simulRefseqCompatibleWithVcf | R Documentation |
Simulate a reference genome sequence compatible with alleles from genotype data in the VCF format. Useful with the GATK software.
simulRefseqCompatibleWithVcf(
vcf.file = NULL,
vcf.rng.all = NULL,
chr.lengths = 10^5,
fa.file = NULL,
seed = NULL,
verbose = 1
)
vcf.file |
path to the file in the VCF format (will be used only if |
vcf.rng.all |
data frame output from |
chr.lengths |
vector of chromosome lengths (if a single number, will be repeated, i.e. all chromosomes will have the ame length) |
fa.file |
path to the output file in the fasta format (will be compressed via |
seed |
seed for the pseudo-random number generator (will be set only if non-NULL) |
verbose |
verbosity level (0/1) |
invisible DNAStringSet
Timothee Flutre
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