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ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data

MOTIVATION: Several computational and statistical methods have been developed to analyze data generated through the 3C-based methods, especially the Hi-C. Most of the existing methods do not account for dependency in Hi-C data. RESULTS: Here, we present ZipHiC, a novel statistical method to explore...

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Detalles Bibliográficos
Autores principales: Osuntoki, Itunu G, Harrison, Andrew, Dai, Hongsheng, Bao, Yanchun, Zabet, Nicolae Radu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272800/
https://www.ncbi.nlm.nih.gov/pubmed/35678507
http://dx.doi.org/10.1093/bioinformatics/btac387
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author Osuntoki, Itunu G
Harrison, Andrew
Dai, Hongsheng
Bao, Yanchun
Zabet, Nicolae Radu
author_facet Osuntoki, Itunu G
Harrison, Andrew
Dai, Hongsheng
Bao, Yanchun
Zabet, Nicolae Radu
author_sort Osuntoki, Itunu G
collection PubMed
description MOTIVATION: Several computational and statistical methods have been developed to analyze data generated through the 3C-based methods, especially the Hi-C. Most of the existing methods do not account for dependency in Hi-C data. RESULTS: Here, we present ZipHiC, a novel statistical method to explore Hi-C data focusing on the detection of enriched contacts. ZipHiC implements a Bayesian method based on a hidden Markov random field (HMRF) model and the Approximate Bayesian Computation (ABC) to detect interactions in two-dimensional space based on a Hi-C contact frequency matrix. ZipHiC uses data on the sources of biases related to the contact frequency matrix, allows borrowing information from neighbours using the Potts model and improves computation speed using the ABC model. In addition to outperforming existing tools on both simulated and real data, our model also provides insights into different sources of biases that affects Hi-C data. We show that some datasets display higher biases from DNA accessibility or Transposable Elements content. Furthermore, our analysis in Drosophila melanogaster showed that approximately half of the detected significant interactions connect promoters with other parts of the genome indicating a functional biological role. Finally, we found that the micro-C datasets display higher biases from DNA accessibility compared to a similar Hi-C experiment, but this can be corrected by ZipHiC. AVAILABILITY AND IMPLEMENTATION: The R scripts are available at https://github.com/igosungithub/HMRFHiC.git. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-92728002022-07-11 ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data Osuntoki, Itunu G Harrison, Andrew Dai, Hongsheng Bao, Yanchun Zabet, Nicolae Radu Bioinformatics Original Papers MOTIVATION: Several computational and statistical methods have been developed to analyze data generated through the 3C-based methods, especially the Hi-C. Most of the existing methods do not account for dependency in Hi-C data. RESULTS: Here, we present ZipHiC, a novel statistical method to explore Hi-C data focusing on the detection of enriched contacts. ZipHiC implements a Bayesian method based on a hidden Markov random field (HMRF) model and the Approximate Bayesian Computation (ABC) to detect interactions in two-dimensional space based on a Hi-C contact frequency matrix. ZipHiC uses data on the sources of biases related to the contact frequency matrix, allows borrowing information from neighbours using the Potts model and improves computation speed using the ABC model. In addition to outperforming existing tools on both simulated and real data, our model also provides insights into different sources of biases that affects Hi-C data. We show that some datasets display higher biases from DNA accessibility or Transposable Elements content. Furthermore, our analysis in Drosophila melanogaster showed that approximately half of the detected significant interactions connect promoters with other parts of the genome indicating a functional biological role. Finally, we found that the micro-C datasets display higher biases from DNA accessibility compared to a similar Hi-C experiment, but this can be corrected by ZipHiC. AVAILABILITY AND IMPLEMENTATION: The R scripts are available at https://github.com/igosungithub/HMRFHiC.git. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-06-09 /pmc/articles/PMC9272800/ /pubmed/35678507 http://dx.doi.org/10.1093/bioinformatics/btac387 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 Papers
Osuntoki, Itunu G
Harrison, Andrew
Dai, Hongsheng
Bao, Yanchun
Zabet, Nicolae Radu
ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data
title ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data
title_full ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data
title_fullStr ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data
title_full_unstemmed ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data
title_short ZipHiC: a novel Bayesian framework to identify enriched interactions and experimental biases in Hi-C data
title_sort ziphic: a novel bayesian framework to identify enriched interactions and experimental biases in hi-c data
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272800/
https://www.ncbi.nlm.nih.gov/pubmed/35678507
http://dx.doi.org/10.1093/bioinformatics/btac387
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