Hi,
I was having an issue loading all my markers (~6,600) to perform scantwo because it would complain that the vector was too long.
Recently, I realized that the problem was the size of the chromosomes. I am working with Drosophila, chromosome X, 2 and 3. Chromosomes 2 and 3 are subdivided into 2L, 2R, and 3L, 3R for the left and right sides around the centromere. When I treat L and R as separate chromosomes, giving r/qtl 5 chromosome labels instead of 3, scantwo works normally.
Is there a problem with separating the chromosomes into 2 blocks? Does the cM distance between the markers influence their lod scores?
Best,