---
_id: '8707'
abstract:
- lang: eng
  text: Dynamic changes in the three-dimensional (3D) organization of chromatin are
    associated with central biological processes, such as transcription, replication
    and development. Therefore, the comprehensive identification and quantification
    of these changes is fundamental to understanding of evolutionary and regulatory
    mechanisms. Here, we present Comparison of Hi-C Experiments using Structural Similarity
    (CHESS), an algorithm for the comparison of chromatin contact maps and automatic
    differential feature extraction. We demonstrate the robustness of CHESS to experimental
    variability and showcase its biological applications on (1) interspecies comparisons
    of syntenic regions in human and mouse models; (2) intraspecies identification
    of conformational changes in Zelda-depleted Drosophila embryos; (3) patient-specific
    aberrant chromatin conformation in a diffuse large B-cell lymphoma sample; and
    (4) the systematic identification of chromatin contact differences in high-resolution
    Capture-C data. In summary, CHESS is a computationally efficient method for the
    comparison and classification of changes in chromatin contact data.
acknowledgement: 'Work in the Vaquerizas laboratory is funded by the Max Planck Society,
  the Deutsche Forschungsgemeinschaft (DFG) Priority Programme SPP 2202 ‘Spatial Genome
  Architecture in Development and Disease’ (project no. 422857230 to J.M.V.), the
  DFG Clinical Research Unit CRU326 ‘Male Germ Cells: from Genes to Function’ (project
  no. 329621271 to J.M.V.), the European Union’s Horizon 2020 research and innovation
  programme under the Marie Skłodowska-Curie grant agreement no. 643062—ZENCODE-ITN
  to J.M.V.) and the Medical Research Council in the UK. This research was partially
  funded by the European Union’s H2020 Framework Programme through the European Research
  Council (grant no. 609989 to M.A.M.-R.). We thank the support of the Spanish Ministerio
  de Ciencia, Innovación y Universidades through grant no. BFU2017-85926-P to M.A.M.-R.
  The Centre for Genomic Regulation thanks the support of the Ministerio de Ciencia,
  Innovación y Universidades to the European Molecular Biology Laboratory partnership,
  the ‘Centro de Excelencia Severo Ochoa 2013–2017’, agreement no. SEV-2012-0208,
  the CERCA Programme/Generalitat de Catalunya, Spanish Ministerio de Ciencia, Innovación
  y Universidades through the Instituto de Salud Carlos III, the Generalitat de Catalunya
  through the Departament de Salut and Departament d’Empresa i Coneixement and cofinancing
  by the Spanish Ministerio de Ciencia, Innovación y Universidades with funds from
  the European Regional Development Fund corresponding to the 2014–2020 Smart Growth
  Operating Program. S.G. thanks the support from the Company of Biologists (grant
  no. JCSTF181158) and the European Molecular Biology Organization Short-Term Fellowship
  programme.'
article_processing_charge: No
article_type: original
author:
- first_name: Silvia
  full_name: ' Galan, Silvia'
  last_name: ' Galan'
- first_name: Nick N
  full_name: Machnik, Nick N
  id: 3591A0AA-F248-11E8-B48F-1D18A9856A87
  last_name: Machnik
  orcid: 0000-0001-6617-9742
- first_name: Kai
  full_name: Kruse, Kai
  last_name: Kruse
- first_name: Noelia
  full_name: Díaz, Noelia
  last_name: Díaz
- first_name: Marc A
  full_name: Marti-Renom, Marc A
  last_name: Marti-Renom
- first_name: Juan M
  full_name: Vaquerizas, Juan M
  last_name: Vaquerizas
citation:
  ama: Galan S, Machnik NN, Kruse K, Díaz N, Marti-Renom MA, Vaquerizas JM. CHESS
    enables quantitative comparison of chromatin contact data and automatic feature
    extraction. <i>Nature Genetics</i>. 2020;52:1247-1255. doi:<a href="https://doi.org/10.1038/s41588-020-00712-y">10.1038/s41588-020-00712-y</a>
  apa: Galan, S., Machnik, N. N., Kruse, K., Díaz, N., Marti-Renom, M. A., &#38; Vaquerizas,
    J. M. (2020). CHESS enables quantitative comparison of chromatin contact data
    and automatic feature extraction. <i>Nature Genetics</i>. Springer Nature. <a
    href="https://doi.org/10.1038/s41588-020-00712-y">https://doi.org/10.1038/s41588-020-00712-y</a>
  chicago: Galan, Silvia, Nick N Machnik, Kai Kruse, Noelia Díaz, Marc A Marti-Renom,
    and Juan M Vaquerizas. “CHESS Enables Quantitative Comparison of Chromatin Contact
    Data and Automatic Feature Extraction.” <i>Nature Genetics</i>. Springer Nature,
    2020. <a href="https://doi.org/10.1038/s41588-020-00712-y">https://doi.org/10.1038/s41588-020-00712-y</a>.
  ieee: S.  Galan, N. N. Machnik, K. Kruse, N. Díaz, M. A. Marti-Renom, and J. M.
    Vaquerizas, “CHESS enables quantitative comparison of chromatin contact data and
    automatic feature extraction,” <i>Nature Genetics</i>, vol. 52. Springer Nature,
    pp. 1247–1255, 2020.
  ista: Galan S, Machnik NN, Kruse K, Díaz N, Marti-Renom MA, Vaquerizas JM. 2020.
    CHESS enables quantitative comparison of chromatin contact data and automatic
    feature extraction. Nature Genetics. 52, 1247–1255.
  mla: Galan, Silvia, et al. “CHESS Enables Quantitative Comparison of Chromatin Contact
    Data and Automatic Feature Extraction.” <i>Nature Genetics</i>, vol. 52, Springer
    Nature, 2020, pp. 1247–55, doi:<a href="https://doi.org/10.1038/s41588-020-00712-y">10.1038/s41588-020-00712-y</a>.
  short: S.  Galan, N.N. Machnik, K. Kruse, N. Díaz, M.A. Marti-Renom, J.M. Vaquerizas,
    Nature Genetics 52 (2020) 1247–1255.
date_created: 2020-10-25T23:01:20Z
date_published: 2020-10-19T00:00:00Z
date_updated: 2023-08-22T10:37:10Z
day: '19'
department:
- _id: FyKo
doi: 10.1038/s41588-020-00712-y
external_id:
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  pmid:
  - '33077914'
intvolume: '        52'
isi: 1
language:
- iso: eng
month: '10'
oa_version: None
page: 1247-1255
pmid: 1
publication: Nature Genetics
publication_identifier:
  eissn:
  - '15461718'
  issn:
  - '10614036'
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: CHESS enables quantitative comparison of chromatin contact data and automatic
  feature extraction
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 52
year: '2020'
...
---
_id: '653'
abstract:
- lang: eng
  text: The extent of heterogeneity among driver gene mutations present in naturally
    occurring metastases - that is, treatment-naive metastatic disease - is largely
    unknown. To address this issue, we carried out 60× whole-genome sequencing of
    26 metastases from four patients with pancreatic cancer. We found that identical
    mutations in known driver genes were present in every metastatic lesion for each
    patient studied. Passenger gene mutations, which do not have known or predicted
    functional consequences, accounted for all intratumoral heterogeneity. Even with
    respect to these passenger mutations, our analysis suggests that the genetic similarity
    among the founding cells of metastases was higher than that expected for any two
    cells randomly taken from a normal tissue. The uniformity of known driver gene
    mutations among metastases in the same patient has critical and encouraging implications
    for the success of future targeted therapies in advanced-stage disease.
acknowledgement: 'We thank the Memorial Sloan Kettering Cancer Center Molecular Cytology
  core facility for immunohistochemistry staining. This work was supported by Office
  of Naval Research grant N00014-16-1-2914, the Bill and Melinda Gates Foundation
  (OPP1148627), and a gift from B. Wu and E. Larson (M.A.N.), National Institutes
  of Health grants CA179991 (C.A.I.-D. and I.B.), F31 CA180682 (A.P.M.-M.), CA43460
  (B.V.), and P50 CA62924, the Monastra Foundation, the Virginia and D.K. Ludwig Fund
  for Cancer Research, the Lustgarten Foundation for Pancreatic Cancer Research, the
  Sol Goldman Center for Pancreatic Cancer Research, the Sol Goldman Sequencing Center,
  ERC Start grant 279307: Graph Games (J.G.R., D.K., and C.K.), Austrian Science Fund
  (FWF) grant P23499-N23 (J.G.R., D.K., and C.K.), and FWF NFN grant S11407-N23 RiSE/SHiNE
  (J.G.R., D.K., and C.K.).'
article_processing_charge: No
article_type: original
author:
- first_name: Alvin
  full_name: Makohon Moore, Alvin
  last_name: Makohon Moore
- first_name: Ming
  full_name: Zhang, Ming
  last_name: Zhang
- first_name: Johannes
  full_name: Reiter, Johannes
  id: 4A918E98-F248-11E8-B48F-1D18A9856A87
  last_name: Reiter
  orcid: 0000-0002-0170-7353
- first_name: Ivana
  full_name: Božić, Ivana
  last_name: Božić
- first_name: Benjamin
  full_name: Allen, Benjamin
  last_name: Allen
- first_name: Deepanjan
  full_name: Kundu, Deepanjan
  id: 1d4c0f4f-e8a3-11ec-a351-e36772758c45
  last_name: Kundu
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Fay
  full_name: Wong, Fay
  last_name: Wong
- first_name: Yuchen
  full_name: Jiao, Yuchen
  last_name: Jiao
- first_name: Zachary
  full_name: Kohutek, Zachary
  last_name: Kohutek
- first_name: Jungeui
  full_name: Hong, Jungeui
  last_name: Hong
- first_name: Marc
  full_name: Attiyeh, Marc
  last_name: Attiyeh
- first_name: Breanna
  full_name: Javier, Breanna
  last_name: Javier
- first_name: Laura
  full_name: Wood, Laura
  last_name: Wood
- first_name: Ralph
  full_name: Hruban, Ralph
  last_name: Hruban
- first_name: Martin
  full_name: Nowak, Martin
  last_name: Nowak
- first_name: Nickolas
  full_name: Papadopoulos, Nickolas
  last_name: Papadopoulos
- first_name: Kenneth
  full_name: Kinzler, Kenneth
  last_name: Kinzler
- first_name: Bert
  full_name: Vogelstein, Bert
  last_name: Vogelstein
- first_name: Christine
  full_name: Iacobuzio Donahue, Christine
  last_name: Iacobuzio Donahue
citation:
  ama: Makohon Moore A, Zhang M, Reiter J, et al. Limited heterogeneity of known driver
    gene mutations among the metastases of individual patients with pancreatic cancer.
    <i>Nature Genetics</i>. 2017;49(3):358-366. doi:<a href="https://doi.org/10.1038/ng.3764">10.1038/ng.3764</a>
  apa: Makohon Moore, A., Zhang, M., Reiter, J., Božić, I., Allen, B., Kundu, D.,
    … Iacobuzio Donahue, C. (2017). Limited heterogeneity of known driver gene mutations
    among the metastases of individual patients with pancreatic cancer. <i>Nature
    Genetics</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/ng.3764">https://doi.org/10.1038/ng.3764</a>
  chicago: Makohon Moore, Alvin, Ming Zhang, Johannes Reiter, Ivana Božić, Benjamin
    Allen, Deepanjan Kundu, Krishnendu Chatterjee, et al. “Limited Heterogeneity of
    Known Driver Gene Mutations among the Metastases of Individual Patients with Pancreatic
    Cancer.” <i>Nature Genetics</i>. Nature Publishing Group, 2017. <a href="https://doi.org/10.1038/ng.3764">https://doi.org/10.1038/ng.3764</a>.
  ieee: A. Makohon Moore <i>et al.</i>, “Limited heterogeneity of known driver gene
    mutations among the metastases of individual patients with pancreatic cancer,”
    <i>Nature Genetics</i>, vol. 49, no. 3. Nature Publishing Group, pp. 358–366,
    2017.
  ista: Makohon Moore A, Zhang M, Reiter J, Božić I, Allen B, Kundu D, Chatterjee
    K, Wong F, Jiao Y, Kohutek Z, Hong J, Attiyeh M, Javier B, Wood L, Hruban R, Nowak
    M, Papadopoulos N, Kinzler K, Vogelstein B, Iacobuzio Donahue C. 2017. Limited
    heterogeneity of known driver gene mutations among the metastases of individual
    patients with pancreatic cancer. Nature Genetics. 49(3), 358–366.
  mla: Makohon Moore, Alvin, et al. “Limited Heterogeneity of Known Driver Gene Mutations
    among the Metastases of Individual Patients with Pancreatic Cancer.” <i>Nature
    Genetics</i>, vol. 49, no. 3, Nature Publishing Group, 2017, pp. 358–66, doi:<a
    href="https://doi.org/10.1038/ng.3764">10.1038/ng.3764</a>.
  short: A. Makohon Moore, M. Zhang, J. Reiter, I. Božić, B. Allen, D. Kundu, K. Chatterjee,
    F. Wong, Y. Jiao, Z. Kohutek, J. Hong, M. Attiyeh, B. Javier, L. Wood, R. Hruban,
    M. Nowak, N. Papadopoulos, K. Kinzler, B. Vogelstein, C. Iacobuzio Donahue, Nature
    Genetics 49 (2017) 358–366.
date_created: 2018-12-11T11:47:43Z
date_published: 2017-03-01T00:00:00Z
date_updated: 2022-06-10T09:55:08Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1038/ng.3764
ec_funded: 1
external_id:
  pmid:
  - '28092682'
file:
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language:
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oa_version: Submitted Version
page: 358 - 366
pmid: 1
project:
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11407
  name: Game Theory
publication: Nature Genetics
publication_identifier:
  issn:
  - '10614036'
publication_status: published
publisher: Nature Publishing Group
publist_id: '7092'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Limited heterogeneity of known driver gene mutations among the metastases of
  individual patients with pancreatic cancer
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 49
year: '2017'
...
