Genotyping Array Design and Data Quality Control in the Million Veteran Program.

doi:10.1016/j.ajhg.2020.03.004

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Genotyping Array Design and Data Quality Control in the Million Veteran Program.

American journal of human genetics - 2 Apr 2020

Hunter-Zinck Haley, Shi Yunling, Li Man, Gorman Bryan R, Ji Sun-Gou, Sun Ning, Webster Teresa, Liem Andrew, Hsieh Paul, Devineni Poornima, Karnam Purushotham, Gong Xin, Radhakrishnan Lakshmi, Schmidt Jeanette, Assimes Themistocles L, Huang Jie, Pan Cuiping, Humphries Donald, Brophy Mary, Moser Jennifer, Muralidhar Sumitra, Huang Grant D, Przygodzki Ronald, Concato John, Gaziano John M, Gelernter Joel, O'Donnell Christopher J, Hauser Elizabeth R, Zhao Hongyu, O'Leary Timothy J, Tsao Philip S, Pyarajan Saiju

Abstract excerpt

The Million Veteran Program (MVP), initiated by the Department of Veterans Affairs (VA), aims to collect biosamples with consent from at least one million veterans. Presently, blood samples have been collected from over 800,000 enrolled participants. The size and diversity of the MVP cohort, as well as the availability of extensive VA electronic health records, make it a promising resource for precision medicine....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ethnicity

Share to Genetic Markers

Share to Genome-Wide Association Study

Share to Precision Medicine

Share to Quality Control

Share to Veterans

Share to Whole Genome Sequencing

Source

Open in PubMed Open full text

Identifiers

PMID: 32243820
DOI: 10.1016/j.ajhg.2020.03.004
PMCID: PMC7118558

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotyping Array Design and Data Quality Control in the Million Veteran Program.PMID 32243820Read ↗

Million Veteran Program: A mega-biobank to study genetic influences on health and disease.Semantic proximity Read ↗

Genotyping Informatics and Quality Control for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort.Semantic proximity Read ↗

Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran ProgramSemantic proximity Read ↗

Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.Semantic proximity Read ↗

MaveRegistry: a collaboration platform for multiplexed assays of variant effectSemantic proximity Read ↗

Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array.Semantic proximity Read ↗

Development of a clinical polygenic risk score assay and reporting workflow.Semantic proximity Read ↗

Pharmacogenetic allele variant frequencies: An analysis of the VA's Million Veteran Program (MVP) as a representation of the diversity in US population.Semantic proximity Read ↗

Pharmacogenetic allele variant frequencies: An analysis of the VA’s Million Veteran Program (MVP) as a representation of the diversity in US populationSemantic proximity Read ↗

Advancing Precision Medicine in the Korean Population: The Korea Biobank Array v2.0 as a Comprehensive Genomic ResourceSemantic proximity Read ↗

VN1K is a pangenome-informed multi-omics and phenomics resource for the Vietnamese population.Semantic proximity Read ↗

Variant association tools for quality control and analysis of large-scale sequence and genotyping array data.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.