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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

cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis" > Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis

  • First Published October 11, 2017
Method

Co-expression networks reveal the tissue-specific regulation of transcription and splicing

  • First Published October 11, 2017
Research

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

  • First Published March 11, 2013
Resource

Annotation of functional variation in personal genomes using RegulomeDB

  • First Published September 5, 2012
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