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I'm finding the tool works really well and much better than other tools. I have a question about where to find the phased variants in the output. I can see that whatshap is run on my human sample and there are many split-by-chromosome files in /tmp/phase_output/phase_bam and /tmp/phase_output/phase_vcf. However, my final merge_output.vcf.gz doesn't appear to contain any phased variants.
I am running a GM24385 30X bam file with the following command:
Clair3 doesn't provide phased variant output. But we have received many requests in the past months for providing phased variant output. Thus we are preparing a new release (release 8) that allows users to use whatshap to phase the variant calls for output. We will release the new version late this week, stay tuned.
Hi folks,
I'm finding the tool works really well and much better than other tools. I have a question about where to find the phased variants in the output. I can see that whatshap is run on my human sample and there are many split-by-chromosome files in
/tmp/phase_output/phase_bam
and/tmp/phase_output/phase_vcf
. However, my finalmerge_output.vcf.gz
doesn't appear to contain any phased variants.I am running a GM24385 30X bam file with the following command:
Where should I be looking for the final phased results?
thanks
Richard
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