than you for this workflow ! I successfully ran it for 2000WGS ! However, I got a 'too many files open' for VCF_MERGE and I add to modify the 'script' section run bcftools merge by batch of 100 files.
The HTML output is really nice but as a bioinformatician it is less useful. I'd like to see the merge VCF file in the final output as well as a TSV file containing the haplogroups, the contamination status for each sample, etc....
Furthermore, in the VCF file, it would be useful to get the annotations (Expected,Local-Private, etc...) in the INFO/FORMAT .
Hi,
than you for this workflow ! I successfully ran it for 2000WGS ! However, I got a 'too many files open' for VCF_MERGE and I add to modify the 'script' section run
bcftools merge
by batch of 100 files.The HTML output is really nice but as a bioinformatician it is less useful. I'd like to see the merge VCF file in the final output as well as a TSV file containing the haplogroups, the contamination status for each sample, etc....
Furthermore, in the VCF file, it would be useful to get the annotations (Expected,Local-Private, etc...) in the INFO/FORMAT .
Thanks !