Article
Adaptive Fisher method detects dense and sparse signals in association analysis of SNV sets.
BMC medical genomics - 3 Apr 2020
Cai Xiaoyu, Chang Lo-Bin, Potter Jordan, Song Chi
Abstract excerpt
BACKGROUND: With the development of next generation sequencing (NGS) technology and genotype imputation methods, statistical methods have been proposed to test a set of genomic variants together to detect if any of them is associated with the phenotype or disease. In practice, within the set, there is an unknown proportion of variants truly causal or associated with the disease. There is a demand for statistical...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
