In order to Expand Genomics Clinical Knowledge we enable the option of sharing knowledge among Franklin's users.
As part of your variant interpretation process, you can select to link a publication, post a note, or share your classification by clicking on the relevant button on the feed.
Everything you share will be displayed to all community members interpreting this variant.
In addition, after classifying a variant you can choose to share the classification with the Franklin community - this will also add your classification to the feed.
All of the linked articles are added to the list in the publication tab, with the 'Panda Paw' community icon.
Still have questions? Reach out to our Support Team, they'll be happy to help!