GILoop: Robust chromatin loop calling across multiple sequencing depths on Hi-C data

被引:5
|
作者
Wang, Fuzhou [1 ]
Gao, Tingxiao [2 ]
Lin, Jiecong [3 ]
Zheng, Zetian [1 ]
Huang, Lei [1 ]
Toseef, Muhammad [1 ]
Li, Xiangtao [4 ]
Wong, Ka -Chun [1 ]
机构
[1] City Univ Hong Kong, Dept Comp Sci, Kowloon Tong, Hong Kong, Peoples R China
[2] Univ Toronto, Fac Med, Dept Med Biophys, Toronto, ON, Canada
[3] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Canc Res, Dept Pathol,Mol Pathol Unit, Boston, MA 02129 USA
[4] Jilin Univ, Sch Artificial Intelligence, Changchun 132000, Peoples R China
基金
中国国家自然科学基金;
关键词
GENOME ARCHITECTURE; REVEALS; PRINCIPLES; ORGANIZATION; BROWSER; MAP;
D O I
10.1016/j.isci.2022.105535
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
Graph and image are two common representations of Hi-C cis-contact maps. Existing computational tools have only adopted Hi-C data modeled as unitary data structures but neglected the potential advantages of synergizing the information of different views. Here we propose GILoop, a dual-branch neural network that learns from both representations to identify genome-wide CTCF-mediated loops. With GILoop, we explore the combined strength of integrating the two view representations of Hi-C data and corroborate the complementary relationship between the views. In particular, the model outperforms the state-of-the-art loop calling framework and is also more robust against low-quality Hi-C libraries. We also uncover distinct preferences for matrix density by graph-based and image-based models, revealing interesting insights into Hi-C data elucidation. Finally, along with multiple transfer-learning case studies, we demonstrate that GILoop can accurately model the organizational and functional patterns of CTCF-mediated looping across different cell lines.
引用
收藏
页数:25
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