I've been following the guide on the Tracy website for looking at variants in some Sanger sequences I have:
https://www.gear-genomics.com/docs/tracy/cli/#variant-calling
I've now generated the bcf files, and it says I can convert these to vcf using bcftools. How do I do this? I checked the bcftools manual, and there's a general guide to each of the commands, but it's still not clear what I actually need to write to make a vcf from my bcf file, and I can't find a clear explanation online either.
I tried the following:
bcftools convert -O v -o outfilename.vcf inputfilename.bcf
Which gave me a file with .vcf at the end but IGV isn't able to read it. I also tried using igvtools to generate an index file (which it did), but still IGV gives me "error loading outputfilename.vcf null" and doesn't show anything on the track.
Thanks in advance
So if I understand correctly replacing the 'z' with a 'b' changes the output file from a compressed VCF, to a compressed BCF?
Yes exactly.