GO Pathology Workbench by GenomOncology is an end-to-end solution that integrates directly with lab sequencers, annotates detected variants, matches patients to clinical trials, provides data on recommended and adverse therapies, and produces a comprehensive summary report.
As a GO Pathology Workbench user, you can preview the number of published articles related to each variant directly within the Potential Significance tab, and then click the pre-populated Mastermind link to view the evidence in Mastermind.
Here’s how you can view Mastermind results from GO Pathology Workbench:
After logging into GO Pathology Workbench, either click “See More Information” or “View Details and Edit.” for your Variant of interest.
At the bottom of the “More Information” pop-up screen, click the Mastermind “view” link next to the article number to view the articles citing the variant in Mastermind.
Alternatively, on the “View Details and Edit” page, click the Mastermind “view” link next to the article number to view the articles citing the variant in Mastermind.
View the list of publications in Mastermind.
Click an article to view the reference to the variant in context.
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See all of the trusted variant interpretation solutions that Mastermind is integrated with.