How best to identify chromosomal interactions: a comparison of approaches

被引:109
作者
Davies, James O. J. [1 ]
Oudelaar, A. Marieke [1 ]
Higgs, Douglas R. [1 ]
Hughes, Jim R. [1 ]
机构
[1] Univ Oxford, Weatherall Inst Mol Med, Med Res Council MRC Mol Hematol Unit, Oxford, England
基金
英国惠康基金;
关键词
HI-C DATA; LONG-RANGE INTERACTIONS; ACTIVE CHROMATIN HUB; HIGH-RESOLUTION; DNA INTERACTIONS; GENOMIC INTERACTIONS; GENE PROMOTERS; GLOBIN LOCUS; HUMAN-CELLS; MICRO-C;
D O I
10.1038/nmeth.4146
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Chromosome conformation capture (3C) methods are central. to understanding the link between nuclear structure and function, and the physical interactions between distal regulatory elements and promoters. However, no one method is appropriate to address all biological questions, as each variant differs markedly in resolution, reproducibility, throughput and biases. A thorough appreciation of the strengths and weaknesses of each technique is critical when choosing the correct method for a specific application or for gauging how best to interpret different sources of data. In addition, the analysis method must be carefully considered, as this choice can profoundly affect the output. In this Review, we describe and compare the different available 3C-based approaches, with a focus on the analysis of mammalian genomes.
引用
收藏
页码:125 / 134
页数:10
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