SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.

TitleSimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.
Publication TypeJournal Article
Year of Publication2012
AuthorsLi, B, Wang, G, Leal, SM
JournalBioinformatics
Volume28
Issue20
Pagination2703-4
Date Published2012 Oct 15
ISSN1367-4811
KeywordsGenetic Association Studies, Genetic Variation, Humans, Phenotype, Quantitative Trait, Heritable, Software
Abstract

MOTIVATION: Currently, there is great interest in detecting complex trait rare variant associations using next-generation sequence data. On a monthly basis, new rare variant association methods are published. It is difficult to evaluate these methods because there is no standard to generate data and often comparisons are biased. In order to fairly compare rare variant association methods, it is necessary to generate data using realistic population demographic and phenotypic models.

RESULT: SimRare is an interactive program that integrates generation of rare variant genotype/phenotype data and evaluation of association methods using a unified platform. Variant data are generated for gene regions using forward-time simulation that incorporates realistic population demographic and evolutionary scenarios. Phenotype data can be obtained for both case-control and quantitative traits. SimRare has a user-friendly interface that allows for easy entry of genetic and phenotypic parameters. Novel rare variant association methods implemented in R can also be imported into SimRare, to evaluate their performance and compare results, e.g. power and Type I error, with other currently available methods both numerically and graphically.

DOI10.1093/bioinformatics/bts499
Alternate JournalBioinformatics
PubMed ID22914216
PubMed Central IDPMC3467746
Grant ListU54 HG006493 / HG / NHGRI NIH HHS / United States
HG006493 / HG / NHGRI NIH HHS / United States
HL102926 / HL / NHLBI NIH HHS / United States
UM1 HG006493 / HG / NHGRI NIH HHS / United States
MD005964 / MD / NIMHD NIH HHS / United States