Hi all,
I'm stuck with the CLC genomics workbench and I was wondering if anyone could help me.
I'm using CLC to do a SNP analysis. The mapping and SNP calling worked well. To reduce the number of missing information in my data set I want CLC to give me not just the SNPs but also all calls that are homozygous to the reference.
I guess that's possible but I do not find the tool/command for it.
Thanks for any advice!
I'm stuck with the CLC genomics workbench and I was wondering if anyone could help me.
I'm using CLC to do a SNP analysis. The mapping and SNP calling worked well. To reduce the number of missing information in my data set I want CLC to give me not just the SNPs but also all calls that are homozygous to the reference.
I guess that's possible but I do not find the tool/command for it.
Thanks for any advice!
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