Reference panel-guided super-resolution inference of Hi-C data

被引:2
|
作者
Zhang, Yanlin [1 ]
Blanchette, Mathieu [1 ]
机构
[1] McGill Univ, Sch Comp Sci, Montreal, PQ H3A 0E9, Canada
关键词
GENOME; PRINCIPLES;
D O I
10.1093/bioinformatics/btad266
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
MotivationAccurately assessing contacts between DNA fragments inside the nucleus with Hi-C experiment is crucial for understanding the role of 3D genome organization in gene regulation. This challenging task is due in part to the high sequencing depth of Hi-C libraries required to support high-resolution analyses. Most existing Hi-C data are collected with limited sequencing coverage, leading to poor chromatin interaction frequency estimation. Current computational approaches to enhance Hi-C signals focus on the analysis of individual Hi-C datasets of interest, without taking advantage of the facts that (i) several hundred Hi-C contact maps are publicly available and (ii) the vast majority of local spatial organizations are conserved across multiple cell types.ResultsHere, we present RefHiC-SR, an attention-based deep learning framework that uses a reference panel of Hi-C datasets to facilitate the enhancement of Hi-C data resolution of a given study sample. We compare RefHiC-SR against tools that do not use reference samples and find that RefHiC-SR outperforms other programs across different cell types, and sequencing depths. It also enables high-accuracy mapping of structures such as loops and topologically associating domains.
引用
收藏
页码:i386 / i393
页数:8
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