Reconstructing 3D chromosome structures from single-cell Hi-C data with SO(3)-equivariant graph neural networks.
Journal:
NAR genomics and bioinformatics
PMID:
40124711
Abstract
The spatial conformation of chromosomes and genomes of single cells is relevant to cellular function and useful for elucidating the mechanism underlying gene expression and genome methylation. The chromosomal contacts (i.e. chromosomal regions in spatial proximity) entailing the three-dimensional (3D) structure of the genome of a single cell can be obtained by single-cell chromosome conformation capture techniques, such as single-cell Hi-C (ScHi-C). However, due to the sparsity of chromosomal contacts in ScHi-C data, it is still challenging for traditional 3D conformation optimization methods to reconstruct the 3D chromosome structures from ScHi-C data. Here, we present a machine learning-based method based on a novel SO(3)-equivariant graph neural network (HiCEGNN) to reconstruct 3D structures of chromosomes of single cells from ScHi-C data. HiCEGNN consistently outperforms both the traditional optimization methods and the only other deep learning method across diverse cells, different structural resolutions, and different noise levels of the data. Moreover, HiCEGNN is robust against the noise in the ScHi-C data.