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HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases

The chromatin interaction assays, particularly Hi-C, enable detailed studies of genome architecture in multiple organisms and model systems, resulting in a deeper understanding of gene expression regulation mechanisms mediated by epigenetics. However, the analysis and interpretation of Hi-C data rem...

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Autores principales: Kobets, Victoria A, Ulianov, Sergey V, Galitsyna, Aleksandra A, Doronin, Semen A, Mikhaleva, Elena A, Gelfand, Mikhail S, Shevelyov, Yuri Y, Razin, Sergey V, Khrameeva, Ekaterina E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025441/
https://www.ncbi.nlm.nih.gov/pubmed/36759336
http://dx.doi.org/10.1093/bib/bbad044
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author Kobets, Victoria A
Ulianov, Sergey V
Galitsyna, Aleksandra A
Doronin, Semen A
Mikhaleva, Elena A
Gelfand, Mikhail S
Shevelyov, Yuri Y
Razin, Sergey V
Khrameeva, Ekaterina E
author_facet Kobets, Victoria A
Ulianov, Sergey V
Galitsyna, Aleksandra A
Doronin, Semen A
Mikhaleva, Elena A
Gelfand, Mikhail S
Shevelyov, Yuri Y
Razin, Sergey V
Khrameeva, Ekaterina E
author_sort Kobets, Victoria A
collection PubMed
description The chromatin interaction assays, particularly Hi-C, enable detailed studies of genome architecture in multiple organisms and model systems, resulting in a deeper understanding of gene expression regulation mechanisms mediated by epigenetics. However, the analysis and interpretation of Hi-C data remain challenging due to technical biases, limiting direct comparisons of datasets obtained in different experiments and laboratories. As a result, removing biases from Hi-C-generated chromatin contact matrices is a critical data analysis step. Our novel approach, HiConfidence, eliminates biases from the Hi-C data by weighing chromatin contacts according to their consistency between replicates so that low-quality replicates do not substantially influence the result. The algorithm is effective for the analysis of global changes in chromatin structures such as compartments and topologically associating domains. We apply the HiConfidence approach to several Hi-C datasets with significant technical biases, that could not be analyzed effectively using existing methods, and obtain meaningful biological conclusions. In particular, HiConfidence aids in the study of how changes in histone acetylation pattern affect chromatin organization in Drosophila melanogaster S2 cells. The method is freely available at GitHub: https://github.com/victorykobets/HiConfidence.
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spelling pubmed-100254412023-03-21 HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases Kobets, Victoria A Ulianov, Sergey V Galitsyna, Aleksandra A Doronin, Semen A Mikhaleva, Elena A Gelfand, Mikhail S Shevelyov, Yuri Y Razin, Sergey V Khrameeva, Ekaterina E Brief Bioinform Problem Solving Protocol The chromatin interaction assays, particularly Hi-C, enable detailed studies of genome architecture in multiple organisms and model systems, resulting in a deeper understanding of gene expression regulation mechanisms mediated by epigenetics. However, the analysis and interpretation of Hi-C data remain challenging due to technical biases, limiting direct comparisons of datasets obtained in different experiments and laboratories. As a result, removing biases from Hi-C-generated chromatin contact matrices is a critical data analysis step. Our novel approach, HiConfidence, eliminates biases from the Hi-C data by weighing chromatin contacts according to their consistency between replicates so that low-quality replicates do not substantially influence the result. The algorithm is effective for the analysis of global changes in chromatin structures such as compartments and topologically associating domains. We apply the HiConfidence approach to several Hi-C datasets with significant technical biases, that could not be analyzed effectively using existing methods, and obtain meaningful biological conclusions. In particular, HiConfidence aids in the study of how changes in histone acetylation pattern affect chromatin organization in Drosophila melanogaster S2 cells. The method is freely available at GitHub: https://github.com/victorykobets/HiConfidence. Oxford University Press 2023-02-09 /pmc/articles/PMC10025441/ /pubmed/36759336 http://dx.doi.org/10.1093/bib/bbad044 Text en © The Author(s) 2023. Published by Oxford University Press. https://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 (https://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 Problem Solving Protocol
Kobets, Victoria A
Ulianov, Sergey V
Galitsyna, Aleksandra A
Doronin, Semen A
Mikhaleva, Elena A
Gelfand, Mikhail S
Shevelyov, Yuri Y
Razin, Sergey V
Khrameeva, Ekaterina E
HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases
title HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases
title_full HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases
title_fullStr HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases
title_full_unstemmed HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases
title_short HiConfidence: a novel approach uncovering the biological signal in Hi-C data affected by technical biases
title_sort hiconfidence: a novel approach uncovering the biological signal in hi-c data affected by technical biases
topic Problem Solving Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025441/
https://www.ncbi.nlm.nih.gov/pubmed/36759336
http://dx.doi.org/10.1093/bib/bbad044
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