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Effective normalization for copy number variation in Hi-C data

BACKGROUND: Normalization is essential to ensure accurate analysis and proper interpretation of sequencing data, and chromosome conformation capture data such as Hi-C have particular challenges. Although several methods have been proposed, the most widely used type of normalization of Hi-C data usua...

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Autores principales: Servant, Nicolas, Varoquaux, Nelle, Heard, Edith, Barillot, Emmanuel, Vert, Jean-Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127909/
https://www.ncbi.nlm.nih.gov/pubmed/30189838
http://dx.doi.org/10.1186/s12859-018-2256-5
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author Servant, Nicolas
Varoquaux, Nelle
Heard, Edith
Barillot, Emmanuel
Vert, Jean-Philippe
author_facet Servant, Nicolas
Varoquaux, Nelle
Heard, Edith
Barillot, Emmanuel
Vert, Jean-Philippe
author_sort Servant, Nicolas
collection PubMed
description BACKGROUND: Normalization is essential to ensure accurate analysis and proper interpretation of sequencing data, and chromosome conformation capture data such as Hi-C have particular challenges. Although several methods have been proposed, the most widely used type of normalization of Hi-C data usually casts estimation of unwanted effects as a matrix balancing problem, relying on the assumption that all genomic regions interact equally with each other. RESULTS: In order to explore the effect of copy-number variations on Hi-C data normalization, we first propose a simulation model that predict the effects of large copy-number changes on a diploid Hi-C contact map. We then show that the standard approaches relying on equal visibility fail to correct for unwanted effects in the presence of copy-number variations. We thus propose a simple extension to matrix balancing methods that model these effects. Our approach can either retain the copy-number variation effects (LOIC) or remove them (CAIC). We show that this leads to better downstream analysis of the three-dimensional organization of rearranged genomes. CONCLUSIONS: Taken together, our results highlight the importance of using dedicated methods for the analysis of Hi-C cancer data. Both CAIC and LOIC methods perform well on simulated and real Hi-C data sets, each fulfilling different needs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2256-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-61279092018-09-10 Effective normalization for copy number variation in Hi-C data Servant, Nicolas Varoquaux, Nelle Heard, Edith Barillot, Emmanuel Vert, Jean-Philippe BMC Bioinformatics Methodology Article BACKGROUND: Normalization is essential to ensure accurate analysis and proper interpretation of sequencing data, and chromosome conformation capture data such as Hi-C have particular challenges. Although several methods have been proposed, the most widely used type of normalization of Hi-C data usually casts estimation of unwanted effects as a matrix balancing problem, relying on the assumption that all genomic regions interact equally with each other. RESULTS: In order to explore the effect of copy-number variations on Hi-C data normalization, we first propose a simulation model that predict the effects of large copy-number changes on a diploid Hi-C contact map. We then show that the standard approaches relying on equal visibility fail to correct for unwanted effects in the presence of copy-number variations. We thus propose a simple extension to matrix balancing methods that model these effects. Our approach can either retain the copy-number variation effects (LOIC) or remove them (CAIC). We show that this leads to better downstream analysis of the three-dimensional organization of rearranged genomes. CONCLUSIONS: Taken together, our results highlight the importance of using dedicated methods for the analysis of Hi-C cancer data. Both CAIC and LOIC methods perform well on simulated and real Hi-C data sets, each fulfilling different needs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2256-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-06 /pmc/articles/PMC6127909/ /pubmed/30189838 http://dx.doi.org/10.1186/s12859-018-2256-5 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Methodology Article
Servant, Nicolas
Varoquaux, Nelle
Heard, Edith
Barillot, Emmanuel
Vert, Jean-Philippe
Effective normalization for copy number variation in Hi-C data
title Effective normalization for copy number variation in Hi-C data
title_full Effective normalization for copy number variation in Hi-C data
title_fullStr Effective normalization for copy number variation in Hi-C data
title_full_unstemmed Effective normalization for copy number variation in Hi-C data
title_short Effective normalization for copy number variation in Hi-C data
title_sort effective normalization for copy number variation in hi-c data
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127909/
https://www.ncbi.nlm.nih.gov/pubmed/30189838
http://dx.doi.org/10.1186/s12859-018-2256-5
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