dHICA: a deep transformer-based model enables accurate histone imputation from chromatin accessibility.
- Publisher:
- OXFORD UNIV PRESS
- Publication Type:
- Journal Article
- Citation:
- Brief Bioinform, 2024, 25, (6), pp. bbae459
- Issue Date:
- 2024-09-23
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Wen, W | |
dc.contributor.author | Zhong, J | |
dc.contributor.author |
Zhang, Z https://orcid.org/0000-0002-3813-2776 |
|
dc.contributor.author | Jia, L | |
dc.contributor.author | Chu, T | |
dc.contributor.author | Wang, N | |
dc.contributor.author | Danko, CG | |
dc.contributor.author | Wang, Z | |
dc.date.accessioned | 2025-01-21T00:26:12Z | |
dc.date.available | 2024-09-04 | |
dc.date.available | 2025-01-21T00:26:12Z | |
dc.date.issued | 2024-09-23 | |
dc.identifier.citation | Brief Bioinform, 2024, 25, (6), pp. bbae459 | |
dc.identifier.issn | 1467-5463 | |
dc.identifier.issn | 1477-4054 | |
dc.identifier.uri | http://hdl.handle.net/10453/183895 | |
dc.description.abstract | Histone modifications (HMs) are pivotal in various biological processes, including transcription, replication, and DNA repair, significantly impacting chromatin structure. These modifications underpin the molecular mechanisms of cell-type-specific gene expression and complex diseases. However, annotating HMs across different cell types solely using experimental approaches is impractical due to cost and time constraints. Herein, we present dHICA (deep histone imputation using chromatin accessibility), a novel deep learning framework that integrates DNA sequences and chromatin accessibility data to predict multiple HM tracks. Employing the transformer architecture alongside dilated convolutions, dHICA boasts an extensive receptive field and captures more cell-type-specific information. dHICA outperforms state-of-the-art baselines and achieves superior performance in cell-type-specific loci and gene elements, aligning with biological expectations. Furthermore, dHICA's imputations hold significant potential for downstream applications, including chromatin state segmentation and elucidating the functional implications of SNPs (Single Nucleotide Polymorphisms). In conclusion, dHICA serves as a valuable tool for advancing the understanding of chromatin dynamics, offering enhanced predictive capabilities and interpretability. | |
dc.format | ||
dc.language | eng | |
dc.publisher | OXFORD UNIV PRESS | |
dc.relation.ispartof | Brief Bioinform | |
dc.relation.isbasedon | 10.1093/bib/bbae459 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 0601 Biochemistry and Cell Biology, 0802 Computation Theory and Mathematics, 0899 Other Information and Computing Sciences | |
dc.subject.classification | Bioinformatics | |
dc.subject.classification | 3101 Biochemistry and cell biology | |
dc.subject.classification | 3102 Bioinformatics and computational biology | |
dc.subject.classification | 3105 Genetics | |
dc.subject.mesh | Chromatin | |
dc.subject.mesh | Histones | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Polymorphism, Single Nucleotide | |
dc.subject.mesh | Deep Learning | |
dc.subject.mesh | Computational Biology | |
dc.subject.mesh | Histone Code | |
dc.subject.mesh | Chromatin | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Histones | |
dc.subject.mesh | Computational Biology | |
dc.subject.mesh | Histone Code | |
dc.subject.mesh | Polymorphism, Single Nucleotide | |
dc.subject.mesh | Deep Learning | |
dc.subject.mesh | Chromatin | |
dc.subject.mesh | Histones | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Polymorphism, Single Nucleotide | |
dc.subject.mesh | Deep Learning | |
dc.subject.mesh | Computational Biology | |
dc.subject.mesh | Histone Code | |
dc.title | dHICA: a deep transformer-based model enables accurate histone imputation from chromatin accessibility. | |
dc.type | Journal Article | |
utslib.citation.volume | 25 | |
utslib.location.activity | England | |
utslib.for | 0601 Biochemistry and Cell Biology | |
utslib.for | 0802 Computation Theory and Mathematics | |
utslib.for | 0899 Other Information and Computing Sciences | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology/School of Computer Science | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ | |
dc.date.updated | 2025-01-21T00:26:09Z | |
pubs.issue | 6 | |
pubs.publication-status | Published | |
pubs.volume | 25 | |
utslib.citation.issue | 6 |
Abstract:
Histone modifications (HMs) are pivotal in various biological processes, including transcription, replication, and DNA repair, significantly impacting chromatin structure. These modifications underpin the molecular mechanisms of cell-type-specific gene expression and complex diseases. However, annotating HMs across different cell types solely using experimental approaches is impractical due to cost and time constraints. Herein, we present dHICA (deep histone imputation using chromatin accessibility), a novel deep learning framework that integrates DNA sequences and chromatin accessibility data to predict multiple HM tracks. Employing the transformer architecture alongside dilated convolutions, dHICA boasts an extensive receptive field and captures more cell-type-specific information. dHICA outperforms state-of-the-art baselines and achieves superior performance in cell-type-specific loci and gene elements, aligning with biological expectations. Furthermore, dHICA's imputations hold significant potential for downstream applications, including chromatin state segmentation and elucidating the functional implications of SNPs (Single Nucleotide Polymorphisms). In conclusion, dHICA serves as a valuable tool for advancing the understanding of chromatin dynamics, offering enhanced predictive capabilities and interpretability.
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