Title | Power analysis and sample size estimation for sequence-based association studies. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | Wang, GT, Li, B, Santos-Cortez, RPLyn, Peng, B, Leal, SM |
Journal | Bioinformatics |
Volume | 30 |
Issue | 16 |
Pagination | 2377-8 |
Date Published | 2014 Aug 15 |
ISSN | 1367-4811 |
Keywords | Alleles, 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. |
DOI | 10.1093/bioinformatics/btu296 |
Alternate Journal | Bioinformatics |
PubMed ID | 24778108 |
PubMed Central ID | PMC4133582 |
Grant List | U54 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 |