Small sample properties of rare variant analysis methods

Michael D. Swartz, Taebeom Kim, Jiangong Niu, Robert K. Yu, Sanjay Shete, Iuliana Ionita-Laza

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

We are now well into the sequencing era of genetic analysis, and methods to investigate rare variants associated with disease remain in high demand. Currently, the more common rare variant analysis methods are burden tests and variance component tests. This report introduces a burden test known as the modified replication based sum statistic and evaluates its performance, and the performance of other common burden and variance component tests under the setting of a small sample size (103 total cases and controls) using the Genetic Analysis Workshop 18 simulated data with complete knowledge of the simulation model. Specifically we look at the variable threshold sum statistic, replication-based sum statistics, the C-alpha, and sequence kernel association test. Using minor allele frequency thresholds of less than 0.05, we find that the modified replication based sum statistic is competitive with all methods and that using 103 individuals leads to all methods being vastly underpowered. Much larger sample sizes are needed to confidently find truly associated genes.

Original languageEnglish (US)
Article numberS13
JournalBMC Proceedings
Volume8
DOIs
StatePublished - Jun 17 2014

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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