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Read clouds uncover variation in complex regions of the human genome

  • First Published August 18, 2015

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

  • First Published January 30, 2015

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

  • First Published October 1, 2014

Genome evolution during progression to breast cancer

  • First Published April 8, 2013

Ubiquitous heterogeneity and asymmetry of the chromatin environment at regulatory elements

  • First Published September 5, 2012

Linking disease associations with regulatory information in the human genome

  • First Published September 5, 2012

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

  • First Published September 5, 2012

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

  • First Published July 10, 2009

Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome

  • First Published June 13, 2007

Græmlin: General and robust alignment of multiple large interaction networks

  • First Published August 9, 2006
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