We’re moving the GATK website, docs and forum to a new platform. Read the full story and breakdown of key changes on this blog.
If you happen to see a question you know the answer to, please do chime in and help your fellow community members. We encourage our fourm members to be more involved, jump in and help out your fellow researchers with their questions. GATK forum is a community forum and helping each other with using GATK tools and research is the cornerstone of our success as a genomics research community.We appreciate your help!
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.
We will be out of the office for a Broad Institute event from Dec 10th to Dec 11th 2019. We will be back to monitor the GATK forum on Dec 12th 2019. In the meantime we encourage you to help out other community members with their queries.
Thank you for your patience!
ClipReads tool - only at end of read?
I would like to use the ClipReads tool to soft clip reads (in a bam file) that contain an exact match to a set of sequences (primer seqs). ClipReads should be able to do this, but the problem is with overlapping amplicon regions. with overlapping regions, the primer seq may legitimately appear in the middle of read (as actual sample sequence) and the ClipRead tool will mask it.
Is there a way to instruct ClipReads to only clip reads when a sequence match is found at the END OF READS?