Description Usage Arguments Value See Also Examples

Compute p-values and likelihoods of all possible models for a given number of disease SNP(s).

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`n.fp` |
number of disease SNPs for tests. |

`genoT` |
matrix of control genotypes. Each row indicates a variant, and each column indicates a haplotype of an individual. Two alleles of 0 and 1 are available. |

`genoC` |
matrix of case genotypes. Each row indicates a variant, and each column indicates a haplotype of an individual. Two alleles of 0 and 1 are available. |

matrix of likelihood ratio test results. First row indicates the index, and following n.fp rows indicate the model for each set of disease polymorphisms, and followed by p-values, -2 log(likelihood ratio) with corrections for variances, and the degree of freedom.

allele.freq.G

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IFP documentation built on May 29, 2017, 9:07 p.m.

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