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OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes
The three-dimensional conformation of genomes is an essential component of their biological activity. The advent of the Hi-C technology enabled an unprecedented progress in our understanding of genome structures. However, Hi-C is subject to systematic biases that can compromise downstream analyses....
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/PMC5934634/ https://www.ncbi.nlm.nih.gov/pubmed/29394371 http://dx.doi.org/10.1093/nar/gky064 |
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author | Vidal, Enrique le Dily, François Quilez, Javier Stadhouders, Ralph Cuartero, Yasmina Graf, Thomas Marti-Renom, Marc A Beato, Miguel Filion, Guillaume J |
author_facet | Vidal, Enrique le Dily, François Quilez, Javier Stadhouders, Ralph Cuartero, Yasmina Graf, Thomas Marti-Renom, Marc A Beato, Miguel Filion, Guillaume J |
author_sort | Vidal, Enrique |
collection | PubMed |
description | The three-dimensional conformation of genomes is an essential component of their biological activity. The advent of the Hi-C technology enabled an unprecedented progress in our understanding of genome structures. However, Hi-C is subject to systematic biases that can compromise downstream analyses. Several strategies have been proposed to remove those biases, but the issue of abnormal karyotypes received little attention. Many experiments are performed in cancer cell lines, which typically harbor large-scale copy number variations that create visible defects on the raw Hi-C maps. The consequences of these widespread artifacts on the normalized maps are mostly unexplored. We observed that current normalization methods are not robust to the presence of large-scale copy number variations, potentially obscuring biological differences and enhancing batch effects. To address this issue, we developed an alternative approach designed to take into account chromosomal abnormalities. The method, called OneD, increases reproducibility among replicates of Hi-C samples with abnormal karyotype, outperforming previous methods significantly. On normal karyotypes, OneD fared equally well as state-of-the-art methods, making it a safe choice for Hi-C normalization. OneD is fast and scales well in terms of computing resources for resolutions up to 5 kb. |
format | Online Article Text |
id | pubmed-5934634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59346342018-05-09 OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes Vidal, Enrique le Dily, François Quilez, Javier Stadhouders, Ralph Cuartero, Yasmina Graf, Thomas Marti-Renom, Marc A Beato, Miguel Filion, Guillaume J Nucleic Acids Res Methods Online The three-dimensional conformation of genomes is an essential component of their biological activity. The advent of the Hi-C technology enabled an unprecedented progress in our understanding of genome structures. However, Hi-C is subject to systematic biases that can compromise downstream analyses. Several strategies have been proposed to remove those biases, but the issue of abnormal karyotypes received little attention. Many experiments are performed in cancer cell lines, which typically harbor large-scale copy number variations that create visible defects on the raw Hi-C maps. The consequences of these widespread artifacts on the normalized maps are mostly unexplored. We observed that current normalization methods are not robust to the presence of large-scale copy number variations, potentially obscuring biological differences and enhancing batch effects. To address this issue, we developed an alternative approach designed to take into account chromosomal abnormalities. The method, called OneD, increases reproducibility among replicates of Hi-C samples with abnormal karyotype, outperforming previous methods significantly. On normal karyotypes, OneD fared equally well as state-of-the-art methods, making it a safe choice for Hi-C normalization. OneD is fast and scales well in terms of computing resources for resolutions up to 5 kb. Oxford University Press 2018-05-04 2018-01-31 /pmc/articles/PMC5934634/ /pubmed/29394371 http://dx.doi.org/10.1093/nar/gky064 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Vidal, Enrique le Dily, François Quilez, Javier Stadhouders, Ralph Cuartero, Yasmina Graf, Thomas Marti-Renom, Marc A Beato, Miguel Filion, Guillaume J OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes |
title | OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes |
title_full | OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes |
title_fullStr | OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes |
title_full_unstemmed | OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes |
title_short | OneD: increasing reproducibility of Hi-C samples with abnormal karyotypes |
title_sort | oned: increasing reproducibility of hi-c samples with abnormal karyotypes |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934634/ https://www.ncbi.nlm.nih.gov/pubmed/29394371 http://dx.doi.org/10.1093/nar/gky064 |
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