Publication

Identifying rare variants from exome scans: the GAW17 experience

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Last modified
  • 02/20/2025
Type of Material
Authors
    Saurabh Ghosh, Indian Statistical InstituteHeike Bickeboller, University of GöttingenJulia Bailey, University of CaliforniaJoan E. Bailey-Wilson, National Human Genome Research InstituteRita Cantor, University of CaliforniaRobert Culverhouse, Washington UniversityWarwick Daw, Washington UniversityAnita L. DeStefano, Boston UniversityCorinne D. Engelman, University of Wisconsin-MadisonAnthony Hinrichs, Washington UniversityJeanine Houwing-Duistermaat, Leiden UniversityInke R. Konig, Universität zu LübeckJack Kent, Jr., Texas Biomedical Research InstituteNan Laird, HarvardNathan Pankratz, University of MinnesotaAndrew Paterson, University of TorontoElizabeth Pugh, Johns Hopkins UniversityBrian Suarez, Washington UniversityYan Sun, Emory UniversityAlun Thomas, University of UtahNathan Tintle, Dordt CollegeXiaofeng Zhu, Case Western Reserve UniversityAndreas Ziegler, Universität zu LübeckJean W. MacCluer, Texas Biomedical Research InstituteLaura Almasy, Texas Biomedical Research Institute
Language
  • English
Date
  • 2011-11-29
Publisher
  • BioMed Central
Publication Version
Copyright Statement
  • © 2011 Ghosh et al; licensee BioMed Central Ltd.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1753-6561
Volume
  • 5
Issue
  • Suppl 9
Start Page
  • 1
End Page
  • 4
Grant/Funding Information
  • This grant also provided scholarship funds to help defray travel costs for 40 graduate students and postdoctoral trainees attending GAW17
  • Continuous funding for the Genetic Analysis Workshops has been provided since 1982 by the National Institute of General Medical Sciences (NIGMS), through National Institutes of Health grant R01 GM31575 awarded to Jean MacCluer and Laura Almasy.
Abstract
  • Genetic Analysis Workshop 17 (GAW17) provided a platform for evaluating existing statistical genetic methods and for developing novel methods to analyze rare variants that modulate complex traits. In this article, we present an overview of the 1000 Genomes Project exome data and simulated phenotype data that were distributed to GAW17 participants for analyses, the different issues addressed by the participants, and the process of preparation of manuscripts resulting from the discussions during the workshop.
Author Notes
Research Categories
  • Health Sciences, Epidemiology
  • Biology, Genetics
  • Biology, Biostatistics

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