Description Usage Arguments Value Note Author(s) References See Also
Include methods: T1, T5, WE, VT, and WOD.
1 2 | VTWOD(x, y, polyphen.weight, flipPhenotype = 0,
npermutation = 1000, npermutation.max, min.nonsignificant.counts)
|
x |
Genotype matrix |
y |
Phenotype vector |
polyphen.weight |
Polyphen weight |
flipPhenotype |
Logical, if TRUE, flip phenotype to opposite by multipling -1 |
npermutation |
Number of permutation, if less than 1, the permutation will not be run. |
npermutation.max |
Maximum permutation |
min.nonsignificant.counts |
Minimum nonsignificant counts |
score |
Scores of T1, T5, WE, VT, and WOD |
nonsignificant.counts |
Counts of permuted data that have a higher score than unpermuted data. |
pvalue.empirical |
Empirical pvalue via permutation |
pvalue.nominal |
Theoretical pvalue, not available now. |
total.permutation |
Total permutation |
This R implementation by Adam Kiezun, based on reference implementation in C by Alkes Price. Added WOD tests to the program in 2011 by Celia Greenwood
C. Xu, Celia Greenwood
Xu C, Ladouceur M, Dastani Z, Richards JB, Ciampi A, Greenwood CMT. (2012) Multiple Regression Methods Show Great Potential for Rare Variant Association Tests. PLoS ONE 7(8): e41694. doi:10.1371/journal.pone.0041694
Ladouceur M, Dastani Z, Aulchenko YS, Greenwood CM, Richards JB (2012) The empirical power of rare variant association methods: Results from sanger sequencing in 1,998 individuals. PloS Genetics 8: e1002496.
Price AL, Kryukov GV, de Bakker PI, Purcell SM, Staples J, et al. (2010) Pooled association tests for rare variants in exon-resequencing studies. Am J Hum Genet 86: 832 - 838.
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