Your search for returned 32 results

Order by:
Show per page

Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T

  • First Published March 17, 2025

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

A harmonized public resource of deeply sequenced diverse human genomes

  • First Published May 15, 2024

Discordant calls across genotype discovery approaches elucidate variants with systematic errors

  • First Published May 30, 2023

Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotides

  • First Published June 1, 2018

Spark: A navigational paradigm for genomic data exploration

  • First Published September 7, 2012

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

The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance

  • First Published April 29, 2010

The completion of the Mammalian Gene Collection (MGC)

  • First Published September 18, 2009

ABySS: A parallel assembler for short read sequence data

  • First Published February 27, 2009
Show per page