Hi Everyone
I am new to exome data variant calling. I usually start from a given vcf. I am looking for GATK Pipleine and it has many links, for this link, https://software.broadinstitute.org/gatk/best-practices/workflow?id=11165
and this full one but no code: https://software.broadinstitute.org/gatk/documentation/article.php?id=7870
Is there a link for the complete detailed pipleine with code snapshots and I can't find it?
Thanks
What about this one?
I added it above, its doing some test, assuming you have your bams, and doesn't show base recabiliaration code and various steps. I have the pipeline for RNAseq variant calling GATK, i starts from raw reads and give steps till the end, can't find similar one for exome data. Thanks,