I would still be very happy for help. I read again the R-help for loess()
and found the "subset" argument. Might this be a solution?
Thanks
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I have thousands of Fst-values (markers) spread across the genome. I would
like to use Loess to visualize and integrate them along the chromosomes.
This makes sense only along the chromosome, since markers (and thus Fst
values) are physically linked when located in close physical proximity.
The pr
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