» Articles » PMID: 31199868

HMMRATAC: a Hidden Markov ModeleR for ATAC-seq

Overview
Specialty Biochemistry
Date 2019 Jun 15
PMID 31199868
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

ATAC-seq has been widely adopted to identify accessible chromatin regions across the genome. However, current data analysis still utilizes approaches initially designed for ChIP-seq or DNase-seq, without considering the transposase digested DNA fragments that contain additional nucleosome positioning information. We present the first dedicated ATAC-seq analysis tool, a semi-supervised machine learning approach named HMMRATAC. HMMRATAC splits a single ATAC-seq dataset into nucleosome-free and nucleosome-enriched signals, learns the unique chromatin structure around accessible regions, and then predicts accessible regions across the entire genome. We show that HMMRATAC outperforms the popular peak-calling algorithms on published human ATAC-seq datasets. We find that single-end sequenced or size-selected ATAC-seq datasets result in a loss of sensitivity compared to paired-end datasets without size-selection.

Citing Articles

Genetic coupling of enhancer activity and connectivity in gene expression control.

Ray-Jones H, Sung C, Chan L, Haglund A, Artemov P, Della Rosa M Nat Commun. 2025; 16(1):970.

PMID: 39870618 PMC: 11772589. DOI: 10.1038/s41467-025-55900-3.


Heterochromatic gene silencing controls CD4 T cell susceptibility to regulatory T cell-mediated suppression in a murine allograft model.

Noguerol J, Laviolette K, Zahm M, Chaubet A, Sahal A, Detraves C Nat Commun. 2025; 16(1):566.

PMID: 39794349 PMC: 11723947. DOI: 10.1038/s41467-025-55848-4.


From Omics to Multi-Omics: A Review of Advantages and Tradeoffs.

Hayes C, Nakahara H, Ono A, Tsuge M, Oka S Genes (Basel). 2025; 15(12.

PMID: 39766818 PMC: 11675490. DOI: 10.3390/genes15121551.


Integrative multiomics reveals common endotypes across PSEN1, PSEN2, and APP mutations in familial Alzheimer's disease.

Valdes P, Caldwell A, Liu Q, Fitzgerald M, Ramachandran S, Karch C Alzheimers Res Ther. 2025; 17(1):5.

PMID: 39754192 PMC: 11699654. DOI: 10.1186/s13195-024-01659-6.


Review and Evaluate the Bioinformatics Analysis Strategies of ATAC-seq and CUT&Tag Data.

Cheng S, Miao B, Li T, Zhao G, Zhang B Genomics Proteomics Bioinformatics. 2024; 22(3).

PMID: 39255248 PMC: 11464419. DOI: 10.1093/gpbjnl/qzae054.


References
1.
Koohy H, Down T, Spivakov M, Hubbard T . A comparison of peak callers used for DNase-Seq data. PLoS One. 2014; 9(5):e96303. PMC: 4014496. DOI: 10.1371/journal.pone.0096303. View

2.
Li H, Durbin R . Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009; 25(14):1754-60. PMC: 2705234. DOI: 10.1093/bioinformatics/btp324. View

3.
Wang J, Quach B, Furey T . Correcting nucleotide-specific biases in high-throughput sequencing data. BMC Bioinformatics. 2017; 18(1):357. PMC: 5540620. DOI: 10.1186/s12859-017-1766-x. View

4.
Denny S, Yang D, Chuang C, Brady J, Lim J, Gruner B . Nfib Promotes Metastasis through a Widespread Increase in Chromatin Accessibility. Cell. 2016; 166(2):328-342. PMC: 5004630. DOI: 10.1016/j.cell.2016.05.052. View

5.
Kodama Y, Shumway M, Leinonen R . The Sequence Read Archive: explosive growth of sequencing data. Nucleic Acids Res. 2011; 40(Database issue):D54-6. PMC: 3245110. DOI: 10.1093/nar/gkr854. View