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HiDeF: identifying persistent structures in multiscale ‘omics data
In any ‘omics study, the scale of analysis can dramatically affect the outcome. For instance, when clustering single-cell transcriptomes, is the analysis tuned to discover broad or specific cell types? Likewise, protein communities revealed from protein networks can vary widely in sizes depending on...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789082/ https://www.ncbi.nlm.nih.gov/pubmed/33413539 http://dx.doi.org/10.1186/s13059-020-02228-4 |
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author | Zheng, Fan Zhang, She Churas, Christopher Pratt, Dexter Bahar, Ivet Ideker, Trey |
author_facet | Zheng, Fan Zhang, She Churas, Christopher Pratt, Dexter Bahar, Ivet Ideker, Trey |
author_sort | Zheng, Fan |
collection | PubMed |
description | In any ‘omics study, the scale of analysis can dramatically affect the outcome. For instance, when clustering single-cell transcriptomes, is the analysis tuned to discover broad or specific cell types? Likewise, protein communities revealed from protein networks can vary widely in sizes depending on the method. Here, we use the concept of persistent homology, drawn from mathematical topology, to identify robust structures in data at all scales simultaneously. Application to mouse single-cell transcriptomes significantly expands the catalog of identified cell types, while analysis of SARS-COV-2 protein interactions suggests hijacking of WNT. The method, HiDeF, is available via Python and Cytoscape. |
format | Online Article Text |
id | pubmed-7789082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77890822021-01-08 HiDeF: identifying persistent structures in multiscale ‘omics data Zheng, Fan Zhang, She Churas, Christopher Pratt, Dexter Bahar, Ivet Ideker, Trey Genome Biol Short Report In any ‘omics study, the scale of analysis can dramatically affect the outcome. For instance, when clustering single-cell transcriptomes, is the analysis tuned to discover broad or specific cell types? Likewise, protein communities revealed from protein networks can vary widely in sizes depending on the method. Here, we use the concept of persistent homology, drawn from mathematical topology, to identify robust structures in data at all scales simultaneously. Application to mouse single-cell transcriptomes significantly expands the catalog of identified cell types, while analysis of SARS-COV-2 protein interactions suggests hijacking of WNT. The method, HiDeF, is available via Python and Cytoscape. BioMed Central 2021-01-07 /pmc/articles/PMC7789082/ /pubmed/33413539 http://dx.doi.org/10.1186/s13059-020-02228-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Short Report Zheng, Fan Zhang, She Churas, Christopher Pratt, Dexter Bahar, Ivet Ideker, Trey HiDeF: identifying persistent structures in multiscale ‘omics data |
title | HiDeF: identifying persistent structures in multiscale ‘omics data |
title_full | HiDeF: identifying persistent structures in multiscale ‘omics data |
title_fullStr | HiDeF: identifying persistent structures in multiscale ‘omics data |
title_full_unstemmed | HiDeF: identifying persistent structures in multiscale ‘omics data |
title_short | HiDeF: identifying persistent structures in multiscale ‘omics data |
title_sort | hidef: identifying persistent structures in multiscale ‘omics data |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789082/ https://www.ncbi.nlm.nih.gov/pubmed/33413539 http://dx.doi.org/10.1186/s13059-020-02228-4 |
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