I am a beginner. I know the software is very robust to detect selective sweep, especially with genetic positions in the input file. Now I have a ~100,000,000 SNPs file from whole genome sequence, however the genetic positions of only 50,000 SNPs have been identified by previous studies, moreover the genetic positions are accurate to two decimal places in my organism.
The part of genetic positions is as follows:
my question are whether the genetic positions with the accuracy of two decimal places are suitable for this software, and how to get the genetic positions of the remaining SNPs of not knowing.
Dear hardingnj,
I am a beginner. I know the software is very robust to detect selective sweep, especially with genetic positions in the input file. Now I have a ~100,000,000 SNPs file from whole genome sequence, however the genetic positions of only 50,000 SNPs have been identified by previous studies, moreover the genetic positions are accurate to two decimal places in my organism. The part of genetic positions is as follows:
SNP Chrom Position (pb) Position (cM)
my question are whether the genetic positions with the accuracy of two decimal places are suitable for this software, and how to get the genetic positions of the remaining SNPs of not knowing.
Thank you!