Power analysis and sample size estimation for sequence-based association studies.

TitlePower analysis and sample size estimation for sequence-based association studies.
Publication TypeJournal Article
Year of Publication2014
AuthorsWang, GT, Li, B, Santos-Cortez, RPLyn, Peng, B, Leal, SM
JournalBioinformatics
Volume30
Issue16
Pagination2377-8
Date Published2014 Aug 15
ISSN1367-4811
KeywordsAlleles, Data Interpretation, Statistical, Disease, Genetic Association Studies, Genetic Variation, Humans, Phenotype, Sample Size, Sequence Analysis, DNA, Software
Abstract

MOTIVATION: Statistical methods have been developed to test for complex trait rare variant (RV) associations, in which variants are aggregated across a region, which is typically a gene. Power analysis and sample size estimation for sequence-based RV association studies are challenging because of the necessity to realistically model the underlying allelic architecture of complex diseases within a suitable analytical framework to assess the performance of a variety of RV association methods in an unbiased manner.

SUMMARY: We developed SEQPower, a software package to perform statistical power analysis for sequence-based association data under a variety of genetic variant and disease phenotype models. It aids epidemiologists in determining the best study design, sample size and statistical tests for sequence-based association studies. It also provides biostatisticians with a platform to fairly compare RV association methods and to validate and assess novel association tests.

AVAILABILITY AND IMPLEMENTATION: The SEQPower program, source code, multi-platform executables, documentation, list of association tests, examples and tutorials are available at http://bioinformatics.org/spower.

DOI10.1093/bioinformatics/btu296
Alternate JournalBioinformatics
PubMed ID24778108
PubMed Central IDPMC4133582
Grant ListU54 HG006493 / HG / NHGRI NIH HHS / United States
UC2 HL102926 / HL / NHLBI NIH HHS / United States
P30 CA016672 / CA / NCI NIH HHS / United States
RC2 HL102926 / HL / NHLBI NIH HHS / United States
RC4 MD005964 / MD / NIMHD NIH HHS / United States
R01 HG005859 / HG / NHGRI NIH HHS / United States
CA016672 / CA / NCI 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
HG005859 / HG / NHGRI NIH HHS / United States
MD005964 / MD / NIMHD NIH HHS / United States