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SnapFISH: a computational pipeline to identify chromatin loops from multiplexed DNA FISH data
Multiplexed DNA fluorescence in situ hybridization (FISH) imaging technologies have been developed to map the folding of chromatin fibers at tens of nanometers and up to several kilobases in resolution in single cells. However, computational methods to reliably identify chromatin loops from such ima...
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Published in: | Nature communications 2023-08, Vol.14 (1), p.4873-7, Article 4873 |
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creator | Lee, Lindsay Yu, Hongyu Jia, Bojing Blair Jussila, Adam Zhu, Chenxu Chen, Jiawen Xie, Liangqi Hafner, Antonina Mishra, Shreya Wang, Duan Dennis Strambio-De-Castillia, Caterina Boettiger, Alistair Ren, Bing Li, Yun Hu, Ming |
description | Multiplexed DNA fluorescence in situ hybridization (FISH) imaging technologies have been developed to map the folding of chromatin fibers at tens of nanometers and up to several kilobases in resolution in single cells. However, computational methods to reliably identify chromatin loops from such imaging datasets are still lacking. Here we present a Single-Nucleus Analysis Pipeline for multiplexed DNA FISH (SnapFISH), to process the multiplexed DNA FISH data and identify chromatin loops. SnapFISH can identify known chromatin loops from mouse embryonic stem cells with high sensitivity and accuracy. In addition, SnapFISH obtains comparable results of chromatin loops across datasets generated from diverse imaging technologies. SnapFISH is freely available at
https://github.com/HuMingLab/SnapFISH
.
Multiplexed DNA FISH technologies are powerful tools to reveal chromatin spatial organisation. Here, the authors developed SnapFISH, a computational pipeline to identify chromatin loops from multiplexed DNA FISH data. |
doi_str_mv | 10.1038/s41467-023-40658-3 |
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https://github.com/HuMingLab/SnapFISH
.
Multiplexed DNA FISH technologies are powerful tools to reveal chromatin spatial organisation. Here, the authors developed SnapFISH, a computational pipeline to identify chromatin loops from multiplexed DNA FISH data.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/s41467-023-40658-3</identifier><identifier>PMID: 37573342</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45 ; 631/114/2415 ; 631/114/794 ; 631/1647/1513 ; 631/1647/48 ; 631/61/212/177 ; Animals ; Biology ; Candidates ; Chromatin ; Chromatin - genetics ; Computer applications ; Datasets ; Deoxyribonucleic acid ; DNA ; DNA - genetics ; Embryo cells ; Fibers ; Fluorescence in situ hybridization ; Genomes ; Humanities and Social Sciences ; Imaging ; In Situ Hybridization, Fluorescence - methods ; Localization ; Medical research ; Mice ; multidisciplinary ; Multiplexing ; Neighborhoods ; Research centers ; Science ; Science (multidisciplinary) ; Stem cells</subject><ispartof>Nature communications, 2023-08, Vol.14 (1), p.4873-7, Article 4873</ispartof><rights>The Author(s) 2023</rights><rights>2023. Springer Nature Limited.</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Springer Nature Limited 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-d8d47746340f6e85556455179c1ffa0447a71d264bfe05d7fd45577cdbefa7d73</citedby><cites>FETCH-LOGICAL-c541t-d8d47746340f6e85556455179c1ffa0447a71d264bfe05d7fd45577cdbefa7d73</cites><orcidid>0000-0003-4216-6562 ; 0000-0002-1069-1816 ; 0000-0002-9275-4189 ; 0000-0003-0987-2916</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2849396821/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2849396821?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37573342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Lindsay</creatorcontrib><creatorcontrib>Yu, Hongyu</creatorcontrib><creatorcontrib>Jia, Bojing Blair</creatorcontrib><creatorcontrib>Jussila, Adam</creatorcontrib><creatorcontrib>Zhu, Chenxu</creatorcontrib><creatorcontrib>Chen, Jiawen</creatorcontrib><creatorcontrib>Xie, Liangqi</creatorcontrib><creatorcontrib>Hafner, Antonina</creatorcontrib><creatorcontrib>Mishra, Shreya</creatorcontrib><creatorcontrib>Wang, Duan Dennis</creatorcontrib><creatorcontrib>Strambio-De-Castillia, Caterina</creatorcontrib><creatorcontrib>Boettiger, Alistair</creatorcontrib><creatorcontrib>Ren, Bing</creatorcontrib><creatorcontrib>Li, Yun</creatorcontrib><creatorcontrib>Hu, Ming</creatorcontrib><title>SnapFISH: a computational pipeline to identify chromatin loops from multiplexed DNA FISH data</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>Multiplexed DNA fluorescence in situ hybridization (FISH) imaging technologies have been developed to map the folding of chromatin fibers at tens of nanometers and up to several kilobases in resolution in single cells. However, computational methods to reliably identify chromatin loops from such imaging datasets are still lacking. Here we present a Single-Nucleus Analysis Pipeline for multiplexed DNA FISH (SnapFISH), to process the multiplexed DNA FISH data and identify chromatin loops. SnapFISH can identify known chromatin loops from mouse embryonic stem cells with high sensitivity and accuracy. In addition, SnapFISH obtains comparable results of chromatin loops across datasets generated from diverse imaging technologies. SnapFISH is freely available at
https://github.com/HuMingLab/SnapFISH
.
Multiplexed DNA FISH technologies are powerful tools to reveal chromatin spatial organisation. 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Commun</addtitle><date>2023-08-12</date><risdate>2023</risdate><volume>14</volume><issue>1</issue><spage>4873</spage><epage>7</epage><pages>4873-7</pages><artnum>4873</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Multiplexed DNA fluorescence in situ hybridization (FISH) imaging technologies have been developed to map the folding of chromatin fibers at tens of nanometers and up to several kilobases in resolution in single cells. However, computational methods to reliably identify chromatin loops from such imaging datasets are still lacking. Here we present a Single-Nucleus Analysis Pipeline for multiplexed DNA FISH (SnapFISH), to process the multiplexed DNA FISH data and identify chromatin loops. SnapFISH can identify known chromatin loops from mouse embryonic stem cells with high sensitivity and accuracy. In addition, SnapFISH obtains comparable results of chromatin loops across datasets generated from diverse imaging technologies. SnapFISH is freely available at
https://github.com/HuMingLab/SnapFISH
.
Multiplexed DNA FISH technologies are powerful tools to reveal chromatin spatial organisation. Here, the authors developed SnapFISH, a computational pipeline to identify chromatin loops from multiplexed DNA FISH data.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>37573342</pmid><doi>10.1038/s41467-023-40658-3</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4216-6562</orcidid><orcidid>https://orcid.org/0000-0002-1069-1816</orcidid><orcidid>https://orcid.org/0000-0002-9275-4189</orcidid><orcidid>https://orcid.org/0000-0003-0987-2916</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 45 631/114/2415 631/114/794 631/1647/1513 631/1647/48 631/61/212/177 Animals Biology Candidates Chromatin Chromatin - genetics Computer applications Datasets Deoxyribonucleic acid DNA DNA - genetics Embryo cells Fibers Fluorescence in situ hybridization Genomes Humanities and Social Sciences Imaging In Situ Hybridization, Fluorescence - methods Localization Medical research Mice multidisciplinary Multiplexing Neighborhoods Research centers Science Science (multidisciplinary) Stem cells |
title | SnapFISH: a computational pipeline to identify chromatin loops from multiplexed DNA FISH data |
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