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A framework for group-wise summarization and comparison of chromatin state annotations
MOTIVATION: Genome-wide maps of epigenetic modifications are powerful resources for non-coding genome annotation. Maps of multiple epigenetics marks have been integrated into cell or tissue type-specific chromatin state annotations for many cell or tissue types. With the increasing availability of m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805555/ https://www.ncbi.nlm.nih.gov/pubmed/36342196 http://dx.doi.org/10.1093/bioinformatics/btac722 |
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author | Vu, Ha Koch, Zane Fiziev, Petko Ernst, Jason |
author_facet | Vu, Ha Koch, Zane Fiziev, Petko Ernst, Jason |
author_sort | Vu, Ha |
collection | PubMed |
description | MOTIVATION: Genome-wide maps of epigenetic modifications are powerful resources for non-coding genome annotation. Maps of multiple epigenetics marks have been integrated into cell or tissue type-specific chromatin state annotations for many cell or tissue types. With the increasing availability of multiple chromatin state maps for biologically similar samples, there is a need for methods that can effectively summarize the information about chromatin state annotations within groups of samples and identify differences across groups of samples at a high resolution. RESULTS: We developed CSREP, which takes as input chromatin state annotations for a group of samples. CSREP then probabilistically estimates the state at each genomic position and derives a representative chromatin state map for the group. CSREP uses an ensemble of multi-class logistic regression classifiers that predict the chromatin state assignment of each sample given the state maps from all other samples. The difference in CSREP’s probability assignments for the two groups can be used to identify genomic locations with differential chromatin state assignments. Using groups of chromatin state maps of a diverse set of cell and tissue types, we demonstrate the advantages of using CSREP to summarize chromatin state maps and identify biologically relevant differences between groups at a high resolution. AVAILABILITY AND IMPLEMENTATION: The CSREP source code and generated data are available at http://github.com/ernstlab/csrep. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-9805555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98055552023-01-03 A framework for group-wise summarization and comparison of chromatin state annotations Vu, Ha Koch, Zane Fiziev, Petko Ernst, Jason Bioinformatics Original Paper MOTIVATION: Genome-wide maps of epigenetic modifications are powerful resources for non-coding genome annotation. Maps of multiple epigenetics marks have been integrated into cell or tissue type-specific chromatin state annotations for many cell or tissue types. With the increasing availability of multiple chromatin state maps for biologically similar samples, there is a need for methods that can effectively summarize the information about chromatin state annotations within groups of samples and identify differences across groups of samples at a high resolution. RESULTS: We developed CSREP, which takes as input chromatin state annotations for a group of samples. CSREP then probabilistically estimates the state at each genomic position and derives a representative chromatin state map for the group. CSREP uses an ensemble of multi-class logistic regression classifiers that predict the chromatin state assignment of each sample given the state maps from all other samples. The difference in CSREP’s probability assignments for the two groups can be used to identify genomic locations with differential chromatin state assignments. Using groups of chromatin state maps of a diverse set of cell and tissue types, we demonstrate the advantages of using CSREP to summarize chromatin state maps and identify biologically relevant differences between groups at a high resolution. AVAILABILITY AND IMPLEMENTATION: The CSREP source code and generated data are available at http://github.com/ernstlab/csrep. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-11-07 /pmc/articles/PMC9805555/ /pubmed/36342196 http://dx.doi.org/10.1093/bioinformatics/btac722 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Vu, Ha Koch, Zane Fiziev, Petko Ernst, Jason A framework for group-wise summarization and comparison of chromatin state annotations |
title | A framework for group-wise summarization and comparison of chromatin state annotations |
title_full | A framework for group-wise summarization and comparison of chromatin state annotations |
title_fullStr | A framework for group-wise summarization and comparison of chromatin state annotations |
title_full_unstemmed | A framework for group-wise summarization and comparison of chromatin state annotations |
title_short | A framework for group-wise summarization and comparison of chromatin state annotations |
title_sort | framework for group-wise summarization and comparison of chromatin state annotations |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805555/ https://www.ncbi.nlm.nih.gov/pubmed/36342196 http://dx.doi.org/10.1093/bioinformatics/btac722 |
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