Displaying 2 results from an estimated 2 matches for "readgeneticmap".
2020 Oct 29
1
R: sim1000G
...vcf.gz" #nvariants = 442, ss=1000
vcf = readVCF( vcf_file, maxNumberOfVariants = 442 ,min_maf =
0.0005,max_maf = 0.01) #lowest MAF
dim( vcf$gt1 ) #rows represent number of variants, columns represent
number of individuals
## Download and use full chromosome genetic map
downloadGeneticMap(4)
readGeneticMap(4)
sample.size=3000
startSimulation(vcf, totalNumberOfIndividuals = sample.size)
data_sim = function(seed.num){
SIM$reset()
id = generateUnrelatedIndividuals(sample.size)
gt = retrieveGenotypes(id)
freq = apply(gt,2,sum)/(2*nrow(gt))
causal = sample(setdiff(1:ncol(gt),which(freq==...
2020 Nov 01
0
R: sim1000G
...> vcf = readVCF( vcf_file, maxNumberOfVariants = 442 ,min_maf =
> 0.0005,max_maf = 0.01) #lowest MAF
> dim( vcf$gt1 ) #rows represent number of variants, columns represent
> number of individuals
>
> ## Download and use full chromosome genetic map
> downloadGeneticMap(4)
> readGeneticMap(4)
>
> sample.size=3000
>
> startSimulation(vcf, totalNumberOfIndividuals = sample.size)
>
> data_sim = function(seed.num){
>
> SIM$reset()
>
> id = generateUnrelatedIndividuals(sample.size)
>
> gt = retrieveGenotypes(id)
>
>
> freq = apply(gt,2,...