Research
Complex mosaic structural variations in human fetal brains
- First Published October 29, 2020
Resource
Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562
- First Published February 8, 2019
Method
Read clouds uncover variation in complex regions of the human genome
- First Published August 18, 2015
Method
Discovery of recurrent structural variants in nasopharyngeal carcinoma
- First Published November 8, 2013
Research
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals
- First Published October 3, 2013
Research
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
- First Published March 11, 2013
Method
Ubiquitous heterogeneity and asymmetry of the chromatin environment at regulatory elements
- First Published September 5, 2012
Resource
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia
- First Published September 5, 2012
Resource
CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing
- First Published February 7, 2011