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variant calling for gbk files?
I just started using me medaka_haploid_variant
to find SNP between ONT reads and HA. I can see that it doesn't work with gbk file (as for e.g. when working with breseq software and Illumina reads). Is this right? and is there an alternative?
Medaka does not support gbk files as input, only fasta. If you wish to annotate the output VCF file you will need to use a standalone program dedicated to that task.