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2.3 years ago
Nemo
•
0
Hello,
I would like to see how many reads I have per variant. Is there any way to get this information using hisat2 or gatk or any other tool?
It's called variant calling. The VCF contains that information. Given your post history it seems you are essentially going blind in your project. I suggest to search for some guided tutorials to get started. The Biostars Handbook would be one option, but it's not entirely free though.
Thanks @ATpoint I have already the variants (vcf format) using gatk haplotypecaller. But I do not see such information like reads per variant in the resulted output file (I see depth of reads and so on but not number of reads per variant). I also looked into biostar handbook the Variant Calling section, and I couldnt find any information related to this.
Number of reads supporting REF & ALT allele: https://gatk.broadinstitute.org/hc/en-us/articles/360037052092-StrandBiasBySample