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peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data
It is becoming increasingly clear that chromosome organization plays an important role in gene regulation. High-resolution methods such as 4C, Capture-C and promoter capture Hi-C (PCHiC) enable the study of chromatin loops such as those formed between promoters and enhancers or CTCF/cohesin binding...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125690/ https://www.ncbi.nlm.nih.gov/pubmed/29800273 http://dx.doi.org/10.1093/nar/gky443 |
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author | Geeven, Geert Teunissen, Hans de Laat, Wouter de Wit, Elzo |
author_facet | Geeven, Geert Teunissen, Hans de Laat, Wouter de Wit, Elzo |
author_sort | Geeven, Geert |
collection | PubMed |
description | It is becoming increasingly clear that chromosome organization plays an important role in gene regulation. High-resolution methods such as 4C, Capture-C and promoter capture Hi-C (PCHiC) enable the study of chromatin loops such as those formed between promoters and enhancers or CTCF/cohesin binding sites. An important aspect of 4C/Capture-C/PCHiC analyses is the reliable identification of chromatin loops, preferably not based on visual inspection of a DNA contact profile, but on reproducible statistical analysis that robustly scores interaction peaks in the non-uniform contact background. Here, we present peakC, an R package for the analysis of 4C/Capture-C/PCHiC data. We generated 4C data for 13 viewpoints in two tissues in at least triplicate to test our methods. We developed a non-parametric peak caller based on rank-products. Sampling analysis shows that not read depth but template quality is the most important determinant of success in 4C experiments. By performing peak calling on single experiments we show that the peak calling results are similar to the replicate experiments, but that false positive rates are significantly reduced by performing replicates. Our software is user-friendly and enables robust peak calling for one-vs-all chromosome capture experiments. peakC is available at: https://github.com/deWitLab/peakC. |
format | Online Article Text |
id | pubmed-6125690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61256902018-09-11 peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data Geeven, Geert Teunissen, Hans de Laat, Wouter de Wit, Elzo Nucleic Acids Res Methods Online It is becoming increasingly clear that chromosome organization plays an important role in gene regulation. High-resolution methods such as 4C, Capture-C and promoter capture Hi-C (PCHiC) enable the study of chromatin loops such as those formed between promoters and enhancers or CTCF/cohesin binding sites. An important aspect of 4C/Capture-C/PCHiC analyses is the reliable identification of chromatin loops, preferably not based on visual inspection of a DNA contact profile, but on reproducible statistical analysis that robustly scores interaction peaks in the non-uniform contact background. Here, we present peakC, an R package for the analysis of 4C/Capture-C/PCHiC data. We generated 4C data for 13 viewpoints in two tissues in at least triplicate to test our methods. We developed a non-parametric peak caller based on rank-products. Sampling analysis shows that not read depth but template quality is the most important determinant of success in 4C experiments. By performing peak calling on single experiments we show that the peak calling results are similar to the replicate experiments, but that false positive rates are significantly reduced by performing replicates. Our software is user-friendly and enables robust peak calling for one-vs-all chromosome capture experiments. peakC is available at: https://github.com/deWitLab/peakC. Oxford University Press 2018-09-06 2018-05-25 /pmc/articles/PMC6125690/ /pubmed/29800273 http://dx.doi.org/10.1093/nar/gky443 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Geeven, Geert Teunissen, Hans de Laat, Wouter de Wit, Elzo peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data |
title | peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data |
title_full | peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data |
title_fullStr | peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data |
title_full_unstemmed | peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data |
title_short | peakC: a flexible, non-parametric peak calling package for 4C and Capture-C data |
title_sort | peakc: a flexible, non-parametric peak calling package for 4c and capture-c data |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125690/ https://www.ncbi.nlm.nih.gov/pubmed/29800273 http://dx.doi.org/10.1093/nar/gky443 |
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