Method
Secure phasing of private genomes in a trusted execution environment with TX-Phase
- First Published November 12, 2025
Method
Genotyping of selected germline adaptive immune system loci using short-read sequencing data
- First Published August 5, 2025
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
Method
Single-cell methylation sequencing data reveal succinct metastatic migration histories and tumor progression models
- First Published June 14, 2023
Method
An efficient genotyper and star-allele caller for pharmacogenomics
- First Published January 19, 2023
Method
Enzymatic methyl sequencing detects DNA methylation at single-base resolution from picograms of DNA
- First Published June 17, 2021
Method
PhISCS: a combinatorial approach for subperfect tumor phylogeny reconstruction via integrative use of single-cell and bulk sequencing data
- First Published October 18, 2019
Method
HIT'nDRIVE: patient-specific multidriver gene prioritization for precision oncology
- First Published July 18, 2017
Method
nFuse: Discovery of complex genomic rearrangements in cancer using high-throughput sequencing
- First Published June 28, 2012