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SnapHiC: a computational pipeline to identify chromatin loops from single-cell Hi-C data

Single-cell Hi-C (scHi-C) analysis has been increasingly used to map chromatin architecture in diverse tissue contexts, but computational tools to define chromatin loops at high resolution from scHi-C data are still lacking. Here, we describe Single-Nucleus Analysis Pipeline for Hi-C (SnapHiC), a me...

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Detalles Bibliográficos
Autores principales: Yu, Miao, Abnousi, Armen, Zhang, Yanxiao, Li, Guoqiang, Lee, Lindsay, Chen, Ziyin, Fang, Rongxin, Lagler, Taylor M., Yang, Yuchen, Wen, Jia, Sun, Quan, Li, Yun, Ren, Bing, Hu, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440170/
https://www.ncbi.nlm.nih.gov/pubmed/34446921
http://dx.doi.org/10.1038/s41592-021-01231-2
Descripción
Sumario:Single-cell Hi-C (scHi-C) analysis has been increasingly used to map chromatin architecture in diverse tissue contexts, but computational tools to define chromatin loops at high resolution from scHi-C data are still lacking. Here, we describe Single-Nucleus Analysis Pipeline for Hi-C (SnapHiC), a method that can identify chromatin loops at high resolution and accuracy from scHi-C data. Using scHi-C data from 742 mouse embryonic stem cells, we benchmark SnapHiC against a number of computational tools developed for mapping chromatin loops and interactions from bulk Hi-C. We further demonstrate its use by analyzing single-nucleus methyl-3C-seq data from 2,869 human prefrontal cortical cells, which uncovers cell type-specific chromatin loops and predicts putative target genes for noncoding sequence variants associated with neuropsychiatric disorders. Our results indicate that SnapHiC could facilitate the analysis of cell type-specific chromatin architecture and gene regulatory programs in complex tissues.