Single-cell Hi-C data analysis: safety in numbers

被引:21
|
作者
Galitsyna, Aleksandra A. [1 ]
Gelfand, Mikhail S. [2 ,3 ]
机构
[1] Skolkovo Inst Sci & Technol, Prof Gelfands Grp, Moscow, Russia
[2] Skolkovo Inst Sci & Technol, Ctr Life Sci, Moscow, Russia
[3] Skolkovo Inst Sci & Technol, Biomed Res, Moscow, Russia
基金
俄罗斯基础研究基金会;
关键词
single cell; chromatin; single-cell Hi-C; conformation capture; single-cell sequencing; 3-DIMENSIONAL GENOME STRUCTURES; CHROMOSOME CONFORMATION; CHROMATIN ARCHITECTURE; SYSTEMATIC BIASES; REVEALS; ORGANIZATION; DNA; DYNAMICS;
D O I
10.1093/bib/bbab316
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Over the past decade, genome-wide assays for chromatin interactions in single cells have enabled the study of individual nuclei at unprecedented resolution and throughput. Current chromosome conformation capture techniques survey contacts for up to tens of thousands of individual cells, improving our understanding of genome function in 3D. However, these methods recover a small fraction of all contacts in single cells, requiring specialised processing of sparse interactome data. In this review, we highlight recent advances in methods for the interpretation of single-cell genomic contacts. After discussing the strengths and limitations of these methods, we outline frontiers for future development in this rapidly moving field.
引用
收藏
页数:13
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