Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

GATK process banner

Need Help?

Search our documentation

Community Forum

Hi, How can we help?

Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

Add samples to CNV analysis without re-running all samples?

0

1 comment

  • Avatar
    Gökalp Çelik

    Hi Joel Wallenius

    Yes you can do it. Actually we have a case mode available for the GCNV workflow which uses a model created using the cohort mode and generates the same segmented CNV calls for your additional files. Since the model is created already case mode runs quite fast. 

    I hope this helps.

    Regards. 

    0
    Comment actions Permalink

Please sign in to leave a comment.

Powered by Zendesk