Your search for returned 27 results

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Resource

Benchmarking small-variant genotyping in polyploids

  • First Published December 29, 2021
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
Research

The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes

  • First Published March 11, 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
Resource

Dindel: Accurate indel calls from short-read data

  • First Published October 27, 2010
Resource

Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads

  • First Published October 27, 2010
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