Research
Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T
- First Published March 17, 2025
Research
Rearrangements of viral and human genomes at human papillomavirus integration events and their allele-specific impacts on cancer genome regulation
- First Published December 5, 2024
Resource
Binding profiles for 961 Drosophila and C. elegans transcription factors reveal tissue-specific regulatory relationships
- First Published October 22, 2024
Resource
Comprehensive characterization of tissue-specific chromatin accessibility in L2 Caenorhabditis elegans nematodes
- First Published April 22, 2021
Method
Ancestry-agnostic estimation of DNA sample contamination from sequence reads
- First Published January 24, 2020
Resource
The C. elegans embryonic transcriptome with tissue, time, and alternative splicing resolution
- First Published May 23, 2019
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