Sizing up whole-genome sequencing studies of common diseases
Sign Up to like & getrecommendations! Published in 2018 at "Nature Genetics"
DOI: 10.1038/s41588-018-0113-0
Abstract: The triplet code underpins analyses of rare and de novo mutations in exome sequencing data, but analysis of the noncoding genome is much more challenging. A new analytical framework for common, complex diseases highlights the… read more here.
Keywords: studies common; whole genome; common diseases; sizing whole ... See more keywords