My Nonprofit Reviews

Rare Genomics is an elixir for patients with rare diseases. Here volunteers with different specialties are dedicating their valuable knowledge and expertise to respond to patient's query - be it scientific knowledge about the disease concerned, or extra information about patient resources, or high-level sequencing analysis. Here we provide evidence-based supports to patients. One such example is a case where the patient was diagnosed with a particular gene related to his/her disease - we here in RG, provided unique physician information who are directly working on those genes in their laboratory and can give much better support to the patient. Also, we often provide direct clinical trial information, where patients can be benefited. Patients who are requesting for next-generation sequencing analysis, we provide detailed sequence analysis, together with implications of the variants found in the patient's genome or exome. This variant interpretation is very crucial as one can generate a list of variants in an individual's genome, but the proper interpretation/analysis of those data in the context of patient's disease symptoms is rare to get, and there is no cost to get such type of valuable, informative clinical information. In one word, I will highly recommend any patient with the rare disease to approach Rare Genomics for their support in any form with no financial burden.