STARSEQ
1.2.1Secondary Trait Association analysis for Rare variants via SEQuence data
Overview
STARSEQ is an R-package for detecting associations with rare variants using selected samples in sequence-based association studies. It corrects for the bias in the secondary trait distribution induced by selective sampling on the primary trait. The corrected secondary trait can be analyzed by standard rare variant tests. In the STARSEQ package, several popular rare variant tests were implemented, which include 1.) combined multivariate and collapsing 2.) weighted sum statistics, 3.) kernel based adaptive cluster, 4.) variable threshold test 5.) sequence kernel association test.
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- 3.0 median / 9 max
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People & History
2 releases. Pick two to compare their code metrics. R releases are shown for context.
- RR 3.2.0 released · 2015-04-16
- archivedRemoved from CRAN2014-10-31never updated despite multiple reminders
- RR 3.1.0 released · 2014-04-10
- RR 3.0.0 released · 2013-04-03
- 1.2.12012-05-15 · diff ↗
- 1.022012-05-15
- RR 2.15.0 released · 2012-03-30
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- 2
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- GPL-3 OSI
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