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I'm trying to run demuxlet with 8 individuals, and I always get a lot of doublet calls, but strangely not many AMB calls. I saw the discussions in previous issues here and here, and I tried the following parameter settings, but couldn't solve my problem.
I was getting 470/4927/4603 AMB/DBL/SNG calls in the first setting, and 435/6004/3561 AMB/DBL/SNG in the second setting.
I see that in my .best file, N.SNP and RD.UNIQ is smaller than the example file you gave here. Not sure if this could cause any problem or not. See the histogram below:
If the small N.SNP and RD.UNIQ is the problem, how can I fix it? The vcf file I'm using is from SNPs array data, and the RD.TOTL seems fine (see below). So it's not the problem of SNPs. Is it because of any read filtering steps? Do you have any suggestions?
The text was updated successfully, but these errors were encountered:
Do you think it could be due to the read filtering steps? Because I feel the RD.TOTL is comparable. Is there a way to know if the SNPs give enough power or not, and how good the estimation is?
I'm trying to run demuxlet with 8 individuals, and I always get a lot of doublet calls, but strangely not many AMB calls. I saw the discussions in previous issues here and here, and I tried the following parameter settings, but couldn't solve my problem.
I was getting 470/4927/4603 AMB/DBL/SNG calls in the first setting, and 435/6004/3561 AMB/DBL/SNG in the second setting.
I see that in my .best file, N.SNP and RD.UNIQ is smaller than the example file you gave here. Not sure if this could cause any problem or not. See the histogram below:
If the small N.SNP and RD.UNIQ is the problem, how can I fix it? The vcf file I'm using is from SNPs array data, and the RD.TOTL seems fine (see below). So it's not the problem of SNPs. Is it because of any read filtering steps? Do you have any suggestions?
The text was updated successfully, but these errors were encountered: