Closed martinghunt closed 6 years ago
Hi,
Thank you for posting!
bayesTyperTools combine
requires the header to contain contig (e.g.##contig=<ID=8,length=146364022>
) entries for all reference sequences containing variants in the vcf; the contigs further need to appear in the same order in the header and for the variant entries. We have added information about this to the readme.
We have not tested BayesTyper on bacteria. There are no theoretical reasons why it shouldn't work, but please note that:
Please do not hesitate to post again if you further questions or suggestions for how we can improve the BayesTyper support for bacterial data.
br,
Lasse
Thank you! I got it working (one of the VCFs didn't have the contig header line)
I got this error message:
Maybe I'm not using it as intended?
My use case is a bacterium where I have calls for one sample from samtools and cortex, not from GATK/playpus/Manta. I don't have the "variation prior", just calls for that sample from samtools and cortex, hence no
prior:<prior>.vcf
in my command line.Can this type of data be used with BayesTyper?