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Hi,
I am working on whole-genome resequencing dataset of different cultivated (sugar, fodder, leaf and table) and wild beets. I would like to run selective sweep analysis using xpclr. I have already called and filtered my variants and based on the crop types, I have created different vcf files from each crop type. I have some questions regarding the input files for xp-clr, the questions are as follows:
Do I need separate vcf files for each sub-population or simply I could use a vcf file from the whole panel and just use --samples flag for two populations?
Is it necessary to use --rrate flag, since I don't really know the recombination rates?
Meanwhile, i also tried to install xpclr (Chen et al 2010), I am wondering that how can I create hapmapinput files, just to confirm are these files same as the plink output (.geno) files? For example, a vcf file from wild beets is my reference population (hapmapinput1) and from cultivated sugar beets is object population (hapmap2) or vice versa. If so, then may I ask how to create a mapInput file?
Kind regards,
Amar
The text was updated successfully, but these errors were encountered:
Hi,
I am working on whole-genome resequencing dataset of different cultivated (sugar, fodder, leaf and table) and wild beets. I would like to run selective sweep analysis using xpclr. I have already called and filtered my variants and based on the crop types, I have created different vcf files from each crop type. I have some questions regarding the input files for xp-clr, the questions are as follows:
Meanwhile, i also tried to install xpclr (Chen et al 2010), I am wondering that how can I create hapmapinput files, just to confirm are these files same as the plink output (.geno) files? For example, a vcf file from wild beets is my reference population (hapmapinput1) and from cultivated sugar beets is object population (hapmap2) or vice versa. If so, then may I ask how to create a mapInput file?
Kind regards,
Amar
The text was updated successfully, but these errors were encountered: