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

After gCNV calling considerations Follow

2 comments

  • Avatar
    Seunghun Han

    Hi,

    the notebook links in "2. Towards ascertaining the quality of gCNV calls, use Jupyter Notebook" section seem to have been broken. Is there a way to access these notebooks? 

     

    1
    Comment actions Permalink
  • Avatar
    James Mills

    Hi,

    Yes, is there any update on Seunghun Han's reqeust?

    Kind regards,

    James

    1
    Comment actions Permalink

Please sign in to leave a comment.

Powered by Zendesk