Test-drive the GATK tools and Best Practices pipelines on Terra
Check out this blog post to learn how you can get started with GATK and try out the pipelines in preconfigured workspaces (with a user-friendly interface!) without having to install anything.
merge the output from SVgenotyper of genomestrip
I am running genometrip on genome sequencing data. i have 8 different varieties and i want to run genome strip for each species individually. after running the SVgenotype i got vcf file. Now, can i merge vcf from eight varieties and then run cnvdiscovery ?? Is this good way to identify deletion ??
Thanks in advance