Genome-wide significance
id:
genome-wide-significance-235-17207204
title:
Genome-wide significance
text:
In genome-wide association studies, genome-wide significance is a specific threshold for determining the statistical significance of a reported association between a given single-nucleotide polymorphism (SNP) and a given trait. The most commonly accepted threshold is p < 5 × 10−8, which is based on performing a Bonferroni correction for all the independent common SNPs across the human genome. If a p-value is found to be lower than this threshold in a genome-wide association study, the null hypot
brand slug:
wiki
category slug:
encyclopedia
description:
Statistical significance threshold for genetic associations
original url:
https://en.wikipedia.org/wiki/Genome-wide_significance
date created:
date modified:
2021-12-12T03:51:25Z
main entity:
{"identifier":"Q85763011","url":"https://www.wikidata.org/entity/Q85763011"}
image:
fields total:
13
integrity:
14