A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Lipids Working Group

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

STAARpipeline is a comprehensive framework for flexible and scalable rare-variant association analysis using whole-genome sequencing data and annotation information.

Original languageEnglish (US)
Pages (from-to)1599-1611
Number of pages13
JournalNature Methods
Volume19
Issue number12
DOIs
StatePublished - Dec 2022

Bibliographical note

Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature America, Inc. 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law..

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