Franklin continues to grow and improve with every version. Here are some interesting freshly released features, as well as some general usability updates to make sure our users get the most out of the Franklin Community:

As part of Franklin's commitment to supporting all workflows in the genetic field, we're very excited to announce that we now fully support NGS whole genome low pass sequencing.

In line with this new solution, we have also been working on improving Franklin's ability to call CNVs on whole genome sequencing. Franklin now supports even relatively low mosaics.

We've developed a new way to create and manage your organization's gene panels! In order to improve user experience, we created a better user interface for panel management.
Panels are now located under the Knowledge Base tab - the one place where all your organization's clinical knowledge is centralized. You can easily create a panel and add genes to it.

As always, we’re working to encourage collaboration within the genetics community and generate insights to improve precision medicine worldwide. That’s why Franklin partnered up with two renowned healthcare institutions in Mexico to release the first genomic database to represent exclusively the Mexican population.
This first version of the Mexican database comprises 1.2 million variants from 480 samples provided by INMEGEN and the Institute of Ophthalmology Conde de Valenciana, and can be found on Franklin in the Population Frequencies tool, located on the Variant Assessment application.

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