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
An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data
- First Published April 16, 2015
Research
The influence of genomic context on mutation patterns in the human genome inferred from rare variants
- First Published August 29, 2013
Resource
Annotation of functional variation in personal genomes using RegulomeDB
- First Published September 5, 2012
Method
Linking disease associations with regulatory information in the human genome
- First Published September 5, 2012
Resource
Open chromatin defined by DNaseI and FAIRE identifies regulatory elements that shape cell-type identity
- First Published July 12, 2011
Resource
Low-coverage sequencing: Implications for design of complex trait association studies
- First Published April 1, 2011