HSA: integrating multi-track Hi-C data for genome-scale reconstruction of 3D chromatin structure

被引:49
|
作者
Zou, Chenchen [1 ]
Zhang, Yuping [2 ,3 ,6 ,7 ,8 ]
Ouyang, Zhengqing [1 ,3 ,4 ,5 ]
机构
[1] Jackson Lab Genom Med, Farmington, CT 06032 USA
[2] Univ Connecticut, Dept Stat, Storrs, CT 06269 USA
[3] Univ Connecticut, Inst Syst Genom, Farmington, CT 06030 USA
[4] Univ Connecticut, Dept Biomed Engn, Storrs, CT 06269 USA
[5] Univ Connecticut, Dept Genet & Genome Sci, Farmington, CT 06030 USA
[6] Univ Connecticut, Inst Collaborat Hlth Intervent & Policy, Storrs, CT 06269 USA
[7] Univ Connecticut, Ctr Quantitat Med, Farmington, CT 06030 USA
[8] Univ Connecticut, Connecticut Inst Brain & Cognit Sci, Storrs, CT 06269 USA
来源
GENOME BIOLOGY | 2016年 / 17卷
关键词
Hi-C; 3D chromatin structure; Multi-track modeling; Markov chain; Simulated annealing; CHROMOSOMAL INTERACTIONS; ORGANIZATION; FREQUENCY; BIASES;
D O I
10.1186/s13059-016-0896-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genome-wide 3C technologies (Hi-C) are being increasingly employed to study three-dimensional (3D) genome conformations. Existing computational approaches are unable to integrate accumulating data to facilitate studying 3D chromatin structure and function. We present HSA (http://ouyanglab.jax.org/hsa/), a flexible tool that jointly analyzes multiple contact maps to infer 3D chromatin structure at the genome scale. HSA globally searches the latent structure underlying different cleavage footprints. Its robustness and accuracy outperform or rival existing tools on extensive simulations and orthogonal experiment validations. Applying HSA to recent in situ Hi-C data, we found the 3D chromatin structures are highly conserved across various human cell types.
引用
收藏
页数:14
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