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
Simultaneous profiling of host expression and microbial abundance by spatial metatranscriptome sequencing
- First Published March 27, 2023
Research
Genomic analyses of wild argali, domestic sheep, and their hybrids provide insights into chromosome evolution, phenotypic variation, and germplasm innovation
- First Published August 10, 2022
Resource
Comprehensive variation discovery and recovery of missing sequence in the pig genome using multiple de novo assemblies
- First Published September 19, 2016
Method
TIGRA: A targeted iterative graph routing assembler for breakpoint assembly
- First Published December 4, 2013
Research
Locus co-occupancy, nucleosome positioning, and H3K4me1 regulate the functionality of FOXA2-, HNF4A-, and PDX1-bound loci in islets and liver
- First Published June 15, 2010
Research
The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance
- First Published April 29, 2010
Resource
A SNP discovery method to assess variant allele probability from next-generation resequencing data
- First Published December 17, 2009