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Regie P. Lyn Santos-Cortez

dblp:150/0090 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2014
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › statistical genetics
genetic association study
0.212014
Power analysis and sample size estimation for sequence-based association studies · Bioinform. 2014
Bioinformatics and computational biology › statistical genetics › rare variant analysis
rare variant association testing
0.212014
Power analysis and sample size estimation for sequence-based association studies · Bioinform. 2014
Bioinformatics and computational biology › biostatistics
sample size determination
0.212014
Power analysis and sample size estimation for sequence-based association studies · Bioinform. 2014

Methods — techniques the papers use, named apart from their topics

statistical power analysis · 0.2
YearPublicationVenuePosition
2014 Power analysis and sample size estimation for sequence-based association studies
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.
Gao T. Wang, Regie P. Lyn Santos-Cortez, Suzanne M. Leal
Bioinform.3