readVCF: Read a vcf file, with options to filter out low or high...

In sim1000G: Genotype Simulations for Rare or Common Variants Using Haplotypes from 1000 Genomes

Description

Read a vcf file, with options to filter out low or high frequency markers.

Usage

readVCF(filename = "data.vcf", thin = NA, maxNumberOfVariants = 400,
  min_maf = 0.02, max_maf = NA, region_start = NA, region_end = NA)

Arguments

filename	Input VCF file
thin	How much to thin markers
maxNumberOfVariants	Maximum number of variants to keep from region
min_maf	Minimum allele frequency of markers to keep. If NA skip min_maf filtering.
max_maf	Maximum allele frequency of markers to keep. If NA skip max_maf filtering.
region_start	Extract a region from a vcf files with this starting basepair position
region_end	Extract a region from a vcf files with this ending basepair position

Value

VCF object to be used by startSimulation function.

Examples

examples_dir = system.file("examples", package = "sim1000G")
vcf_file = file.path(examples_dir,
  "region-chr4-93-TMEM156.vcf.gz")

vcf = readVCF( vcf_file, maxNumberOfVariants = 500 ,
               min_maf = 0.02 ,max_maf = NA)

str(as.list(vcf))

sim1000G documentation built on June 10, 2019, 1:01 a.m.