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Paper Details

Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges.
Hum Mutat
10
2017
blood, genetic disorder, genome, genomes, whole
Author NameAffiliation
Biao LiThe Buck Institute for Research on Aging
Timothy BergquistUniversity of Washington School of Medicine
Hannah CarterInstitute for Genomic Medicine and Moores Cancer Center, University of California San Diego
Hannah CarterInstitute for Genomic Medicine and Moores Cancer Center, University of California San Diego
Melissa S ClineUniversity of California
Mark DiekhansUniversity of California
Mark DiekhansUniversity of California
Marco CarraroUniversity of Padova
Manuel GiolloUniversity of Padova
Manuel GiolloUniversity of Padova
Carlo FerrariUniversity of Padova
Silvio C E TosattoUniversity of Padova
Silvio C E TosattoCNR Neuroscience Institute
Silvio C E TosattoUniversity of Padova
Silvio C E TosattoCNR Neuroscience Institute
Jason Bobe
Roger A HoskinsUniversity of California berkeley
George M Church
George M Church
Steven E BrennerUniversity of California berkeley
Steven E BrennerUniversity of California berkeley
John MoultInstitute for Bioscience and Biotechnology Research, University of Maryland
John MoultUniversity of Maryland, College Park
Julian GoughUniversity of Bristol
Julian GoughUniversity of Bristol
Mario StankeInstitute of Mathematics and Computer Science, University of Greifswald
Rachel KarchinDepartment of Biomedical Engineering and Institute for Computational Medicine, Johns Hopkins University
Rachel KarchinThe Johns Hopkins Medical Institutions
Rachel KarchinDepartment of Biomedical Engineering and Institute for Computational Medicine, Johns Hopkins University
Rachel KarchinThe Johns Hopkins Medical Institutions
Sean D MooneyUniversity of Washington School of Medicine
Sean D MooneyUniversity of Washington School of Medicine
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