Thank you very much for the development of this tool!
I saw in the README that it is possible to call variants in non-diploid organisms.
Is this meant for polyploid genomes? And in what way does it differ with the diploid variant calling? I do not seem to find anything about it in the publication and I would like to use Clair3 for tetraploid data. Many thanks in advance.
Hello,
Thank you very much for the development of this tool! I saw in the README that it is possible to call variants in non-diploid organisms. Is this meant for polyploid genomes? And in what way does it differ with the diploid variant calling? I do not seem to find anything about it in the publication and I would like to use Clair3 for tetraploid data. Many thanks in advance.