Dear all,
This is my first time using SweeD to look into the selective sweeps, My genome is haploid of 22 individuals and I have a total of 938515 SNPs generated from Freebayes. I have SweeD with default parameters,
./SweeD -name TEST -input /Volumes/sweed/input.vcf -grid 10000
could some one please explain on what basis should i select the #-grid values. my output from the sweed looks wired (or i might have given wrong parameters). please look into the screenshot of my output file from Sweed and H-scan (c++ compiler to detect selective sweep).
My main question is why does my position change into decimals and not specific to the SNPs as in H-scan (where X is position of the SNP and H is the homozigosity value for the specific SNPs)?
I highly appreciate if you could please make to understand the output of SweeD and also choosing the grid values.
Thank you
kind regards
Prakash