Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts

Understanding the impact of rare variants is essential to understanding human health. We analyze rare (MAF 

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Bibliographic Details
Published in:Nature communications 2020-01, Vol.11 (1), p.542-542, Article 542
Main Authors: Cirulli, Elizabeth T., White, Simon, Read, Robert W., Elhanan, Gai, Metcalf, William J., Tanudjaja, Francisco, Fath, Donna M., Sandoval, Efren, Isaksson, Magnus, Schlauch, Karen A., Grzymski, Joseph J., Lu, James T., Washington, Nicole L.
Format: Article
Language:English
Subjects:
45
45/23
45/43
49
631/208/205
631/208/457/649/2219
631/208/514/2254
692/308/2056
Adolescent
Adult
Aged
Aged, 80 and over
Biobanks
Browsing
Cohort Studies
Databases, Genetic
Europe
Exome - genetics
Female
Genetic analysis
Genetic diversity
Genetic variance
Genetic Variation
Genetics, Population - statistics & numerical data
Genome, Human
Genome-Wide Association Study
Genomes
Genotyping
High-Throughput Nucleotide Sequencing
Humanities and Social Sciences
Humans
Male
Meta-Analysis as Topic
Middle Aged
multidisciplinary
Phenotype
Phenotypes
Science
Science (multidisciplinary)
Software
Statistical analysis
Test procedures
Whole Exome Sequencing
Young Adult
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Description
Summary:Understanding the impact of rare variants is essential to understanding human health. We analyze rare (MAF 
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-020-14288-y