Load overlapping SNP alleles from low-depth sequences of one parent,
you can also use genotype results from traditional genotyping studies,
e.g. results of SSR/RFLP markers.
Usage
data("markerData")
Arguments
Format
The format is:
Named chr [1:272] "G" "T" "A" "C" "G" "C" "A" "T" "A" "C" "T" "A" ...
- attr(*, "names")= chr [1:272] "0500033821G" "0500059721T" "0500125700G" "0500169119C" ...