Method
Multiplexed long-read plasmid validation and analysis using OnRamp
- First Published May 8, 2023
Method
TRACE: transcription factor footprinting using chromatin accessibility data and DNA sequence
- First Published July 6, 2020
Method
Ancestry-agnostic estimation of DNA sample contamination from sequence reads
- First Published January 24, 2020
Method
Read clouds uncover variation in complex regions of the human genome
- First Published August 18, 2015
Method
An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data
- First Published April 16, 2015
Method
Discovery of recurrent structural variants in nasopharyngeal carcinoma
- First Published November 8, 2013
Research
The influence of genomic context on mutation patterns in the human genome inferred from rare variants
- First Published August 29, 2013
Research
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
- First Published March 11, 2013
