution acts on essential cellular functions and the
    immunopeptidome. Genome Biology. 19, 67.
  mla: Zapata, Luis, et al. “Negative Selection in Tumor Genome Evolution Acts on
    Essential Cellular Functions and the Immunopeptidome.” <i>Genome Biology</i>,
    vol. 19, 67, BioMed Central, 2018, doi:<a href="https://doi.org/10.1186/s13059-018-1434-0">10.1186/s13059-018-1434-0</a>.
  short: L. Zapata, O. Pich, L. Serrano, F. Kondrashov, S. Ossowski, M. Schaefer,
    Genome Biology 19 (2018).
date_created: 2018-12-11T11:45:35Z
date_published: 2018-05-31T00:00:00Z
date_updated: 2023-09-13T09:01:32Z
day: '31'
ddc:
- '570'
department:
- _id: FyKo
doi: 10.1186/s13059-018-1434-0
ec_funded: 1
external_id:
  isi:
  - '000433986200001'
file:
- access_level: open_access
  checksum: f3e4922486bd9bf1483271bdbed394a7
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T14:05:01Z
  date_updated: 2020-07-14T12:45:47Z
  file_id: '5708'
  file_name: 2018_GenomeBiology_Zapata.pdf
  file_size: 1414722
  relation: main_file
file_date_updated: 2020-07-14T12:45:47Z
has_accepted_license: '1'
intvolume: '        19'
isi: 1
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
project:
- _id: 26120F5C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '335980'
  name: Systematic investigation of epistasis in molecular evolution
publication: Genome Biology
publication_status: published
publisher: BioMed Central
publist_id: '7620'
quality_controlled: '1'
related_material:
  record:
  - id: '9811'
    relation: research_data
    status: public
  - id: '9812'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Negative selection in tumor genome evolution acts on essential cellular functions
  and the immunopeptidome
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 19
year: '2018'
...
---
_id: '28'
abstract:
- lang: eng
  text: 'This scientific commentary refers to ‘NEGR1 and FGFR2 cooperatively regulate
    cortical development and core behaviours related to autism disorders in mice’
    by Szczurkowska et al. '
article_processing_charge: No
author:
- first_name: Ximena
  full_name: Contreras, Ximena
  id: 475990FE-F248-11E8-B48F-1D18A9856A87
  last_name: Contreras
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
citation:
  ama: Contreras X, Hippenmeyer S. Incorrect trafficking route leads to autism. <i>Brain
    a journal of neurology</i>. 2018;141(9):2542-2544. doi:<a href="https://doi.org/10.1093/brain/awy218">10.1093/brain/awy218</a>
  apa: Contreras, X., &#38; Hippenmeyer, S. (2018). Incorrect trafficking route leads
    to autism. <i>Brain a Journal of Neurology</i>. Oxford University Press. <a href="https://doi.org/10.1093/brain/awy218">https://doi.org/10.1093/brain/awy218</a>
  chicago: Contreras, Ximena, and Simon Hippenmeyer. “Incorrect Trafficking Route
    Leads to Autism.” <i>Brain a Journal of Neurology</i>. Oxford University Press,
    2018. <a href="https://doi.org/10.1093/brain/awy218">https://doi.org/10.1093/brain/awy218</a>.
  ieee: X. Contreras and S. Hippenmeyer, “Incorrect trafficking route leads to autism,”
    <i>Brain a journal of neurology</i>, vol. 141, no. 9. Oxford University Press,
    pp. 2542–2544, 2018.
  ista: Contreras X, Hippenmeyer S. 2018. Incorrect trafficking route leads to autism.
    Brain a journal of neurology. 141(9), 2542–2544.
  mla: Contreras, Ximena, and Simon Hippenmeyer. “Incorrect Trafficking Route Leads
    to Autism.” <i>Brain a Journal of Neurology</i>, vol. 141, no. 9, Oxford University
    Press, 2018, pp. 2542–44, doi:<a href="https://doi.org/10.1093/brain/awy218">10.1093/brain/awy218</a>.
  short: X. Contreras, S. Hippenmeyer, Brain a Journal of Neurology 141 (2018) 2542–2544.
date_created: 2018-12-11T11:44:14Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2024-03-25T23:30:23Z
day: '01'
department:
- _id: SiHi
doi: 10.1093/brain/awy218
external_id:
  isi:
  - '000446548100012'
intvolume: '       141'
isi: 1
issue: '9'
language:
- iso: eng
month: '09'
oa_version: None
page: 2542 - 2544
publication: Brain a journal of neurology
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
related_material:
  record:
  - id: '7902'
    relation: part_of_dissertation
    status: public
scopus_import: '1'
status: public
title: Incorrect trafficking route leads to autism
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 141
year: '2018'
...
---
_id: '280'
abstract:
- lang: eng
  text: Flowers have a species-specific functional life span that determines the time
    window in which pollination, fertilization and seed set can occur. The stigma
    tissue plays a key role in flower receptivity by intercepting pollen and initiating
    pollen tube growth toward the ovary. In this article, we show that a developmentally
    controlled cell death programme terminates the functional life span of stigma
    cells in Arabidopsis. We identified the leaf senescence regulator ORESARA1 (also
    known as ANAC092) and the previously uncharacterized KIRA1 (also known as ANAC074)
    as partially redundant transcription factors that modulate stigma longevity by
    controlling the expression of programmed cell death-associated genes. KIRA1 expression
    is sufficient to induce cell death and terminate floral receptivity, whereas lack
    of both KIRA1 and ORESARA1 substantially increases stigma life span. Surprisingly,
    the extension of stigma longevity is accompanied by only a moderate extension
    of flower receptivity, suggesting that additional processes participate in the
    control of the flower's receptive life span.
acknowledgement: We gratefully acknowledge funding from the Chinese Scholarship Council
  (CSC; project number 201206910025 to Z.G.), the Fonds Wetenschappelijk Onderzoek
  (FWO; project number G005112N to A.D.; fellowship number 12I7417N to Z.L.), the
  Belgian Federal Science Policy Office (BELSPO; to Y.S.), the Agency for Innovation
  by Science and Technology of Belgium (IWT; fellowship number 121110 to M.V.D.),
  the Hercules foundation (grant AUGE-09-029 to K.D.), and the ERC StG PROCELLDEATH
  (project number 639234 to M.K.N.).
article_processing_charge: No
author:
- first_name: Zhen
  full_name: Gao, Zhen
  last_name: Gao
- first_name: Anna
  full_name: Daneva, Anna
  last_name: Daneva
- first_name: Yuliya
  full_name: Salanenka, Yuliya
  id: 46DAAE7E-F248-11E8-B48F-1D18A9856A87
  last_name: Salanenka
- first_name: Matthias
  full_name: Van Durme, Matthias
  last_name: Van Durme
- first_name: Marlies
  full_name: Huysmans, Marlies
  last_name: Huysmans
- first_name: Zongcheng
  full_name: Lin, Zongcheng
  last_name: Lin
- first_name: Freya
  full_name: De Winter, Freya
  last_name: De Winter
- first_name: Steffen
  full_name: Vanneste, Steffen
  last_name: Vanneste
- first_name: Mansour
  full_name: Karimi, Mansour
  last_name: Karimi
- first_name: Jan
  full_name: Van De Velde, Jan
  last_name: Van De Velde
- first_name: Klaas
  full_name: Vandepoele, Klaas
  last_name: Vandepoele
- first_name: Davy
  full_name: Van De Walle, Davy
  last_name: Van De Walle
- first_name: Koen
  full_name: Dewettinck, Koen
  last_name: Dewettinck
- first_name: Bart
  full_name: Lambrecht, Bart
  last_name: Lambrecht
- first_name: Moritz
  full_name: Nowack, Moritz
  last_name: Nowack
citation:
  ama: Gao Z, Daneva A, Salanenka Y, et al. KIRA1 and ORESARA1 terminate flower receptivity
    by promoting cell death in the stigma of Arabidopsis. <i>Nature Plants</i>. 2018;4(6):365-375.
    doi:<a href="https://doi.org/10.1038/s41477-018-0160-7">10.1038/s41477-018-0160-7</a>
  apa: Gao, Z., Daneva, A., Salanenka, Y., Van Durme, M., Huysmans, M., Lin, Z., …
    Nowack, M. (2018). KIRA1 and ORESARA1 terminate flower receptivity by promoting
    cell death in the stigma of Arabidopsis. <i>Nature Plants</i>. Nature Publishing
    Group. <a href="https://doi.org/10.1038/s41477-018-0160-7">https://doi.org/10.1038/s41477-018-0160-7</a>
  chicago: Gao, Zhen, Anna Daneva, Yuliya Salanenka, Matthias Van Durme, Marlies Huysmans,
    Zongcheng Lin, Freya De Winter, et al. “KIRA1 and ORESARA1 Terminate Flower Receptivity
    by Promoting Cell Death in the Stigma of Arabidopsis.” <i>Nature Plants</i>. Nature
    Publishing Group, 2018. <a href="https://doi.org/10.1038/s41477-018-0160-7">https://doi.org/10.1038/s41477-018-0160-7</a>.
  ieee: Z. Gao <i>et al.</i>, “KIRA1 and ORESARA1 terminate flower receptivity by
    promoting cell death in the stigma of Arabidopsis,” <i>Nature Plants</i>, vol.
    4, no. 6. Nature Publishing Group, pp. 365–375, 2018.
  ista: Gao Z, Daneva A, Salanenka Y, Van Durme M, Huysmans M, Lin Z, De Winter F,
    Vanneste S, Karimi M, Van De Velde J, Vandepoele K, Van De Walle D, Dewettinck
    K, Lambrecht B, Nowack M. 2018. KIRA1 and ORESARA1 terminate flower receptivity
    by promoting cell death in the stigma of Arabidopsis. Nature Plants. 4(6), 365–375.
  mla: Gao, Zhen, et al. “KIRA1 and ORESARA1 Terminate Flower Receptivity by Promoting
    Cell Death in the Stigma of Arabidopsis.” <i>Nature Plants</i>, vol. 4, no. 6,
    Nature Publishing Group, 2018, pp. 365–75, doi:<a href="https://doi.org/10.1038/s41477-018-0160-7">10.1038/s41477-018-0160-7</a>.
  short: Z. Gao, A. Daneva, Y. Salanenka, M. Van Durme, M. Huysmans, Z. Lin, F. De
    Winter, S. Vanneste, M. Karimi, J. Van De Velde, K. Vandepoele, D. Van De Walle,
    K. Dewettinck, B. Lambrecht, M. Nowack, Nature Plants 4 (2018) 365–375.
date_created: 2018-12-11T11:45:35Z
date_published: 2018-05-28T00:00:00Z
date_updated: 2023-09-13T08:24:17Z
day: '28'
department:
- _id: JiFr
doi: 10.1038/s41477-018-0160-7
external_id:
  isi:
  - '000435571000017'
intvolume: '         4'
isi: 1
issue: '6'
language:
- iso: eng
month: '05'
oa_version: None
page: 365 - 375
publication: Nature Plants
publication_status: published
publisher: Nature Publishing Group
publist_id: '7619'
quality_controlled: '1'
scopus_import: '1'
status: public
title: KIRA1 and ORESARA1 terminate flower receptivity by promoting cell death in
  the stigma of Arabidopsis
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 4
year: '2018'
...
---
_id: '281'
abstract:
- lang: eng
  text: 'Although cells respond specifically to environments, how environmental identity
    is encoded intracellularly is not understood. Here, we study this organization
    of information in budding yeast by estimating the mutual information between environmental
    transitions and the dynamics of nuclear translocation for 10 transcription factors.
    Our method of estimation is general, scalable, and based on decoding from single
    cells. The dynamics of the transcription factors are necessary to encode the highest
    amounts of extracellular information, and we show that information is transduced
    through two channels: Generalists (Msn2/4, Tod6 and Dot6, Maf1, and Sfp1) can
    encode the nature of multiple stresses, but only if stress is high; specialists
    (Hog1, Yap1, and Mig1/2) encode one particular stress, but do so more quickly
    and for a wider range of magnitudes. In particular, Dot6 encodes almost as much
    information as Msn2, the master regulator of the environmental stress response.
    Each transcription factor reports differently, and it is only their collective
    behavior that distinguishes between multiple environmental states. Changes in
    the dynamics of the localization of transcription factors thus constitute a precise,
    distributed internal representation of extracellular change. We predict that such
    multidimensional representations are common in cellular decision-making.'
acknowledgement: This work was supported by the Biotechnology and Biological Sciences
  Research Council (J.M.J.P., I.F., and P.S.S.), the Engineering and Physical Sciences
  Research Council (EPSRC) (A.A.G.), and Austrian Science Fund Grant FWF P28844 (to
  G.T.).
article_processing_charge: No
article_type: original
author:
- first_name: Alejandro
  full_name: Granados, Alejandro
  last_name: Granados
- first_name: Julian
  full_name: Pietsch, Julian
  last_name: Pietsch
- first_name: Sarah A
  full_name: Cepeda Humerez, Sarah A
  id: 3DEE19A4-F248-11E8-B48F-1D18A9856A87
  last_name: Cepeda Humerez
- first_name: Isebail
  full_name: Farquhar, Isebail
  last_name: Farquhar
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
- first_name: Peter
  full_name: Swain, Peter
  last_name: Swain
citation:
  ama: Granados A, Pietsch J, Cepeda Humerez SA, Farquhar I, Tkačik G, Swain P. Distributed
    and dynamic intracellular organization of extracellular information. <i>PNAS</i>.
    2018;115(23):6088-6093. doi:<a href="https://doi.org/10.1073/pnas.1716659115">10.1073/pnas.1716659115</a>
  apa: Granados, A., Pietsch, J., Cepeda Humerez, S. A., Farquhar, I., Tkačik, G.,
    &#38; Swain, P. (2018). Distributed and dynamic intracellular organization of
    extracellular information. <i>PNAS</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1716659115">https://doi.org/10.1073/pnas.1716659115</a>
  chicago: Granados, Alejandro, Julian Pietsch, Sarah A Cepeda Humerez, Isebail Farquhar,
    Gašper Tkačik, and Peter Swain. “Distributed and Dynamic Intracellular Organization
    of Extracellular Information.” <i>PNAS</i>. National Academy of Sciences, 2018.
    <a href="https://doi.org/10.1073/pnas.1716659115">https://doi.org/10.1073/pnas.1716659115</a>.
  ieee: A. Granados, J. Pietsch, S. A. Cepeda Humerez, I. Farquhar, G. Tkačik, and
    P. Swain, “Distributed and dynamic intracellular organization of extracellular
    information,” <i>PNAS</i>, vol. 115, no. 23. National Academy of Sciences, pp.
    6088–6093, 2018.
  ista: Granados A, Pietsch J, Cepeda Humerez SA, Farquhar I, Tkačik G, Swain P. 2018.
    Distributed and dynamic intracellular organization of extracellular information.
    PNAS. 115(23), 6088–6093.
  mla: Granados, Alejandro, et al. “Distributed and Dynamic Intracellular Organization
    of Extracellular Information.” <i>PNAS</i>, vol. 115, no. 23, National Academy
    of Sciences, 2018, pp. 6088–93, doi:<a href="https://doi.org/10.1073/pnas.1716659115">10.1073/pnas.1716659115</a>.
  short: A. Granados, J. Pietsch, S.A. Cepeda Humerez, I. Farquhar, G. Tkačik, P.
    Swain, PNAS 115 (2018) 6088–6093.
date_created: 2018-12-11T11:45:35Z
date_published: 2018-06-05T00:00:00Z
date_updated: 2023-09-11T12:58:24Z
day: '05'
department:
- _id: GaTk
doi: 10.1073/pnas.1716659115
external_id:
  isi:
  - '000434114900071'
  pmid:
  - '29784812'
intvolume: '       115'
isi: 1
issue: '23'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.biorxiv.org/content/early/2017/09/21/192039
month: '06'
oa: 1
oa_version: Preprint
page: 6088 - 6093
pmid: 1
project:
- _id: 254E9036-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P28844-B27
  name: Biophysics of information processing in gene regulation
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '7618'
quality_controlled: '1'
related_material:
  record:
  - id: '6473'
    relation: part_of_dissertation
    status: public
scopus_import: '1'
status: public
title: Distributed and dynamic intracellular organization of extracellular information
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 115
year: '2018'
...
---
_id: '282'
abstract:
- lang: eng
  text: Adaptive introgression is common in nature and can be driven by selection
    acting on multiple, linked genes. We explore the effects of polygenic selection
    on introgression under the infinitesimal model with linkage. This model assumes
    that the introgressing block has an effectively infinite number of genes, each
    with an infinitesimal effect on the trait under selection. The block is assumed
    to introgress under directional selection within a native population that is genetically
    homogeneous. We use individual-based simulations and a branching process approximation
    to compute various statistics of the introgressing block, and explore how these
    depend on parameters such as the map length and initial trait value associated
    with the introgressing block, the genetic variability along the block, and the
    strength of selection. Our results show that the introgression dynamics of a block
    under infinitesimal selection is qualitatively different from the dynamics of
    neutral introgression. We also find that in the long run, surviving descendant
    blocks are likely to have intermediate lengths, and clarify how the length is
    shaped by the interplay between linkage and infinitesimal selection. Our results
    suggest that it may be difficult to distinguish introgression of single loci from
    that of genomic blocks with multiple, tightly linked and weakly selected loci.
article_processing_charge: No
author:
- first_name: Himani
  full_name: Sachdeva, Himani
  id: 42377A0A-F248-11E8-B48F-1D18A9856A87
  last_name: Sachdeva
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: Sachdeva H, Barton NH. Introgression of a block of genome under infinitesimal
    selection. <i>Genetics</i>. 2018;209(4):1279-1303. doi:<a href="https://doi.org/10.1534/genetics.118.301018">10.1534/genetics.118.301018</a>
  apa: Sachdeva, H., &#38; Barton, N. H. (2018). Introgression of a block of genome
    under infinitesimal selection. <i>Genetics</i>. Genetics Society of America. <a
    href="https://doi.org/10.1534/genetics.118.301018">https://doi.org/10.1534/genetics.118.301018</a>
  chicago: Sachdeva, Himani, and Nicholas H Barton. “Introgression of a Block of Genome
    under Infinitesimal Selection.” <i>Genetics</i>. Genetics Society of America,
    2018. <a href="https://doi.org/10.1534/genetics.118.301018">https://doi.org/10.1534/genetics.118.301018</a>.
  ieee: H. Sachdeva and N. H. Barton, “Introgression of a block of genome under infinitesimal
    selection,” <i>Genetics</i>, vol. 209, no. 4. Genetics Society of America, pp.
    1279–1303, 2018.
  ista: Sachdeva H, Barton NH. 2018. Introgression of a block of genome under infinitesimal
    selection. Genetics. 209(4), 1279–1303.
  mla: Sachdeva, Himani, and Nicholas H. Barton. “Introgression of a Block of Genome
    under Infinitesimal Selection.” <i>Genetics</i>, vol. 209, no. 4, Genetics Society
    of America, 2018, pp. 1279–303, doi:<a href="https://doi.org/10.1534/genetics.118.301018">10.1534/genetics.118.301018</a>.
  short: H. Sachdeva, N.H. Barton, Genetics 209 (2018) 1279–1303.
date_created: 2018-12-11T11:45:36Z
date_published: 2018-08-01T00:00:00Z
date_updated: 2023-09-13T08:22:32Z
day: '01'
department:
- _id: NiBa
doi: 10.1534/genetics.118.301018
external_id:
  isi:
  - '000440014100020'
intvolume: '       209'
isi: 1
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.biorxiv.org/content/early/2017/11/30/227082
month: '08'
oa: 1
oa_version: Submitted Version
page: 1279 - 1303
publication: Genetics
publication_status: published
publisher: Genetics Society of America
publist_id: '7617'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Introgression of a block of genome under infinitesimal selection
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 209
year: '2018'
...
---
_id: '283'
abstract:
- lang: eng
  text: Light represents the principal signal driving circadian clock entrainment.
    However, how light influences the evolution of the clock remains poorly understood.
    The cavefish Phreatichthys andruzzii represents a fascinating model to explore
    how evolution under extreme aphotic conditions shapes the circadian clock, since
    in this species the clock is unresponsive to light. We have previously demonstrated
    that loss-of-function mutations targeting non-visual opsins contribute in part
    to this blind clock phenotype. Here, we have compared orthologs of two core clock
    genes that play a key role in photic entrainment, cry1a and per2, in both zebrafish
    and P. andruzzii. We encountered aberrantly spliced variants for the P. andruzzii
    per2 transcript. The most abundant transcript encodes a truncated protein lacking
    the C-terminal Cry binding domain and incorporating an intronic, transposon-derived
    coding sequence. We demonstrate that the transposon insertion leads to a predominantly
    cytoplasmic localization of the cavefish Per2 protein in contrast to the zebrafish
    ortholog which is distributed in both the nucleus and cytoplasm. Thus, it seems
    that during evolution in complete darkness, the photic entrainment pathway of
    the circadian clock has been subject to mutation at multiple levels, extending
    from opsin photoreceptors to nuclear effectors.
article_number: '8754'
article_processing_charge: No
author:
- first_name: Rosa Maria
  full_name: Ceinos, Rosa Maria
  last_name: Ceinos
- first_name: Elena
  full_name: Frigato, Elena
  last_name: Frigato
- first_name: Cristina
  full_name: Pagano, Cristina
  last_name: Pagano
- first_name: Nadine
  full_name: Frohlich, Nadine
  last_name: Frohlich
- first_name: Pietro
  full_name: Negrini, Pietro
  last_name: Negrini
- first_name: Nicola
  full_name: Cavallari, Nicola
  id: 457160E6-F248-11E8-B48F-1D18A9856A87
  last_name: Cavallari
- first_name: Daniela
  full_name: Vallone, Daniela
  last_name: Vallone
- first_name: Silvia
  full_name: Fuselli, Silvia
  last_name: Fuselli
- first_name: Cristiano
  full_name: Bertolucci, Cristiano
  last_name: Bertolucci
- first_name: Nicholas S
  full_name: Foulkes, Nicholas S
  last_name: Foulkes
citation:
  ama: Ceinos RM, Frigato E, Pagano C, et al. Mutations in blind cavefish target the
    light regulated circadian clock gene period 2. <i>Scientific Reports</i>. 2018;8(1).
    doi:<a href="https://doi.org/10.1038/s41598-018-27080-2">10.1038/s41598-018-27080-2</a>
  apa: Ceinos, R. M., Frigato, E., Pagano, C., Frohlich, N., Negrini, P., Cavallari,
    N., … Foulkes, N. S. (2018). Mutations in blind cavefish target the light regulated
    circadian clock gene period 2. <i>Scientific Reports</i>. Nature Publishing Group.
    <a href="https://doi.org/10.1038/s41598-018-27080-2">https://doi.org/10.1038/s41598-018-27080-2</a>
  chicago: Ceinos, Rosa Maria, Elena Frigato, Cristina Pagano, Nadine Frohlich, Pietro
    Negrini, Nicola Cavallari, Daniela Vallone, Silvia Fuselli, Cristiano Bertolucci,
    and Nicholas S Foulkes. “Mutations in Blind Cavefish Target the Light Regulated
    Circadian Clock Gene Period 2.” <i>Scientific Reports</i>. Nature Publishing Group,
    2018. <a href="https://doi.org/10.1038/s41598-018-27080-2">https://doi.org/10.1038/s41598-018-27080-2</a>.
  ieee: R. M. Ceinos <i>et al.</i>, “Mutations in blind cavefish target the light
    regulated circadian clock gene period 2,” <i>Scientific Reports</i>, vol. 8, no.
    1. Nature Publishing Group, 2018.
  ista: Ceinos RM, Frigato E, Pagano C, Frohlich N, Negrini P, Cavallari N, Vallone
    D, Fuselli S, Bertolucci C, Foulkes NS. 2018. Mutations in blind cavefish target
    the light regulated circadian clock gene period 2. Scientific Reports. 8(1), 8754.
  mla: Ceinos, Rosa Maria, et al. “Mutations in Blind Cavefish Target the Light Regulated
    Circadian Clock Gene Period 2.” <i>Scientific Reports</i>, vol. 8, no. 1, 8754,
    Nature Publishing Group, 2018, doi:<a href="https://doi.org/10.1038/s41598-018-27080-2">10.1038/s41598-018-27080-2</a>.
  short: R.M. Ceinos, E. Frigato, C. Pagano, N. Frohlich, P. Negrini, N. Cavallari,
    D. Vallone, S. Fuselli, C. Bertolucci, N.S. Foulkes, Scientific Reports 8 (2018).
date_created: 2018-12-11T11:45:36Z
date_published: 2018-06-08T00:00:00Z
date_updated: 2023-09-13T08:59:27Z
day: '08'
ddc:
- '570'
department:
- _id: EvBe
doi: 10.1038/s41598-018-27080-2
external_id:
  isi:
  - '000434640800008'
file:
- access_level: open_access
  checksum: 9c3942d772f84f3df032ffde0ed9a8ea
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T13:04:46Z
  date_updated: 2020-07-14T12:45:49Z
  file_id: '5707'
  file_name: 2018_ScientificReports_Ceinos.pdf
  file_size: 1855324
  relation: main_file
file_date_updated: 2020-07-14T12:45:49Z
has_accepted_license: '1'
intvolume: '         8'
isi: 1
issue: '1'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: Scientific Reports
publication_status: published
publisher: Nature Publishing Group
publist_id: '7616'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mutations in blind cavefish target the light regulated circadian clock gene
  period 2
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 8
year: '2018'
...
---
_id: '284'
abstract:
- lang: eng
  text: "Borel probability measures living on metric spaces are fundamental\r\nmathematical
    objects. There are several meaningful distance functions that make the collection
    of the probability measures living on a certain space a metric space. We are interested
    in the description of the structure of the isometries of such metric spaces. We
    overview some of the recent results of the topic and we also provide some new
    ones concerning the Wasserstein distance. More specifically, we consider the space
    of all Borel probability measures on the unit sphere of a Euclidean space endowed
    with the Wasserstein metric W_p for arbitrary p &gt;= 1, and we show that the
    action of a Wasserstein isometry on the set of Dirac measures is induced by an
    isometry of the underlying unit sphere."
acknowledgement: The author was supported by the ISTFELLOW program of the Institute
  of Science and Technol- ogy Austria (project code IC1027FELL01) and partially supported
  by the Hungarian National Research, Development and Innovation Office, NKFIH (grant
  no. K124152).
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Daniel
  full_name: Virosztek, Daniel
  id: 48DB45DA-F248-11E8-B48F-1D18A9856A87
  last_name: Virosztek
  orcid: 0000-0003-1109-5511
citation:
  ama: Virosztek D. Maps on probability measures preserving certain distances - a
    survey and some new results. <i>Acta Scientiarum Mathematicarum</i>. 2018;84(1-2):65-80.
    doi:<a href="https://doi.org/10.14232/actasm-018-753-y">10.14232/actasm-018-753-y</a>
  apa: Virosztek, D. (2018). Maps on probability measures preserving certain distances
    - a survey and some new results. <i>Acta Scientiarum Mathematicarum</i>. Springer
    Nature. <a href="https://doi.org/10.14232/actasm-018-753-y">https://doi.org/10.14232/actasm-018-753-y</a>
  chicago: Virosztek, Daniel. “Maps on Probability Measures Preserving Certain Distances
    - a Survey and Some New Results.” <i>Acta Scientiarum Mathematicarum</i>. Springer
    Nature, 2018. <a href="https://doi.org/10.14232/actasm-018-753-y">https://doi.org/10.14232/actasm-018-753-y</a>.
  ieee: D. Virosztek, “Maps on probability measures preserving certain distances -
    a survey and some new results,” <i>Acta Scientiarum Mathematicarum</i>, vol. 84,
    no. 1–2. Springer Nature, pp. 65–80, 2018.
  ista: Virosztek D. 2018. Maps on probability measures preserving certain distances
    - a survey and some new results. Acta Scientiarum Mathematicarum. 84(1–2), 65–80.
  mla: Virosztek, Daniel. “Maps on Probability Measures Preserving Certain Distances
    - a Survey and Some New Results.” <i>Acta Scientiarum Mathematicarum</i>, vol.
    84, no. 1–2, Springer Nature, 2018, pp. 65–80, doi:<a href="https://doi.org/10.14232/actasm-018-753-y">10.14232/actasm-018-753-y</a>.
  short: D. Virosztek, Acta Scientiarum Mathematicarum 84 (2018) 65–80.
date_created: 2018-12-11T11:45:36Z
date_published: 2018-06-04T00:00:00Z
date_updated: 2023-10-16T10:29:22Z
day: '04'
department:
- _id: LaEr
doi: 10.14232/actasm-018-753-y
ec_funded: 1
external_id:
  arxiv:
  - '1802.03305'
intvolume: '        84'
issue: 1-2
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1802.03305
month: '06'
oa: 1
oa_version: Preprint
page: 65 - 80
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: Acta Scientiarum Mathematicarum
publication_identifier:
  eissn:
  - 2064-8316
  issn:
  - 0001-6969
publication_status: published
publisher: Springer Nature
publist_id: '7615'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Maps on probability measures preserving certain distances - a survey and some
  new results
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 84
year: '2018'
...
---
_id: '285'
abstract:
- lang: eng
  text: In graph theory, as well as in 3-manifold topology, there exist several width-type
    parameters to describe how &quot;simple&quot; or &quot;thin&quot; a given graph
    or 3-manifold is. These parameters, such as pathwidth or treewidth for graphs,
    or the concept of thin position for 3-manifolds, play an important role when studying
    algorithmic problems; in particular, there is a variety of problems in computational
    3-manifold topology - some of them known to be computationally hard in general
    - that become solvable in polynomial time as soon as the dual graph of the input
    triangulation has bounded treewidth. In view of these algorithmic results, it
    is natural to ask whether every 3-manifold admits a triangulation of bounded treewidth.
    We show that this is not the case, i.e., that there exists an infinite family
    of closed 3-manifolds not admitting triangulations of bounded pathwidth or treewidth
    (the latter implies the former, but we present two separate proofs). We derive
    these results from work of Agol and of Scharlemann and Thompson, by exhibiting
    explicit connections between the topology of a 3-manifold M on the one hand and
    width-type parameters of the dual graphs of triangulations of M on the other hand,
    answering a question that had been raised repeatedly by researchers in computational
    3-manifold topology. In particular, we show that if a closed, orientable, irreducible,
    non-Haken 3-manifold M has a triangulation of treewidth (resp. pathwidth) k then
    the Heegaard genus of M is at most 48(k+1) (resp. 4(3k+1)).
acknowledgement: Research of the second author was supported by the Einstein Foundation
  (project “Einstein Visiting Fellow Santos”) and by the Simons Foundation (“Simons
  Visiting Professors” program).
alternative_title:
- LIPIcs
article_number: '46'
article_processing_charge: No
arxiv: 1
author:
- first_name: Kristóf
  full_name: Huszár, Kristóf
  id: 33C26278-F248-11E8-B48F-1D18A9856A87
  last_name: Huszár
  orcid: 0000-0002-5445-5057
- first_name: Jonathan
  full_name: Spreer, Jonathan
  last_name: Spreer
- first_name: Uli
  full_name: Wagner, Uli
  id: 36690CA2-F248-11E8-B48F-1D18A9856A87
  last_name: Wagner
  orcid: 0000-0002-1494-0568
citation:
  ama: 'Huszár K, Spreer J, Wagner U. On the treewidth of triangulated 3-manifolds.
    In: Vol 99. Schloss Dagstuhl - Leibniz-Zentrum für Informatik; 2018. doi:<a href="https://doi.org/10.4230/LIPIcs.SoCG.2018.46">10.4230/LIPIcs.SoCG.2018.46</a>'
  apa: 'Huszár, K., Spreer, J., &#38; Wagner, U. (2018). On the treewidth of triangulated
    3-manifolds (Vol. 99). Presented at the SoCG: Symposium on Computational Geometry,
    Budapest, Hungary: Schloss Dagstuhl - Leibniz-Zentrum für Informatik. <a href="https://doi.org/10.4230/LIPIcs.SoCG.2018.46">https://doi.org/10.4230/LIPIcs.SoCG.2018.46</a>'
  chicago: Huszár, Kristóf, Jonathan Spreer, and Uli Wagner. “On the Treewidth of
    Triangulated 3-Manifolds,” Vol. 99. Schloss Dagstuhl - Leibniz-Zentrum für Informatik,
    2018. <a href="https://doi.org/10.4230/LIPIcs.SoCG.2018.46">https://doi.org/10.4230/LIPIcs.SoCG.2018.46</a>.
  ieee: 'K. Huszár, J. Spreer, and U. Wagner, “On the treewidth of triangulated 3-manifolds,”
    presented at the SoCG: Symposium on Computational Geometry, Budapest, Hungary,
    2018, vol. 99.'
  ista: 'Huszár K, Spreer J, Wagner U. 2018. On the treewidth of triangulated 3-manifolds.
    SoCG: Symposium on Computational Geometry, LIPIcs, vol. 99, 46.'
  mla: Huszár, Kristóf, et al. <i>On the Treewidth of Triangulated 3-Manifolds</i>.
    Vol. 99, 46, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2018, doi:<a href="https://doi.org/10.4230/LIPIcs.SoCG.2018.46">10.4230/LIPIcs.SoCG.2018.46</a>.
  short: K. Huszár, J. Spreer, U. Wagner, in:, Schloss Dagstuhl - Leibniz-Zentrum
    für Informatik, 2018.
conference:
  end_date: 2018-06-14
  location: Budapest, Hungary
  name: 'SoCG: Symposium on Computational Geometry'
  start_date: 2018-06-11
date_created: 2018-12-11T11:45:37Z
date_published: 2018-06-01T00:00:00Z
date_updated: 2023-09-06T11:13:41Z
day: '01'
ddc:
- '516'
- '000'
department:
- _id: UlWa
doi: 10.4230/LIPIcs.SoCG.2018.46
external_id:
  arxiv:
  - '1712.00434'
file:
- access_level: open_access
  checksum: 530d084116778135d5bffaa317479cac
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T15:32:38Z
  date_updated: 2020-07-14T12:45:51Z
  file_id: '5713'
  file_name: 2018_LIPIcs_Huszar.pdf
  file_size: 642522
  relation: main_file
file_date_updated: 2020-07-14T12:45:51Z
has_accepted_license: '1'
intvolume: '        99'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Submitted Version
publication_identifier:
  issn:
  - '18688969'
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
publist_id: '7614'
quality_controlled: '1'
related_material:
  record:
  - id: '7093'
    relation: later_version
    status: public
scopus_import: 1
status: public
title: On the treewidth of triangulated 3-manifolds
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: 99
year: '2018'
...
---
_id: '286'
abstract:
- lang: eng
  text: 'Pedigree and sibship reconstruction are important methods in quantifying
    relationships and fitness of individuals in natural populations. Current methods
    employ a Markov chain-based algorithm to explore plausible possible pedigrees
    iteratively. This provides accurate results, but is time-consuming. Here, we develop
    a method to infer sibship and paternity relationships from half-sibling arrays
    of known maternity using hierarchical clustering. Given 50 or more unlinked SNP
    markers and empirically derived error rates, the method performs as well as the
    widely used package Colony, but is faster by two orders of magnitude. Using simulations,
    we show that the method performs well across contrasting mating scenarios, even
    when samples are large. We then apply the method to open-pollinated arrays of
    the snapdragon Antirrhinum majus and find evidence for a high degree of multiple
    mating. Although we focus on diploid SNP data, the method does not depend on marker
    type and as such has broad applications in nonmodel systems. '
acknowledgement: 'ERC, Grant/Award Number: 250152'
article_processing_charge: No
author:
- first_name: Thomas
  full_name: Ellis, Thomas
  id: 3153D6D4-F248-11E8-B48F-1D18A9856A87
  last_name: Ellis
  orcid: 0000-0002-8511-0254
- first_name: David
  full_name: Field, David
  id: 419049E2-F248-11E8-B48F-1D18A9856A87
  last_name: Field
  orcid: 0000-0002-4014-8478
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: Ellis T, Field D, Barton NH. Efficient inference of paternity and sibship inference
    given known maternity via hierarchical clustering. <i>Molecular Ecology Resources</i>.
    2018;18(5):988-999. doi:<a href="https://doi.org/10.1111/1755-0998.12782">10.1111/1755-0998.12782</a>
  apa: Ellis, T., Field, D., &#38; Barton, N. H. (2018). Efficient inference of paternity
    and sibship inference given known maternity via hierarchical clustering. <i>Molecular
    Ecology Resources</i>. Wiley. <a href="https://doi.org/10.1111/1755-0998.12782">https://doi.org/10.1111/1755-0998.12782</a>
  chicago: Ellis, Thomas, David Field, and Nicholas H Barton. “Efficient Inference
    of Paternity and Sibship Inference given Known Maternity via Hierarchical Clustering.”
    <i>Molecular Ecology Resources</i>. Wiley, 2018. <a href="https://doi.org/10.1111/1755-0998.12782">https://doi.org/10.1111/1755-0998.12782</a>.
  ieee: T. Ellis, D. Field, and N. H. Barton, “Efficient inference of paternity and
    sibship inference given known maternity via hierarchical clustering,” <i>Molecular
    Ecology Resources</i>, vol. 18, no. 5. Wiley, pp. 988–999, 2018.
  ista: Ellis T, Field D, Barton NH. 2018. Efficient inference of paternity and sibship
    inference given known maternity via hierarchical clustering. Molecular Ecology
    Resources. 18(5), 988–999.
  mla: Ellis, Thomas, et al. “Efficient Inference of Paternity and Sibship Inference
    given Known Maternity via Hierarchical Clustering.” <i>Molecular Ecology Resources</i>,
    vol. 18, no. 5, Wiley, 2018, pp. 988–99, doi:<a href="https://doi.org/10.1111/1755-0998.12782">10.1111/1755-0998.12782</a>.
  short: T. Ellis, D. Field, N.H. Barton, Molecular Ecology Resources 18 (2018) 988–999.
date_created: 2018-12-11T11:45:37Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2025-05-28T11:42:43Z
day: '01'
department:
- _id: NiBa
doi: 10.1111/1755-0998.12782
ec_funded: 1
external_id:
  isi:
  - '000441753000007'
intvolume: '        18'
isi: 1
issue: '5'
language:
- iso: eng
month: '09'
oa_version: None
page: 988 - 999
project:
- _id: 25B07788-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '250152'
  name: Limits to selection in biology and in evolutionary computation
publication: Molecular Ecology Resources
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '5583'
    relation: popular_science
    status: public
scopus_import: '1'
status: public
title: Efficient inference of paternity and sibship inference given known maternity
  via hierarchical clustering
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 18
year: '2018'
...
---
_id: '287'
abstract:
- lang: eng
  text: In this paper, we discuss biological effects of electromagnetic (EM) fields
    in the context of cancer biology. In particular, we review the nanomechanical
    properties of microtubules (MTs), the latter being one of the most successful
    targets for cancer therapy. We propose an investigation on the coupling of electromagnetic
    radiation to mechanical vibrations of MTs as an important basis for biological
    and medical applications. In our opinion, optomechanical methods can accurately
    monitor and control the mechanical properties of isolated MTs in a liquid environment.
    Consequently, studying nanomechanical properties of MTs may give useful information
    for future applications to diagnostic and therapeutic technologies involving non-invasive
    externally applied physical fields. For example, electromagnetic fields or high
    intensity ultrasound can be used therapeutically avoiding harmful side effects
    of chemotherapeutic agents or classical radiation therapy.
acknowledgement: The work of SB has been supported by the European Unions Horizon
  2020 research and innovation program under the Marie Sklodowska Curie grant agreement
  No MSC-IF 707438 SUPEREOM. JAT gratefully acknowledges funding support from NSERC
  (Canada) for his research. MC acknowledges support from the Czech Science Foundation,
  projects 15-17102S and 17-11898S and he participates in COST Action BM1309, CA15211
  and bilateral exchange project between Czech and Slovak Academies of Sciences, SAV-15-22.
article_processing_charge: No
author:
- first_name: Vahid
  full_name: Salari, Vahid
  last_name: Salari
- first_name: Shabir
  full_name: Barzanjeh, Shabir
  id: 2D25E1F6-F248-11E8-B48F-1D18A9856A87
  last_name: Barzanjeh
  orcid: 0000-0003-0415-1423
- first_name: Michal
  full_name: Cifra, Michal
  last_name: Cifra
- first_name: Christoph
  full_name: Simon, Christoph
  last_name: Simon
- first_name: Felix
  full_name: Scholkmann, Felix
  last_name: Scholkmann
- first_name: Zahra
  full_name: Alirezaei, Zahra
  last_name: Alirezaei
- first_name: Jack
  full_name: Tuszynski, Jack
  last_name: Tuszynski
citation:
  ama: Salari V, Barzanjeh S, Cifra M, et al. Electromagnetic fields and optomechanics
    In cancer diagnostics and treatment. <i>Frontiers in Bioscience - Landmark</i>.
    2018;23(8):1391-1406. doi:<a href="https://doi.org/10.2741/4651">10.2741/4651</a>
  apa: Salari, V., Barzanjeh, S., Cifra, M., Simon, C., Scholkmann, F., Alirezaei,
    Z., &#38; Tuszynski, J. (2018). Electromagnetic fields and optomechanics In cancer
    diagnostics and treatment. <i>Frontiers in Bioscience - Landmark</i>. Frontiers
    in Bioscience. <a href="https://doi.org/10.2741/4651">https://doi.org/10.2741/4651</a>
  chicago: Salari, Vahid, Shabir Barzanjeh, Michal Cifra, Christoph Simon, Felix Scholkmann,
    Zahra Alirezaei, and Jack Tuszynski. “Electromagnetic Fields and Optomechanics
    In Cancer Diagnostics and Treatment.” <i>Frontiers in Bioscience - Landmark</i>.
    Frontiers in Bioscience, 2018. <a href="https://doi.org/10.2741/4651">https://doi.org/10.2741/4651</a>.
  ieee: V. Salari <i>et al.</i>, “Electromagnetic fields and optomechanics In cancer
    diagnostics and treatment,” <i>Frontiers in Bioscience - Landmark</i>, vol. 23,
    no. 8. Frontiers in Bioscience, pp. 1391–1406, 2018.
  ista: Salari V, Barzanjeh S, Cifra M, Simon C, Scholkmann F, Alirezaei Z, Tuszynski
    J. 2018. Electromagnetic fields and optomechanics In cancer diagnostics and treatment.
    Frontiers in Bioscience - Landmark. 23(8), 1391–1406.
  mla: Salari, Vahid, et al. “Electromagnetic Fields and Optomechanics In Cancer Diagnostics
    and Treatment.” <i>Frontiers in Bioscience - Landmark</i>, vol. 23, no. 8, Frontiers
    in Bioscience, 2018, pp. 1391–406, doi:<a href="https://doi.org/10.2741/4651">10.2741/4651</a>.
  short: V. Salari, S. Barzanjeh, M. Cifra, C. Simon, F. Scholkmann, Z. Alirezaei,
    J. Tuszynski, Frontiers in Bioscience - Landmark 23 (2018) 1391–1406.
date_created: 2018-12-11T11:45:37Z
date_published: 2018-03-01T00:00:00Z
date_updated: 2023-09-11T13:38:14Z
day: '01'
department:
- _id: JoFi
doi: 10.2741/4651
ec_funded: 1
external_id:
  isi:
  - '000439042800001'
  pmid:
  - '29293441'
intvolume: '        23'
isi: 1
issue: '8'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.bioscience.org/2018/v23/af/4651/fulltext.htm
month: '03'
oa: 1
oa_version: Submitted Version
page: 1391 - 1406
pmid: 1
project:
- _id: 258047B6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '707438'
  name: 'Microwave-to-Optical Quantum Link: Quantum Teleportation and Quantum Illumination
    with cavity Optomechanics SUPEREOM'
publication: Frontiers in Bioscience - Landmark
publication_status: published
publisher: Frontiers in Bioscience
quality_controlled: '1'
scopus_import: '1'
status: public
title: Electromagnetic fields and optomechanics In cancer diagnostics and treatment
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 23
year: '2018'
...
---
_id: '288'
abstract:
- lang: eng
  text: Recent lineage tracing studies have revealed that mammary gland homeostasis
    relies on unipotent stem cells. However, whether and when lineage restriction
    occurs during embryonic mammary development, and which signals orchestrate cell
    fate specification, remain unknown. Using a combination of in vivo clonal analysis
    with whole mount immunofluorescence and mathematical modelling of clonal dynamics,
    we found that embryonic multipotent mammary cells become lineage-restricted surprisingly
    early in development, with evidence for unipotency as early as E12.5 and no statistically
    discernable bipotency after E15.5. To gain insights into the mechanisms governing
    the switch from multipotency to unipotency, we used gain-of-function Notch1 mice
    and demonstrated that Notch activation cell autonomously dictates luminal cell
    fate specification to both embryonic and basally committed mammary cells. These
    functional studies have important implications for understanding the signals underlying
    cell plasticity and serve to clarify how reactivation of embryonic programs in
    adult cells can lead to cancer.
article_processing_charge: No
article_type: original
author:
- first_name: Anna
  full_name: Lilja, Anna
  last_name: Lilja
- first_name: Veronica
  full_name: Rodilla, Veronica
  last_name: Rodilla
- first_name: Mathilde
  full_name: Huyghe, Mathilde
  last_name: Huyghe
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
- first_name: Camille
  full_name: Landragin, Camille
  last_name: Landragin
- first_name: Olivier
  full_name: Renaud, Olivier
  last_name: Renaud
- first_name: Olivier
  full_name: Leroy, Olivier
  last_name: Leroy
- first_name: Steffen
  full_name: Rulands, Steffen
  last_name: Rulands
- first_name: Benjamin
  full_name: Simons, Benjamin
  last_name: Simons
- first_name: Silvia
  full_name: Fré, Silvia
  last_name: Fré
citation:
  ama: Lilja A, Rodilla V, Huyghe M, et al. Clonal analysis of Notch1-expressing cells
    reveals the existence of unipotent stem cells that retain long-term plasticity
    in the embryonic mammary gland. <i>Nature Cell Biology</i>. 2018;20(6):677-687.
    doi:<a href="https://doi.org/10.1038/s41556-018-0108-1">10.1038/s41556-018-0108-1</a>
  apa: Lilja, A., Rodilla, V., Huyghe, M., Hannezo, E. B., Landragin, C., Renaud,
    O., … Fré, S. (2018). Clonal analysis of Notch1-expressing cells reveals the existence
    of unipotent stem cells that retain long-term plasticity in the embryonic mammary
    gland. <i>Nature Cell Biology</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/s41556-018-0108-1">https://doi.org/10.1038/s41556-018-0108-1</a>
  chicago: Lilja, Anna, Veronica Rodilla, Mathilde Huyghe, Edouard B Hannezo, Camille
    Landragin, Olivier Renaud, Olivier Leroy, Steffen Rulands, Benjamin Simons, and
    Silvia Fré. “Clonal Analysis of Notch1-Expressing Cells Reveals the Existence
    of Unipotent Stem Cells That Retain Long-Term Plasticity in the Embryonic Mammary
    Gland.” <i>Nature Cell Biology</i>. Nature Publishing Group, 2018. <a href="https://doi.org/10.1038/s41556-018-0108-1">https://doi.org/10.1038/s41556-018-0108-1</a>.
  ieee: A. Lilja <i>et al.</i>, “Clonal analysis of Notch1-expressing cells reveals
    the existence of unipotent stem cells that retain long-term plasticity in the
    embryonic mammary gland,” <i>Nature Cell Biology</i>, vol. 20, no. 6. Nature Publishing
    Group, pp. 677–687, 2018.
  ista: Lilja A, Rodilla V, Huyghe M, Hannezo EB, Landragin C, Renaud O, Leroy O,
    Rulands S, Simons B, Fré S. 2018. Clonal analysis of Notch1-expressing cells reveals
    the existence of unipotent stem cells that retain long-term plasticity in the
    embryonic mammary gland. Nature Cell Biology. 20(6), 677–687.
  mla: Lilja, Anna, et al. “Clonal Analysis of Notch1-Expressing Cells Reveals the
    Existence of Unipotent Stem Cells That Retain Long-Term Plasticity in the Embryonic
    Mammary Gland.” <i>Nature Cell Biology</i>, vol. 20, no. 6, Nature Publishing
    Group, 2018, pp. 677–87, doi:<a href="https://doi.org/10.1038/s41556-018-0108-1">10.1038/s41556-018-0108-1</a>.
  short: A. Lilja, V. Rodilla, M. Huyghe, E.B. Hannezo, C. Landragin, O. Renaud, O.
    Leroy, S. Rulands, B. Simons, S. Fré, Nature Cell Biology 20 (2018) 677–687.
date_created: 2018-12-11T11:45:38Z
date_published: 2018-05-21T00:00:00Z
date_updated: 2023-09-11T12:44:08Z
day: '21'
department:
- _id: EdHa
doi: 10.1038/s41556-018-0108-1
external_id:
  isi:
  - '000433237300003'
  pmid:
  - '29784917'
intvolume: '        20'
isi: 1
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984964
month: '05'
oa: 1
oa_version: Submitted Version
page: 677 - 687
pmid: 1
publication: Nature Cell Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '7594'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Clonal analysis of Notch1-expressing cells reveals the existence of unipotent
  stem cells that retain long-term plasticity in the embryonic mammary gland
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 20
year: '2018'
...
---
_id: '289'
abstract:
- lang: eng
  text: We report on quantum capacitance measurements of high quality, graphite- and
    hexagonal boron nitride encapsulated Bernal stacked trilayer graphene devices.
    At zero applied magnetic field, we observe a number of electron density- and electrical
    displacement-tuned features in the electronic compressibility associated with
    changes in Fermi surface topology. At high displacement field and low density,
    strong trigonal warping gives rise to emergent Dirac gullies centered near the
    corners of the hexagonal Brillouin and related by three fold rotation symmetry.
    At low magnetic fields of B=1.25~T, the gullies manifest as a change in the degeneracy
    of the Landau levels from two to three. Weak incompressible states are also observed
    at integer filling within these triplets Landau levels, which a Hartree-Fock analysis
    indicates are associated with Coulomb-driven nematic phases that spontaneously
    break rotation symmetry.
acknowledgement: The experimental work at UCSB was funded by the National Science
  Foundation under Grant No. DMR- 1654186. Work at Columbia was supported by the National
  Science Foundation under Grant No. DMR- 1507788. K. W. and T. T. acknowledge support
  from the Elemental Strategy Initiative conducted by the Ministry of Education, Culture,
  Sports, Science and Technology, Japan, and the Japan Society for the Promotion of
  Science KAKENHI Grant No. JP15K21722. E. M. S. acknowledges the support of the Elings
  Fellowship from the California Nanosystems Institute at the University of California,
  Santa Barbara. A. F. Y. acknowledges the support of the David and Lucile Packard
  foundation and the Sloan Foundation. Measurements made use of a dilution refrigerator
  funded through the Major Research Instrumentation program of the U.S. National Science
  Foundation under Grant No. DMR- 1531389, and the MRL Shared Experimental Facilities,
  which are supported by the MRSEC Program of the U.S. National Science Foundation
  under Grant No. DMR- 1720256.
article_number: '167601'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Alexander
  full_name: Zibrov, Alexander
  last_name: Zibrov
- first_name: Rao
  full_name: Peng, Rao
  id: 47C23AC6-02D0-11E9-BD0E-99399A5D3DEB
  last_name: Peng
  orcid: 0000-0003-1250-0021
- first_name: Carlos
  full_name: Kometter, Carlos
  last_name: Kometter
- first_name: Jia
  full_name: Li, Jia
  last_name: Li
- first_name: Cory
  full_name: Dean, Cory
  last_name: Dean
- first_name: Takashi
  full_name: Taniguchi, Takashi
  last_name: Taniguchi
- first_name: Kenji
  full_name: Watanabe, Kenji
  last_name: Watanabe
- first_name: Maksym
  full_name: Serbyn, Maksym
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
- first_name: Andrea
  full_name: Young, Andrea
  last_name: Young
citation:
  ama: Zibrov A, Rao P, Kometter C, et al. Emergent dirac gullies and gully-symmetry-breaking
    quantum hall states in ABA trilayer graphene. <i>Physical Review Letters</i>.
    2018;121(16). doi:<a href="https://doi.org/10.1103/PhysRevLett.121.167601">10.1103/PhysRevLett.121.167601</a>
  apa: Zibrov, A., Rao, P., Kometter, C., Li, J., Dean, C., Taniguchi, T., … Young,
    A. (2018). Emergent dirac gullies and gully-symmetry-breaking quantum hall states
    in ABA trilayer graphene. <i>Physical Review Letters</i>. American Physical Society.
    <a href="https://doi.org/10.1103/PhysRevLett.121.167601">https://doi.org/10.1103/PhysRevLett.121.167601</a>
  chicago: Zibrov, Alexander, Peng Rao, Carlos Kometter, Jia Li, Cory Dean, Takashi
    Taniguchi, Kenji Watanabe, Maksym Serbyn, and Andrea Young. “Emergent Dirac Gullies
    and Gully-Symmetry-Breaking Quantum Hall States in ABA Trilayer Graphene.” <i>Physical
    Review Letters</i>. American Physical Society, 2018. <a href="https://doi.org/10.1103/PhysRevLett.121.167601">https://doi.org/10.1103/PhysRevLett.121.167601</a>.
  ieee: A. Zibrov <i>et al.</i>, “Emergent dirac gullies and gully-symmetry-breaking
    quantum hall states in ABA trilayer graphene,” <i>Physical Review Letters</i>,
    vol. 121, no. 16. American Physical Society, 2018.
  ista: Zibrov A, Rao P, Kometter C, Li J, Dean C, Taniguchi T, Watanabe K, Serbyn
    M, Young A. 2018. Emergent dirac gullies and gully-symmetry-breaking quantum hall
    states in ABA trilayer graphene. Physical Review Letters. 121(16), 167601.
  mla: Zibrov, Alexander, et al. “Emergent Dirac Gullies and Gully-Symmetry-Breaking
    Quantum Hall States in ABA Trilayer Graphene.” <i>Physical Review Letters</i>,
    vol. 121, no. 16, 167601, American Physical Society, 2018, doi:<a href="https://doi.org/10.1103/PhysRevLett.121.167601">10.1103/PhysRevLett.121.167601</a>.
  short: A. Zibrov, P. Rao, C. Kometter, J. Li, C. Dean, T. Taniguchi, K. Watanabe,
    M. Serbyn, A. Young, Physical Review Letters 121 (2018).
date_created: 2018-12-11T11:45:38Z
date_published: 2018-10-19T00:00:00Z
date_updated: 2023-09-11T13:39:50Z
day: '19'
department:
- _id: MaSe
doi: 10.1103/PhysRevLett.121.167601
external_id:
  arxiv:
  - '1805.01038'
  isi:
  - '000447307500007'
intvolume: '       121'
isi: 1
issue: '16'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1805.01038
month: '10'
oa: 1
oa_version: Preprint
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Emergent dirac gullies and gully-symmetry-breaking quantum hall states in ABA
  trilayer graphene
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 121
year: '2018'
...
---
_id: '29'
abstract:
- lang: eng
  text: Social insects have evolved enormous capacities to collectively build nests
    and defend their colonies against both predators and pathogens. The latter is
    achieved by a combination of individual immune responses and sophisticated collective
    behavioral and organizational disease defenses, that is, social immunity. We investigated
    how the presence or absence of these social defense lines affects individual-level
    immunity in ant queens after bacterial infection. To this end, we injected queens
    of the ant Linepithema humile with a mix of gram+ and gram− bacteria or a control
    solution, reared them either with workers or alone and analyzed their gene expression
    patterns at 2, 4, 8, and 12 hr post-injection, using RNA-seq. This allowed us
    to test for the effect of bacterial infection, social context, as well as the
    interaction between the two over the course of infection and raising of an immune
    response. We found that social isolation per se affected queen gene expression
    for metabolism genes, but not for immune genes. When infected, queens reared with
    and without workers up-regulated similar numbers of innate immune genes revealing
    activation of Toll and Imd signaling pathways and melanization. Interestingly,
    however, they mostly regulated different genes along the pathways and showed a
    different pattern of overall gene up-regulation or down-regulation. Hence, we
    can conclude that the absence of workers does not compromise the onset of an individual
    immune response by the queens, but that the social environment impacts the route
    of the individual innate immune responses.
article_processing_charge: No
author:
- first_name: Lumi
  full_name: Viljakainen, Lumi
  last_name: Viljakainen
- first_name: Jaana
  full_name: Jurvansuu, Jaana
  last_name: Jurvansuu
- first_name: Ida
  full_name: Holmberg, Ida
  last_name: Holmberg
- first_name: Tobias
  full_name: Pamminger, Tobias
  last_name: Pamminger
- first_name: Silvio
  full_name: Erler, Silvio
  last_name: Erler
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
citation:
  ama: Viljakainen L, Jurvansuu J, Holmberg I, Pamminger T, Erler S, Cremer S. Social
    environment affects the transcriptomic response to bacteria in ant queens. <i>Ecology
    and Evolution</i>. 2018;8(22):11031-11070. doi:<a href="https://doi.org/10.1002/ece3.4573">10.1002/ece3.4573</a>
  apa: Viljakainen, L., Jurvansuu, J., Holmberg, I., Pamminger, T., Erler, S., &#38;
    Cremer, S. (2018). Social environment affects the transcriptomic response to bacteria
    in ant queens. <i>Ecology and Evolution</i>. Wiley. <a href="https://doi.org/10.1002/ece3.4573">https://doi.org/10.1002/ece3.4573</a>
  chicago: Viljakainen, Lumi, Jaana Jurvansuu, Ida Holmberg, Tobias Pamminger, Silvio
    Erler, and Sylvia Cremer. “Social Environment Affects the Transcriptomic Response
    to Bacteria in Ant Queens.” <i>Ecology and Evolution</i>. Wiley, 2018. <a href="https://doi.org/10.1002/ece3.4573">https://doi.org/10.1002/ece3.4573</a>.
  ieee: L. Viljakainen, J. Jurvansuu, I. Holmberg, T. Pamminger, S. Erler, and S.
    Cremer, “Social environment affects the transcriptomic response to bacteria in
    ant queens,” <i>Ecology and Evolution</i>, vol. 8, no. 22. Wiley, pp. 11031–11070,
    2018.
  ista: Viljakainen L, Jurvansuu J, Holmberg I, Pamminger T, Erler S, Cremer S. 2018.
    Social environment affects the transcriptomic response to bacteria in ant queens.
    Ecology and Evolution. 8(22), 11031–11070.
  mla: Viljakainen, Lumi, et al. “Social Environment Affects the Transcriptomic Response
    to Bacteria in Ant Queens.” <i>Ecology and Evolution</i>, vol. 8, no. 22, Wiley,
    2018, pp. 11031–70, doi:<a href="https://doi.org/10.1002/ece3.4573">10.1002/ece3.4573</a>.
  short: L. Viljakainen, J. Jurvansuu, I. Holmberg, T. Pamminger, S. Erler, S. Cremer,
    Ecology and Evolution 8 (2018) 11031–11070.
date_created: 2018-12-11T11:44:15Z
date_published: 2018-11-01T00:00:00Z
date_updated: 2023-09-19T09:29:12Z
day: '01'
ddc:
- '576'
- '591'
department:
- _id: SyCr
doi: 10.1002/ece3.4573
external_id:
  isi:
  - '000451611000032'
file:
- access_level: open_access
  checksum: 0d1355c78627ca7210aadd9a17a01915
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T08:27:04Z
  date_updated: 2020-07-14T12:45:52Z
  file_id: '5682'
  file_name: Viljakainen_et_al-2018-Ecology_and_Evolution.pdf
  file_size: 1272096
  relation: main_file
file_date_updated: 2020-07-14T12:45:52Z
has_accepted_license: '1'
intvolume: '         8'
isi: 1
issue: '22'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 11031-11070
publication: Ecology and Evolution
publication_identifier:
  issn:
  - '20457758'
publication_status: published
publisher: Wiley
publist_id: '8026'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Social environment affects the transcriptomic response to bacteria in ant queens
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 8
year: '2018'
...
---
_id: '291'
abstract:
- lang: eng
  text: Over the past decade, the edge of chaos has proven to be a fruitful starting
    point for investigations of shear flows when the laminar base flow is linearly
    stable. Numerous computational studies of shear flows demonstrated the existence
    of states that separate laminar and turbulent regions of the state space. In addition,
    some studies determined invariant solutions that reside on this edge. In this
    paper, we study the unstable manifold of one such solution with the aid of continuous
    symmetry reduction, which we formulate here for the simultaneous quotiening of
    axial and azimuthal symmetries. Upon our investigation of the unstable manifold,
    we discover a previously unknown traveling-wave solution on the laminar-turbulent
    boundary with a relatively complex structure. By means of low-dimensional projections,
    we visualize different dynamical paths that connect these solutions to the turbulence.
    Our numerical experiments demonstrate that the laminar-turbulent boundary exhibits
    qualitatively different regions whose properties are influenced by the nearby
    invariant solutions.
article_number: '054401'
article_processing_charge: No
arxiv: 1
author:
- first_name: Nazmi B
  full_name: Budanur, Nazmi B
  id: 3EA1010E-F248-11E8-B48F-1D18A9856A87
  last_name: Budanur
  orcid: 0000-0003-0423-5010
- first_name: Björn
  full_name: Hof, Björn
  id: 3A374330-F248-11E8-B48F-1D18A9856A87
  last_name: Hof
  orcid: 0000-0003-2057-2754
citation:
  ama: Budanur NB, Hof B. Complexity of the laminar-turbulent boundary in pipe flow.
    <i>Physical Review Fluids</i>. 2018;3(5). doi:<a href="https://doi.org/10.1103/PhysRevFluids.3.054401">10.1103/PhysRevFluids.3.054401</a>
  apa: Budanur, N. B., &#38; Hof, B. (2018). Complexity of the laminar-turbulent boundary
    in pipe flow. <i>Physical Review Fluids</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevFluids.3.054401">https://doi.org/10.1103/PhysRevFluids.3.054401</a>
  chicago: Budanur, Nazmi B, and Björn Hof. “Complexity of the Laminar-Turbulent Boundary
    in Pipe Flow.” <i>Physical Review Fluids</i>. American Physical Society, 2018.
    <a href="https://doi.org/10.1103/PhysRevFluids.3.054401">https://doi.org/10.1103/PhysRevFluids.3.054401</a>.
  ieee: N. B. Budanur and B. Hof, “Complexity of the laminar-turbulent boundary in
    pipe flow,” <i>Physical Review Fluids</i>, vol. 3, no. 5. American Physical Society,
    2018.
  ista: Budanur NB, Hof B. 2018. Complexity of the laminar-turbulent boundary in pipe
    flow. Physical Review Fluids. 3(5), 054401.
  mla: Budanur, Nazmi B., and Björn Hof. “Complexity of the Laminar-Turbulent Boundary
    in Pipe Flow.” <i>Physical Review Fluids</i>, vol. 3, no. 5, 054401, American
    Physical Society, 2018, doi:<a href="https://doi.org/10.1103/PhysRevFluids.3.054401">10.1103/PhysRevFluids.3.054401</a>.
  short: N.B. Budanur, B. Hof, Physical Review Fluids 3 (2018).
date_created: 2018-12-11T11:45:39Z
date_published: 2018-05-30T00:00:00Z
date_updated: 2023-09-11T12:45:44Z
day: '30'
department:
- _id: BjHo
doi: 10.1103/PhysRevFluids.3.054401
external_id:
  arxiv:
  - '1802.01918'
  isi:
  - '000433426200001'
intvolume: '         3'
isi: 1
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1802.01918
month: '05'
oa: 1
oa_version: Preprint
publication: Physical Review Fluids
publication_status: published
publisher: American Physical Society
publist_id: '7590'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Complexity of the laminar-turbulent boundary in pipe flow
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 3
year: '2018'
...
---
_id: '292'
abstract:
- lang: eng
  text: 'Retina is a paradigmatic system for studying sensory encoding: the transformation
    of light into spiking activity of ganglion cells. The inverse problem, where stimulus
    is reconstructed from spikes, has received less attention, especially for complex
    stimuli that should be reconstructed “pixel-by-pixel”. We recorded around a hundred
    neurons from a dense patch in a rat retina and decoded movies of multiple small
    randomly-moving discs. We constructed nonlinear (kernelized and neural network)
    decoders that improved significantly over linear results. An important contribution
    to this was the ability of nonlinear decoders to reliably separate between neural
    responses driven by locally fluctuating light signals, and responses at locally
    constant light driven by spontaneous-like activity. This improvement crucially
    depended on the precise, non-Poisson temporal structure of individual spike trains,
    which originated in the spike-history dependence of neural responses. We propose
    a general principle by which downstream circuitry could discriminate between spontaneous
    and stimulus-driven activity based solely on higher-order statistical structure
    in the incoming spike trains.'
article_number: e1006057
article_processing_charge: Yes
article_type: original
author:
- first_name: Vicent
  full_name: Botella Soler, Vicent
  id: 421234E8-F248-11E8-B48F-1D18A9856A87
  last_name: Botella Soler
  orcid: 0000-0002-8790-1914
- first_name: Stephane
  full_name: Deny, Stephane
  last_name: Deny
- first_name: Georg S
  full_name: Martius, Georg S
  last_name: Martius
- first_name: Olivier
  full_name: Marre, Olivier
  last_name: Marre
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
citation:
  ama: Botella Soler V, Deny S, Martius GS, Marre O, Tkačik G. Nonlinear decoding
    of a complex movie from the mammalian retina. <i>PLoS Computational Biology</i>.
    2018;14(5). doi:<a href="https://doi.org/10.1371/journal.pcbi.1006057">10.1371/journal.pcbi.1006057</a>
  apa: Botella Soler, V., Deny, S., Martius, G. S., Marre, O., &#38; Tkačik, G. (2018).
    Nonlinear decoding of a complex movie from the mammalian retina. <i>PLoS Computational
    Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pcbi.1006057">https://doi.org/10.1371/journal.pcbi.1006057</a>
  chicago: Botella Soler, Vicente, Stephane Deny, Georg S Martius, Olivier Marre,
    and Gašper Tkačik. “Nonlinear Decoding of a Complex Movie from the Mammalian Retina.”
    <i>PLoS Computational Biology</i>. Public Library of Science, 2018. <a href="https://doi.org/10.1371/journal.pcbi.1006057">https://doi.org/10.1371/journal.pcbi.1006057</a>.
  ieee: V. Botella Soler, S. Deny, G. S. Martius, O. Marre, and G. Tkačik, “Nonlinear
    decoding of a complex movie from the mammalian retina,” <i>PLoS Computational
    Biology</i>, vol. 14, no. 5. Public Library of Science, 2018.
  ista: Botella Soler V, Deny S, Martius GS, Marre O, Tkačik G. 2018. Nonlinear decoding
    of a complex movie from the mammalian retina. PLoS Computational Biology. 14(5),
    e1006057.
  mla: Botella Soler, Vicente, et al. “Nonlinear Decoding of a Complex Movie from
    the Mammalian Retina.” <i>PLoS Computational Biology</i>, vol. 14, no. 5, e1006057,
    Public Library of Science, 2018, doi:<a href="https://doi.org/10.1371/journal.pcbi.1006057">10.1371/journal.pcbi.1006057</a>.
  short: V. Botella Soler, S. Deny, G.S. Martius, O. Marre, G. Tkačik, PLoS Computational
    Biology 14 (2018).
date_created: 2018-12-11T11:45:39Z
date_published: 2018-05-10T00:00:00Z
date_updated: 2024-02-21T13:45:25Z
day: '10'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1371/journal.pcbi.1006057
ec_funded: 1
external_id:
  isi:
  - '000434012100002'
file:
- access_level: open_access
  checksum: 3026f94d235219e15514505fdbadf34e
  content_type: application/pdf
  creator: dernst
  date_created: 2019-02-13T11:07:15Z
  date_updated: 2020-07-14T12:45:53Z
  file_id: '5974'
  file_name: 2018_Plos_Botella_Soler.pdf
  file_size: 3460786
  relation: main_file
file_date_updated: 2020-07-14T12:45:53Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
issue: '5'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
project:
- _id: 25CBA828-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '720270'
  name: Human Brain Project Specific Grant Agreement 1 (HBP SGA 1)
- _id: 254D1A94-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 25651-N26
  name: Sensitivity to higher-order statistics in natural scenes
publication: PLoS Computational Biology
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  link:
  - description: News on IST Homepage
    relation: press_release
    url: https://ist.ac.at/en/news/video-of-moving-discs-reconstructed-from-rat-retinal-neuron-signals/
  record:
  - id: '5584'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Nonlinear decoding of a complex movie from the mammalian retina
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2018'
...
---
_id: '293'
abstract:
- lang: eng
  text: People sometimes make their admirable deeds and accomplishments hard to spot,
    such as by giving anonymously or avoiding bragging. Such ‘buried’ signals are
    hard to reconcile with standard models of signalling or indirect reciprocity,
    which motivate costly pro-social behaviour by reputational gains. To explain these
    phenomena, we design a simple game theory model, which we call the signal-burying
    game. This game has the feature that senders can bury their signal by deliberately
    reducing the probability of the signal being observed. If the signal is observed,
    however, it is identified as having been buried. We show under which conditions
    buried signals can be maintained, using static equilibrium concepts and calculations
    of the evolutionary dynamics. We apply our analysis to shed light on a number
    of otherwise puzzling social phenomena, including modesty, anonymous donations,
    subtlety in art and fashion, and overeagerness.
acknowledgement: This work was supported by a grant from the John Templeton Foundation
  and by the Office of Naval Research Grant N00014-16-1-2914 (M.A.N.). C.H. acknowledges
  generous support from the ISTFELLOW programme and by the Schrödinger scholarship
  of the Austrian Science Fund (FWF) J3475.
article_processing_charge: No
article_type: original
author:
- first_name: Moshe
  full_name: Hoffman, Moshe
  last_name: Hoffman
- first_name: Christian
  full_name: Hilbe, Christian
  id: 2FDF8F3C-F248-11E8-B48F-1D18A9856A87
  last_name: Hilbe
  orcid: 0000-0001-5116-955X
- first_name: Martin
  full_name: Nowak, Martin
  last_name: Nowak
citation:
  ama: Hoffman M, Hilbe C, Nowak M. The signal-burying game can explain why we obscure
    positive traits and good deeds. <i>Nature Human Behaviour</i>. 2018;2:397-404.
    doi:<a href="https://doi.org/10.1038/s41562-018-0354-z">10.1038/s41562-018-0354-z</a>
  apa: Hoffman, M., Hilbe, C., &#38; Nowak, M. (2018). The signal-burying game can
    explain why we obscure positive traits and good deeds. <i>Nature Human Behaviour</i>.
    Nature Publishing Group. <a href="https://doi.org/10.1038/s41562-018-0354-z">https://doi.org/10.1038/s41562-018-0354-z</a>
  chicago: Hoffman, Moshe, Christian Hilbe, and Martin Nowak. “The Signal-Burying
    Game Can Explain Why We Obscure Positive Traits and Good Deeds.” <i>Nature Human
    Behaviour</i>. Nature Publishing Group, 2018. <a href="https://doi.org/10.1038/s41562-018-0354-z">https://doi.org/10.1038/s41562-018-0354-z</a>.
  ieee: M. Hoffman, C. Hilbe, and M. Nowak, “The signal-burying game can explain why
    we obscure positive traits and good deeds,” <i>Nature Human Behaviour</i>, vol.
    2. Nature Publishing Group, pp. 397–404, 2018.
  ista: Hoffman M, Hilbe C, Nowak M. 2018. The signal-burying game can explain why
    we obscure positive traits and good deeds. Nature Human Behaviour. 2, 397–404.
  mla: Hoffman, Moshe, et al. “The Signal-Burying Game Can Explain Why We Obscure
    Positive Traits and Good Deeds.” <i>Nature Human Behaviour</i>, vol. 2, Nature
    Publishing Group, 2018, pp. 397–404, doi:<a href="https://doi.org/10.1038/s41562-018-0354-z">10.1038/s41562-018-0354-z</a>.
  short: M. Hoffman, C. Hilbe, M. Nowak, Nature Human Behaviour 2 (2018) 397–404.
date_created: 2018-12-11T11:45:39Z
date_published: 2018-05-28T00:00:00Z
date_updated: 2023-09-19T10:12:03Z
day: '28'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1038/s41562-018-0354-z
ec_funded: 1
external_id:
  isi:
  - '000435551300009'
file:
- access_level: open_access
  checksum: 32efaf06a597495c184df91b3fbb19c0
  content_type: application/pdf
  creator: dernst
  date_created: 2019-11-19T08:17:23Z
  date_updated: 2020-07-14T12:45:54Z
  file_id: '7051'
  file_name: 2018_NatureHumanBeh_Hoffman.pdf
  file_size: 194734
  relation: main_file
file_date_updated: 2020-07-14T12:45:54Z
has_accepted_license: '1'
intvolume: '         2'
isi: 1
language:
- iso: eng
month: '05'
oa: 1
oa_version: Submitted Version
page: 397 - 404
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: Nature Human Behaviour
publication_status: published
publisher: Nature Publishing Group
publist_id: '7588'
quality_controlled: '1'
related_material:
  link:
  - description: News on IST Homepage
    relation: press_release
    url: https://ist.ac.at/en/news/the-logic-of-modesty-why-it-pays-to-be-humble/
scopus_import: '1'
status: public
title: The signal-burying game can explain why we obscure positive traits and good
  deeds
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 2
year: '2018'
...
---
_id: '294'
abstract:
- lang: eng
  text: We developed a method to calculate two-photon processes in quantum mechanics
    that replaces the infinite summation over the intermediate states by a perturbation
    expansion. This latter consists of a series of commutators that involve position,
    momentum, and Hamiltonian quantum operators. We analyzed several single- and many-particle
    cases for which a closed-form solution to the perturbation expansion exists, as
    well as more complicated cases for which a solution is found by convergence. Throughout
    the article, Rayleigh and Raman scattering are taken as examples of two-photon
    processes. The present method provides a clear distinction between the Thomson
    scattering, regarded as classical scattering, and quantum contributions. Such
    a distinction lets us derive general results concerning light scattering. Finally,
    possible extensions to the developed formalism are discussed.
article_processing_charge: No
arxiv: 1
author:
- first_name: Filippo
  full_name: Fratini, Filippo
  last_name: Fratini
- first_name: Laleh
  full_name: Safari, Laleh
  id: 3C325E5E-F248-11E8-B48F-1D18A9856A87
  last_name: Safari
- first_name: Pedro
  full_name: Amaro, Pedro
  last_name: Amaro
- first_name: José
  full_name: Santos, José
  last_name: Santos
citation:
  ama: Fratini F, Safari L, Amaro P, Santos J. Two-photon processes based on quantum
    commutators. <i>Physical Review A - Atomic, Molecular, and Optical Physics</i>.
    2018;97(4). doi:<a href="https://doi.org/10.1103/PhysRevA.97.043842">10.1103/PhysRevA.97.043842</a>
  apa: Fratini, F., Safari, L., Amaro, P., &#38; Santos, J. (2018). Two-photon processes
    based on quantum commutators. <i>Physical Review A - Atomic, Molecular, and Optical
    Physics</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevA.97.043842">https://doi.org/10.1103/PhysRevA.97.043842</a>
  chicago: Fratini, Filippo, Laleh Safari, Pedro Amaro, and José Santos. “Two-Photon
    Processes Based on Quantum Commutators.” <i>Physical Review A - Atomic, Molecular,
    and Optical Physics</i>. American Physical Society, 2018. <a href="https://doi.org/10.1103/PhysRevA.97.043842">https://doi.org/10.1103/PhysRevA.97.043842</a>.
  ieee: F. Fratini, L. Safari, P. Amaro, and J. Santos, “Two-photon processes based
    on quantum commutators,” <i>Physical Review A - Atomic, Molecular, and Optical
    Physics</i>, vol. 97, no. 4. American Physical Society, 2018.
  ista: Fratini F, Safari L, Amaro P, Santos J. 2018. Two-photon processes based on
    quantum commutators. Physical Review A - Atomic, Molecular, and Optical Physics.
    97(4).
  mla: Fratini, Filippo, et al. “Two-Photon Processes Based on Quantum Commutators.”
    <i>Physical Review A - Atomic, Molecular, and Optical Physics</i>, vol. 97, no.
    4, American Physical Society, 2018, doi:<a href="https://doi.org/10.1103/PhysRevA.97.043842">10.1103/PhysRevA.97.043842</a>.
  short: F. Fratini, L. Safari, P. Amaro, J. Santos, Physical Review A - Atomic, Molecular,
    and Optical Physics 97 (2018).
date_created: 2018-12-11T11:45:40Z
date_published: 2018-04-18T00:00:00Z
date_updated: 2023-09-19T10:17:56Z
day: '18'
department:
- _id: MiLe
doi: 10.1103/PhysRevA.97.043842
ec_funded: 1
external_id:
  arxiv:
  - '1801.06892'
  isi:
  - '000430296800008'
intvolume: '        97'
isi: 1
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1801.06892
month: '04'
oa: 1
oa_version: Submitted Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: Physical Review A - Atomic, Molecular, and Optical Physics
publication_status: published
publisher: American Physical Society
publist_id: '7587'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Two-photon processes based on quantum commutators
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 97
year: '2018'
...
---
_id: '295'
abstract:
- lang: eng
  text: We prove upper and lower bounds on the ground-state energy of the ideal two-dimensional
    anyon gas. Our bounds are extensive in the particle number, as for fermions, and
    linear in the statistics parameter (Formula presented.). The lower bounds extend
    to Lieb–Thirring inequalities for all anyons except bosons.
acknowledgement: Financial support from the Swedish Research Council, grant no. 2013-4734
  (D. L.), the European Research Council (ERC) under the European Union’s Horizon
  2020 research and innovation programme (grant agreement No 694227, R. S.), and by
  the Austrian Science Fund (FWF), project Nr. P 27533-N27 (R. S.), is gratefully
  acknowledged.
article_processing_charge: No
arxiv: 1
author:
- first_name: Douglas
  full_name: Lundholm, Douglas
  last_name: Lundholm
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
citation:
  ama: Lundholm D, Seiringer R. Fermionic behavior of ideal anyons. <i>Letters in
    Mathematical Physics</i>. 2018;108(11):2523-2541. doi:<a href="https://doi.org/10.1007/s11005-018-1091-y">10.1007/s11005-018-1091-y</a>
  apa: Lundholm, D., &#38; Seiringer, R. (2018). Fermionic behavior of ideal anyons.
    <i>Letters in Mathematical Physics</i>. Springer. <a href="https://doi.org/10.1007/s11005-018-1091-y">https://doi.org/10.1007/s11005-018-1091-y</a>
  chicago: Lundholm, Douglas, and Robert Seiringer. “Fermionic Behavior of Ideal Anyons.”
    <i>Letters in Mathematical Physics</i>. Springer, 2018. <a href="https://doi.org/10.1007/s11005-018-1091-y">https://doi.org/10.1007/s11005-018-1091-y</a>.
  ieee: D. Lundholm and R. Seiringer, “Fermionic behavior of ideal anyons,” <i>Letters
    in Mathematical Physics</i>, vol. 108, no. 11. Springer, pp. 2523–2541, 2018.
  ista: Lundholm D, Seiringer R. 2018. Fermionic behavior of ideal anyons. Letters
    in Mathematical Physics. 108(11), 2523–2541.
  mla: Lundholm, Douglas, and Robert Seiringer. “Fermionic Behavior of Ideal Anyons.”
    <i>Letters in Mathematical Physics</i>, vol. 108, no. 11, Springer, 2018, pp.
    2523–41, doi:<a href="https://doi.org/10.1007/s11005-018-1091-y">10.1007/s11005-018-1091-y</a>.
  short: D. Lundholm, R. Seiringer, Letters in Mathematical Physics 108 (2018) 2523–2541.
date_created: 2018-12-11T11:45:40Z
date_published: 2018-05-11T00:00:00Z
date_updated: 2023-09-11T14:01:57Z
day: '11'
ddc:
- '510'
department:
- _id: RoSe
doi: 10.1007/s11005-018-1091-y
ec_funded: 1
external_id:
  arxiv:
  - '1712.06218'
  isi:
  - '000446491500008'
file:
- access_level: open_access
  checksum: 8beb9632fa41bbd19452f55f31286a31
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T12:14:17Z
  date_updated: 2020-07-14T12:45:55Z
  file_id: '5698'
  file_name: 2018_LettMathPhys_Lundholm.pdf
  file_size: 551996
  relation: main_file
file_date_updated: 2020-07-14T12:45:55Z
has_accepted_license: '1'
intvolume: '       108'
isi: 1
issue: '11'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 2523-2541
project:
- _id: 25C6DC12-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '694227'
  name: Analysis of quantum many-body systems
- _id: 25C878CE-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P27533_N27
  name: Structure of the Excitation Spectrum for Many-Body Quantum Systems
publication: Letters in Mathematical Physics
publication_status: published
publisher: Springer
publist_id: '7586'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fermionic behavior of ideal anyons
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 108
year: '2018'
...
---
_id: '296'
abstract:
- lang: eng
  text: The thermodynamic description of many-particle systems rests on the assumption
    of ergodicity, the ability of a system to explore all allowed configurations in
    the phase space. Recent studies on many-body localization have revealed the existence
    of systems that strongly violate ergodicity in the presence of quenched disorder.
    Here, we demonstrate that ergodicity can be weakly broken by a different mechanism,
    arising from the presence of special eigenstates in the many-body spectrum that
    are reminiscent of quantum scars in chaotic non-interacting systems. In the single-particle
    case, quantum scars correspond to wavefunctions that concentrate in the vicinity
    of unstable periodic classical trajectories. We show that many-body scars appear
    in the Fibonacci chain, a model with a constrained local Hilbert space that has
    recently been experimentally realized in a Rydberg-atom quantum simulator. The
    quantum scarred eigenstates are embedded throughout the otherwise thermalizing
    many-body spectrum but lead to direct experimental signatures, as we show for
    periodic recurrences that reproduce those observed in the experiment. Our results
    suggest that scarred many-body bands give rise to a new universality class of
    quantum dynamics, opening up opportunities for the creation of novel states with
    long-lived coherence in systems that are now experimentally realizable.
acknowledgement: C.J.T., A.M. and Z.P. acknowledge support from EPSRC grants EP/P009409/1
  and EP/M50807X/1, and Royal Society Research Grant RG160635. D.A. acknowledges support
  from the Swiss National Science Foundation.
article_processing_charge: No
article_type: original
author:
- first_name: Christopher
  full_name: Turner, Christopher
  last_name: Turner
- first_name: Alexios
  full_name: Michailidis, Alexios
  id: 36EBAD38-F248-11E8-B48F-1D18A9856A87
  last_name: Michailidis
  orcid: 0000-0002-8443-1064
- first_name: Dmitry
  full_name: Abanin, Dmitry
  last_name: Abanin
- first_name: Maksym
  full_name: Serbyn, Maksym
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
- first_name: Zlatko
  full_name: Papić, Zlatko
  last_name: Papić
citation:
  ama: Turner C, Michailidis A, Abanin D, Serbyn M, Papić Z. Weak ergodicity breaking
    from quantum many-body scars. <i>Nature Physics</i>. 2018;14:745-749. doi:<a href="https://doi.org/10.1038/s41567-018-0137-5">10.1038/s41567-018-0137-5</a>
  apa: Turner, C., Michailidis, A., Abanin, D., Serbyn, M., &#38; Papić, Z. (2018).
    Weak ergodicity breaking from quantum many-body scars. <i>Nature Physics</i>.
    Nature Publishing Group. <a href="https://doi.org/10.1038/s41567-018-0137-5">https://doi.org/10.1038/s41567-018-0137-5</a>
  chicago: Turner, Christopher, Alexios Michailidis, Dmitry Abanin, Maksym Serbyn,
    and Zlatko Papić. “Weak Ergodicity Breaking from Quantum Many-Body Scars.” <i>Nature
    Physics</i>. Nature Publishing Group, 2018. <a href="https://doi.org/10.1038/s41567-018-0137-5">https://doi.org/10.1038/s41567-018-0137-5</a>.
  ieee: C. Turner, A. Michailidis, D. Abanin, M. Serbyn, and Z. Papić, “Weak ergodicity
    breaking from quantum many-body scars,” <i>Nature Physics</i>, vol. 14. Nature
    Publishing Group, pp. 745–749, 2018.
  ista: Turner C, Michailidis A, Abanin D, Serbyn M, Papić Z. 2018. Weak ergodicity
    breaking from quantum many-body scars. Nature Physics. 14, 745–749.
  mla: Turner, Christopher, et al. “Weak Ergodicity Breaking from Quantum Many-Body
    Scars.” <i>Nature Physics</i>, vol. 14, Nature Publishing Group, 2018, pp. 745–49,
    doi:<a href="https://doi.org/10.1038/s41567-018-0137-5">10.1038/s41567-018-0137-5</a>.
  short: C. Turner, A. Michailidis, D. Abanin, M. Serbyn, Z. Papić, Nature Physics
    14 (2018) 745–749.
date_created: 2018-12-11T11:45:40Z
date_published: 2018-05-14T00:00:00Z
date_updated: 2023-09-19T10:37:55Z
day: '14'
department:
- _id: MaSe
doi: 10.1038/s41567-018-0137-5
external_id:
  isi:
  - '000438253600028'
intvolume: '        14'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://eprints.whiterose.ac.uk/130860/
month: '05'
oa: 1
oa_version: Submitted Version
page: 745 - 749
publication: Nature Physics
publication_status: published
publisher: Nature Publishing Group
publist_id: '7585'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Weak ergodicity breaking from quantum many-body scars
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2018'
...
---
_id: '297'
abstract:
- lang: eng
  text: Graph games played by two players over finite-state graphs are central in
    many problems in computer science. In particular, graph games with ω -regular
    winning conditions, specified as parity objectives, which can express properties
    such as safety, liveness, fairness, are the basic framework for verification and
    synthesis of reactive systems. The decisions for a player at various states of
    the graph game are represented as strategies. While the algorithmic problem for
    solving graph games with parity objectives has been widely studied, the most prominent
    data-structure for strategy representation in graph games has been binary decision
    diagrams (BDDs). However, due to the bit-level representation, BDDs do not retain
    the inherent flavor of the decisions of strategies, and are notoriously hard to
    minimize to obtain succinct representation. In this work we propose decision trees
    for strategy representation in graph games. Decision trees retain the flavor of
    decisions of strategies and allow entropy-based minimization to obtain succinct
    trees. However, decision trees work in settings (e.g., probabilistic models) where
    errors are allowed, and overfitting of data is typically avoided. In contrast,
    for strategies in graph games no error is allowed, and the decision tree must
    represent the entire strategy. We develop new techniques to extend decision trees
    to overcome the above obstacles, while retaining the entropy-based techniques
    to obtain succinct trees. We have implemented our techniques to extend the existing
    decision tree solvers. We present experimental results for problems in reactive
    synthesis to show that decision trees provide a much more efficient data-structure
    for strategy representation as compared to BDDs.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Tomáš
  full_name: Brázdil, Tomáš
  last_name: Brázdil
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Jan
  full_name: Kretinsky, Jan
  id: 44CEF464-F248-11E8-B48F-1D18A9856A87
  last_name: Kretinsky
  orcid: 0000-0002-8122-2881
- first_name: Viktor
  full_name: Toman, Viktor
  id: 3AF3DA7C-F248-11E8-B48F-1D18A9856A87
  last_name: Toman
  orcid: 0000-0001-9036-063X
citation:
  ama: 'Brázdil T, Chatterjee K, Kretinsky J, Toman V. Strategy representation by
    decision trees in reactive synthesis. In: Vol 10805. Springer; 2018:385-407. doi:<a
    href="https://doi.org/10.1007/978-3-319-89960-2_21">10.1007/978-3-319-89960-2_21</a>'
  apa: 'Brázdil, T., Chatterjee, K., Kretinsky, J., &#38; Toman, V. (2018). Strategy
    representation by decision trees in reactive synthesis (Vol. 10805, pp. 385–407).
    Presented at the TACAS 2018: Tools and Algorithms for the Construction and Analysis
    of Systems, Thessaloniki, Greece: Springer. <a href="https://doi.org/10.1007/978-3-319-89960-2_21">https://doi.org/10.1007/978-3-319-89960-2_21</a>'
  chicago: Brázdil, Tomáš, Krishnendu Chatterjee, Jan Kretinsky, and Viktor Toman.
    “Strategy Representation by Decision Trees in Reactive Synthesis,” 10805:385–407.
    Springer, 2018. <a href="https://doi.org/10.1007/978-3-319-89960-2_21">https://doi.org/10.1007/978-3-319-89960-2_21</a>.
  ieee: 'T. Brázdil, K. Chatterjee, J. Kretinsky, and V. Toman, “Strategy representation
    by decision trees in reactive synthesis,” presented at the TACAS 2018: Tools and
    Algorithms for the Construction and Analysis of Systems, Thessaloniki, Greece,
    2018, vol. 10805, pp. 385–407.'
  ista: 'Brázdil T, Chatterjee K, Kretinsky J, Toman V. 2018. Strategy representation
    by decision trees in reactive synthesis. TACAS 2018: Tools and Algorithms for
    the Construction and Analysis of Systems, LNCS, vol. 10805, 385–407.'
  mla: Brázdil, Tomáš, et al. <i>Strategy Representation by Decision Trees in Reactive
    Synthesis</i>. Vol. 10805, Springer, 2018, pp. 385–407, doi:<a href="https://doi.org/10.1007/978-3-319-89960-2_21">10.1007/978-3-319-89960-2_21</a>.
  short: T. Brázdil, K. Chatterjee, J. Kretinsky, V. Toman, in:, Springer, 2018, pp.
    385–407.
conference:
  end_date: 2018-04-20
  location: Thessaloniki, Greece
  name: 'TACAS 2018: Tools and Algorithms for the Construction and Analysis of Systems'
  start_date: 2018-04-14
date_created: 2018-12-11T11:45:41Z
date_published: 2018-04-12T00:00:00Z
date_updated: 2025-06-02T08:53:40Z
day: '12'
ddc:
- '000'
department:
- _id: KrCh
- _id: ToHe
doi: 10.1007/978-3-319-89960-2_21
ec_funded: 1
external_id:
  isi:
  - '000546326300021'
file:
- access_level: open_access
  checksum: b13874ffb114932ad9cc2586b7469db4
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T16:29:08Z
  date_updated: 2020-07-14T12:45:57Z
  file_id: '5723'
  file_name: 2018_LNCS_Brazdil.pdf
  file_size: 1829940
  relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: '     10805'
isi: 1
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 385 - 407
project:
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
  grant_number: ICT15-003
  name: Efficient Algorithms for Computer Aided Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_status: published
publisher: Springer
publist_id: '7584'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Strategy representation by decision trees in reactive synthesis
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 10805
year: '2018'
...
