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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Veröffentlicht in:	Nature communications 2020-01, Vol.11 (1), p.542-10, Article 542
Hauptverfasser:	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:	Artikel
Sprache:	eng
Schlagworte:	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 Exome Sequencing 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 Middle Aged multidisciplinary Phenotype Phenotypes Science Science (multidisciplinary) Software Statistical analysis Test procedures Young Adult
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Beschreibung
Zusammenfassung:	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