We like to think that Franklin is built for the community and by the community, so we encourage our community members to share their insights and Expand Genomics Clinical Knowledge - Together!

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 future 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.