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Resource

A harmonized public resource of deeply sequenced diverse human genomes

  • First Published May 15, 2024
Resource

Discordant calls across genotype discovery approaches elucidate variants with systematic errors

  • First Published May 30, 2023
Research

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

  • First Published June 1, 2018
Method

Read clouds uncover variation in complex regions of the human genome

  • First Published August 18, 2015
Method

Parente2: a fast and accurate method for detecting identity by descent

  • First Published October 1, 2014
Research

Genome evolution during progression to breast cancer

  • First Published April 8, 2013
Method

Ubiquitous heterogeneity and asymmetry of the chromatin environment at regulatory elements

  • First Published September 5, 2012
Resource

ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia

  • First Published September 5, 2012
Method

Linking disease associations with regulatory information in the human genome

  • First Published September 5, 2012
Letter

Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes

  • First Published January 12, 2010
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