Revealing Hi-C subcompartments by imputing inter-chromosomal chromatin interactions

被引:78
|
作者
Xiong, Kyle [1 ,2 ]
Ma, Jian [2 ]
机构
[1] Joint Carnegie Mellon Univ Univ Pittsburgh PhD Pr, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Sch Comp Sci, Computat Biol Dept, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
GENOME STRUCTURE POPULATIONS; DOMAINS; ORGANIZATION; ARCHITECTURE; PRINCIPLES; HETEROCHROMATIN; ENHANCERS; CONTACTS; PROVIDES; SYSTEM;
D O I
10.1038/s41467-019-12954-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Higher-order genome organization and its variation in different cellular conditions remain poorly understood. Recent high-coverage genome-wide chromatin interaction mapping using Hi-C has revealed spatial segregation of chromosomes in the human genome into distinct subcompartments. However, subcompartment annotation, which requires Hi-C data with high sequencing coverage, is currently only available in the GM12878 cell line, making it impractical to compare subcompartment patterns across cell types. Here we develop a computational approach, SNIPER (Subcompartment iNference using Imputed Probabilistic ExpRessions), based on denoising autoencoder and multilayer perceptron classifier to infer subcompartments using typical Hi-C datasets with moderate coverage. SNIPER accurately reveals subcompartments using moderate coverage Hi-C datasets and outperforms an existing method that uses epigenomic features in GM12878. We apply SNIPER to eight additional cell lines and find that chromosomal regions with conserved and cell-type specific subcompartment annotations have different patterns of functional genomic features. SNIPER enables the identification of subcompartments without high-coverage Hi-C data and provides insights into the function and mechanisms of spatial genome organization variation across cell types.
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页数:12
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