geno.freq


  matrix of haplotypes. Each row indicates a variant, and each column ind
icates a haplotype of an individual. Two alleles of 0 and 1 are available.


genoG


 Computes genotype frequencies from the sequencing data with a vcf type of the 1000 Genomes Project. 


A suite for identifying causal models using relative concordances and identifying causal polymorphisms in case-control genetic association data, especially with large controls re-sequenced data.

geno.freq: Genotype Frequency Computation from the sequencing data with a vcf type of the 1000 Genomes Project

Description

Usage

Arguments

Value

Examples