Coverage recommendations for methylation analysis by whole-genome bisulfite sequencing

被引:0
|
作者
Ziller M.J. [1 ,2 ,3 ]
Hansen K.D. [4 ,5 ]
Meissner A. [1 ,2 ,3 ]
Aryee M.J. [1 ,6 ,7 ,8 ]
机构
[1] Broad Institute of MIT and Harvard, Cambridge, MA
[2] Harvard Stem Cell Institute, Cambridge, MA
[3] Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA
[4] McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins School of Medicine, Baltimore, MD
[5] Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD
[6] Molecular Pathology Unit, Massachusetts General Hospital, Charlestown, MA
[7] Center for Cancer Research, Massachusetts General Hospital, Charlestown, MA
[8] Department of Pathology, Harvard Medical School, Boston, MA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nmeth.3152
中图分类号
学科分类号
摘要
Whole-genome bisulfite sequencing (WGBS) allows genome-wide DNA methylation profiling, but the associated high sequencing costs continue to limit its widespread application. We used several high-coverage reference data sets to experimentally determine minimal sequencing requirements. We present data-derived recommendations for minimum sequencing depth for WGBS libraries, highlight what is gained with increasing coverage and discuss the trade-off between sequencing depth and number of assayed replicates. © 2015 Nature America, Inc.
引用
收藏
页码:230 / 232
页数:2
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