Hi Karl,
I'm get an error message running a binary scan in QTL2, and the output looks a little odd.
2: In scan_binary_onechr(genoprobs, pheno, addcovar, maxit, tol, qr_tol, :
binreg didn't converge

If I use the default model (obviously inappropriately, because it's a binary trait), I don't get quite such dramatic pits or the "didn't converge" error message (see below). Changing maxit doesn't seem to help.
For a little more context: this is a map from a non-model system (Rumex) with very unevenly distributed recombination (mostly at the tips of chromosomes). This is simply a scan to confirm the identity of the sex chromosome by localizing sex as a phenotype; multiple other sources of data (e.g. GWAS from a population, distribution of XY polymorphisms in a pedigree cross, etc.) localize the sex-linked region to the same part of the chromosome. There are almost certainly errors in our assembly (the genome is highly repetitive) and in our map (because there is very, very low recombination across most of the chromosome - about 3/4 of the physical map is actually localized at above 60cm).
Do you have any thoughts about what those dips are? I'm assuming they're picking up on errors in our assembly or map. And should we worry too much about the converging? This is mostly just another way to localize something we already know.
Thanks!
Joanna