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ABSTRACT: Summary
Identification of functional transcriptional regulators associated with chromatin in-teractions is an important problem in studies of 3-dimensional genome organization and gene regulation. Direct inference of TR binding has been limited by the resolu-tion of Hi-C data. Here, we present BART3D, a computational method for inferring TRs associated with genome-wide differential chromatin interactions by comparing Hi-C maps from two states, leveraging public ChIP-seq data for human and mouse. We demonstrate that BART3D can detect relevant TRs from dynamic Hi-C profiles with TR perturbation or cell differentiation. BART3D can be a useful tool in 3D genome data analysis and functional genomics research.Availability and implementation
BART3D is implemented in Python and the source code is available at https://github.com/zanglab/bart3d.Supplementary information
Supplementary data are available at Bioinformatics online.
SUBMITTER: Wang Z
PROVIDER: S-EPMC8479658 | biostudies-literature |
REPOSITORIES: biostudies-literature