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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
Resource

The completion of the Mammalian Gene Collection (MGC)

  • First Published September 18, 2009
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