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Deep generative modeling and clustering of single cell Hi-C data.

Qiao LiuWanwen ZengWei ZhangSicheng WangHongyang ChenRui JiangMu ZhouShaoting Zhang
Published in: Briefings in bioinformatics (2022)
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.
Keyphrases
  • single cell
  • rna seq
  • high throughput
  • gene expression
  • dna damage
  • neural network
  • electronic health record
  • big data
  • cell therapy
  • mesenchymal stem cells
  • data analysis