Closed annarerra closed 2 years ago
I'm not sure exactly what you mean, but I don't think so. If you are using a VCF, the ID in the output should include contig and position in the output?
For the unitigs for example, after annotation for every unitig we have a colomn with this contig:position;upstream;in;downstream info.
But for SNPs there is no such an "annotation" step and we have only these info:
What data and file are you using as input? What command are you running here?
input: phenotypes + gene presence absence from roary + model command: pyseer --lmm --phenotypes {input.pheno} --pres {input.presence} --load-lmm {input.model} --cpu {threads} --output-patterns {output.patterns} --min-af 0.02 --max-af 0.98 > {output.results}
So these are genes then, not SNPs?
yeah, u are right, i am sorry i had genes in mind and i was talking about SNPs :/
but still my question is about the position.
For example if i want to do a manhattan plot, not using phandango, i would need some positions in the genome, or in a contig. Probably is not provided by pyseer, i should do it externaly.
Hello,
there is a way to "map" or "annotate" the snps provided by pyseer in terms of position in the different contigs as it is done for the unitigs?
Thank you in advance :)