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Paper Details

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.
Genomics
22
2019
Alzheimer's Disease, Alzheimer's disease, Atlas, Atlas SNVs, Atlas indels, GATK, SNV, SNVs, autosomal bi-allelic SNVs, indels, insertion-deletion variants, single nucleotide variants, whole genome
Author NameAffiliation
Honghuang LinBoston University School of Medicine
Badri N VardarajanColumbia University Medical Center
William S BushCase Western Reserve University
Najaf AminErasmus Medical Center
Seung Hoan ChoiBoston University School of Public Health
Seung Hoan ChoiBoston University School of Public Health
Namrata GuptaBroad Institute
Daniel C KoboldtInstitute for Genomic Medicine, Nationwide Children's Hospital
Li-San WangPerelman School of Medicine, University of Pennsylvania
Laura Adrienne CupplesBoston University School of Public Health
Cornelia M van DuijnErasmus Medical Center
Cornelia M van DuijnErasmus Medical Center
Gerard D SchellenbergPerelman School of Medicine, University of Pennsylvania
Eric BoerwinkleBaylor College of Medicine, University of Texas Health Science Center
Eric BoerwinkleBaylor College of Medicine, University of Texas Health Science Center
Joshua C BisCardiovascular Health Research Unit, University of Washington
Josée DupuisBoston University School of Public Health
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Datasets

Release 1.2