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Deep generative modeling and clustering of single cell Hi -C data
被引:9
|作者:
Liu, Qiao
[1
]
Zengt, Wanwen
[1
]
Zhang, Wei
[2
]
Wang, Sicheng
[3
]
Chen, Hongyang
[4
]
Jiang, Rui
[5
]
Zhou, Mu
[6
]
Zhang, Shaoting
[7
]
机构:
[1] Stanford Univ, Dept Stat, Stanford, CA USA
[2] Shandong Univ, Dept Biomed Engn, Jinan, Peoples R China
[3] UCSD, Dept Comp Sci & Engn, La Jolla, CA USA
[4] Zhejiang Lab, Hangzhou, Peoples R China
[5] Tsinghua Univ, Dept Automat, Beijing, Peoples R China
[6] Rutgers State Univ, Dept Comp Sci, New Brunswick, NJ USA
[7] Shanghai Artificial Intelligence Lab, Shanghai, Peoples R China
基金:
中国国家自然科学基金;
关键词:
single cell;
3D genome;
deep learning;
unsupervised learning;
CHROMATIN ACCESSIBILITY;
REVEALS PRINCIPLES;
GENOME;
TECHNOLOGIES;
D O I:
10.1093/bib/bbac494
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Deciphering 3D genome conformation is important for understanding gene regulation and cellular function at a spatial level. The recent advances of single cell Hi -C technologies have enabled the profiling of the 3D architecture of DNA within individual cell, which allows us to study the cell -to -cell variability of 3D chromatin organization. Computational approaches are in urgent need to comprehensively analyze the sparse and heterogeneous single cell Hi -C data. Here, we proposed scDEC-Hi-C, a new framework for single cell Hi -C analysis with deep generative neural networks. scDEC-Hi-C outperforms existing methods in terms of single cell Hi -C data clustering and imputation. Moreover, the generative power of scDEC-Hi-C could help unveil the differences of chromatin architecture across cell types. We expect that scDEC-Hi-C could shed light on deepening our understanding of the complex mechanism underlying the formation of chromatin contacts.
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页数:10
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