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First of all, thanks for this amazing tool. Not only, it is fast but is structured so well that it is a joy to use.
This is from your comment in anchorwave repo. I have multiple pairwise MAF files (generated by anchorwave) for a common reference and multiple query genomes. I was wondering about the way to convert this into a multi genome MAF, based on the common reference genome.
This would be of great help to me as I can then use wgatools to call a multi sample VCF.
Thanks Again!
The text was updated successfully, but these errors were encountered:
About converting multiple individual MAF alignments into ONE MAF, pafpseudo subcommand could generate pesudo-maf file from multiple query alignment PAF files based on a reference. But the reason it's called pesudo-maf is that this step ignores the insertion information.
About multi-sample vcf, I actually did consider the possibility of providing gvcf result for individuals to provide multi-sample joint-calling. But this is just an idea in my brain, it doesn't produce any line of code yet, oops 🙃
If you have any idea about this, please let me know :)
Hi,
First of all, thanks for this amazing tool. Not only, it is fast but is structured so well that it is a joy to use.
This is from your comment in anchorwave repo. I have multiple pairwise MAF files (generated by anchorwave) for a common reference and multiple query genomes. I was wondering about the way to convert this into a multi genome MAF, based on the common reference genome.
This would be of great help to me as I can then use wgatools to call a multi sample VCF.
Thanks Again!
The text was updated successfully, but these errors were encountered: