Read clouds uncover variation in complex regions of the human genome
- First Published August 18, 2015
The use of exome capture RNA-seq for highly degraded RNA with application to clinical cancer sequencing
- First Published August 7, 2015
Discovery of recurrent structural variants in nasopharyngeal carcinoma
- First Published November 8, 2013
HIV infection reveals widespread expansion of novel centromeric human endogenous retroviruses
- First Published May 8, 2013
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
- First Published March 11, 2013
Ubiquitous heterogeneity and asymmetry of the chromatin environment at regulatory elements
- First Published September 5, 2012
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia
- First Published September 5, 2012
Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes
- First Published January 12, 2010