Description Usage Arguments Value Author(s) Examples
These functions read in all of the individual genotype data files and summarizes the founder allele frequency by sample and SNP.
1 2 3 4 | summarize.genotype.transitions(path = ".", snps)
summarize.by.snps(path = ".", snps)
summarize.by.samples(path = ".", snps)
num.recomb.plot(results, gen)
|
path |
Character, full path to the genotype directory where the *.genotype.probs.Rdata files are stored. |
snps |
Data.frame containing the marker locations. SNP ID, chromosome, Mb anc cM locations in columns 1 through 4, respectively. |
results |
Data.frame containing results as summarized by summarize.genotype.transitions. |
gen |
Numeric vector containing DO outbreeding generation for all samples in results. Must have sample IDs in names. |
Data.frame with six columns: sample, proximal genotype, distal genotype, chr, proximal Mb, distal Mb.
Daniel Gatti
1 | ## Not run: geno.sum = summarize.genotype.transitions()
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