Description Usage Arguments Details References Examples
write.ibdhaplo
prepares the marker data file for running IBDHAPLO.
1 2 | write.ibdhaplo(marker, freq, data, member, input.allele = TRUE,
input.haplotype = FALSE, outfile = tempfile("ibdhaplo", fileext = ".txt"))
|
marker |
numeric vector, marker genetic positions in cM. |
freq |
numeric vector, marker reference allele frequencies. |
data |
numeric matrix, genetic marker data. |
member |
string vector, member ID. |
input.allele |
logical, default TRUE. |
input.haplotype |
logical, default FALSE. |
outfile |
string, output file name. |
The input marker data needs to be subject/haplotype by marker/allele. For example, suppose data
is a 4x10 matrix, use input.allele = FALSE
if data
contains counts of reference alleles of 4 individuals at 10 markers; use input.haplotype = TRUE
if data
contains allelic types of 4 haplotypes at 10 markers; use default options if data
contains allelic types of 4 individuals at 5 markers.
MORGAN Tutorial, https://www.stat.washington.edu/thompson/Genepi/MORGAN/Morgan.shtml.
Brown et al. (2012) Genetics 190:1447-1460, https://www.ncbi.nlm.nih.gov/pubmed/22298700.
1 2 3 4 5 6 7 8 9 10 | ## Not run:
nsnp = 7 # number of SNPs
freq = runif(nsnp, 0.05, 0.95)
nhaplo = 4 # number of founder haplotypes
haplotype = sim.haplotype(freq, nhaplo)
marker = sort(runif(7,0,100))
write.ibdhaplo(marker, freq, haplotype, member = c("ind1", "ind2"),
input.haplotype = TRUE)
## End(Not run)
|
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