Rare & Undiagnosed Network

At Rare Genomics, we are focused on breakthrough discoveries that save lives.

Science 2.0 is an innovative approach to conquering rare diseases that puts patients at the center of finding a cure. It extends beyond genome sequencing to provide a new healthcare delivery model that connects patients with crowdfunding resources and a multi-disciplinary team of world-leading rare disease experts who interpret sequencing results.

Our experts are selected specifically for each patient based on their symptoms.

At Rare Genomics, our mission is to provide diagnoses, treatments and cures for rare disease patients. We search for answers, we provide hope, and we lead healthcare innovation.

Science 2.0: A novel personalized medicine initiative

We recognize that the results of sequencing alone are often not actionable for patients. Science 2.0 takes it a step further. Each patient enrolled in Science 2.0 receives genome sequencing, a personal team of scientific experts dedicated to analyzing their results, and a pro-bono consulting team of world-leading physicians and researchers in rare diseases. Our multi-faceted, patient centered program ensures that every patient with a rare and undiagnosed disease benefits from the latest research. There are six main components:

Crowdfunding

Genome Sequencing

Result Interpretation

Personalized Multi-Disciplinary Medical Team

On-going support

RG Forum

For more information and to enroll, please please Contact Us >

Words cannot express how much we appreciate everything you do for all of the Rare and Undiagnosed families desperately trying to find answers. – Gina

The Szajnuk’s Report:

Szajnuk’s Whole Exome Sequencing (WES) report by the Rare Genomics Institute: Science 2.0