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RVtests (version 1.0)

VTWOD: VT and WOD for RV Tests

Description

Include methods: T1, T5, WE, VT, and WOD, which were described in the references below.

Usage

VTWOD(x, y, polyphen.weight, flipPhenotype = 0, npermutation = 1000, npermutation.max, min.nonsignificant.counts)

Arguments

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, if missing, equal to npermutation.
min.nonsignificant.counts
Minimum nonsignificant counts, if missing, equal to 10.

Value

  • scoreScores of T1, T5, WE, VT, and WOD
  • nonsignificant.countsCounts of permuted data that have a higher score than unpermuted data.
  • pvalue.empiricalEmpirical pvalue via permutation
  • pvalue.nominalTheoretical pvalue, not available now.
  • total.permutationTotal permutation

References

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.

See Also

RR, PCR, PLS