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I have a problem about the input file. I have a vcf file containing 420 samples with a reference genome of ~400m bps. For some loci, different samples may have different alleles, e.g., "C,T" in the ALT column. I found that these loci were filtered out in the HeaderCheckFailed category.
If I'm confident in these alleles, is it possbile to include these loci? Or maybe I'm doing something wrong? I really appreciate your help. Thank you!
The text was updated successfully, but these errors were encountered:
On Wed, Apr 3, 2024 at 4:38 AM carolynzy ***@***.***> wrote:
Hi, thanks for developing this useful software!
I have a problem about the input file. I have a vcf file containing 420 samples with a reference genome of ~400m bps. For some loci, different samples may have different alleles, e.g., "C,T" in the ALT column. I found that these loci were filtered out in the HeaderCheckFailed category.
If I'm confident in these alleles, is it possbile to include these loci? Or maybe I'm doing something wrong? I really appreciate your help. Thank you!
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Hi, thanks for developing this useful software!
I have a problem about the input file. I have a vcf file containing 420 samples with a reference genome of ~400m bps. For some loci, different samples may have different alleles, e.g., "C,T" in the ALT column. I found that these loci were filtered out in the HeaderCheckFailed category.
If I'm confident in these alleles, is it possbile to include these loci? Or maybe I'm doing something wrong? I really appreciate your help. Thank you!
The text was updated successfully, but these errors were encountered: