ESP cohort

Aliases

Exome Sequencing Project, NHLBI GO Exome Sequencing Project

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Mentioned in (8)

Papers in which this entity is mentioned.

• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• CRAVAT 4: Cancer-Related Analysis of Variants Toolkit. (2017)
• A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. (2016)
• VariantDB: a flexible annotation and filtering portal for next generation sequencing data. (2014)
• Signatures of mutational processes in human cancer. (2013)
• Genic intolerance to functional variation and the interpretation of personal genomes. (2013)

Merged raw entities (3)

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