Document Type
Article
Publication Date
11-25-2019
Keywords
JGM
JAX Source
Genome Biol 2019 Nov 25; 20(1):251
Volume
20
Issue
1
First Page
251
Last Page
251
ISSN
1474-760X
PMID
31767038
DOI
https://doi.org/10.1186/s13059-019-1868-z
Grant
Jackson Laboratory Director's Innovation Fund, HG009409, DK107967, Human Frontier Science Program, Florine Roux Endowment
Abstract
The single-molecule multiplex chromatin interaction data are generated by emerging 3D genome mapping technologies such as GAM, SPRITE, and ChIA-Drop. These datasets provide insights into high-dimensional chromatin organization, yet introduce new computational challenges. Thus, we developed MIA-Sig, an algorithmic solution based on signal processing and information theory. We demonstrate its ability to de-noise the multiplex data, assess the statistical significance of chromatin complexes, and identify topological domains and frequent inter-domain contacts. On chromatin immunoprecipitation (ChIP)-enriched data, MIA-Sig can clearly distinguish the protein-associated interactions from the non-specific topological domains. Together, MIA-Sig represents a novel algorithmic framework for multiplex chromatin interaction analysis.
Recommended Citation
Kim M,
Zheng M,
Tian S,
Lee B,
Chuang J,
Ruan Y.
MIA-Sig: multiplex chromatin interaction analysis by signal processing and statistical algorithms. Genome Biol 2019 Nov 25; 20(1):251
Comments
This open access article is licensed under a Creative Commons Attribution 4.0 International License