Method
Copolymerization of single-cell nucleic acids into balls of acrylamide gel
- First Published November 14, 2019
Method
SMASH, a fragmentation and sequencing method for genomic copy number analysis
- First Published April 14, 2016
Method
Read clouds uncover variation in complex regions of the human genome
- First Published August 18, 2015
Method
Optimizing sparse sequencing of single cells for highly multiplex copy number profiling
- First Published April 9, 2015
Method
Discovery of recurrent structural variants in nasopharyngeal carcinoma
- First Published November 8, 2013
Research
The maize methylome influences mRNA splice sites and reveals widespread paramutation-like switches guided by small RNA
- First Published June 5, 2013
Research
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
- First Published March 11, 2013
Resource
Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors
- First Published September 5, 2012
Method
Ubiquitous heterogeneity and asymmetry of the chromatin environment at regulatory elements
- First Published September 5, 2012