This function finds the haplotype region with LOD scores around the given genomic interval.
1 | scan2_snpasso_rng(markers, scan1_output, max_chr, start, end)
|
markers |
A dataframe of marker positions. Should contain a 'chr' and 'pos' column. |
scan1_output |
Output of |
max_chr |
Character value of the chromosome to be plotted. |
start |
Position defining the start of an interval to get scan1 LOD scores.
Should be a single number, and if provided, |
end |
Position defining the end of an interval to get scan1 LOD scores.
Should be a single number, and if provided, |
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