Mimamsia collaborates with patients, patient organizations, the physicians and also clinical labs in improving the diagnostic success of Whole Exome and Whole Genome Sequencing data. Perfect solutions always are a team effort. We strive to find the right solution, through critical analyses, deeper understanding of the emerging information and insightful discussions with our trusted and valuable partners.

PatienTS

If you, anyone in your family or anyone whom you know, are suffering from rare inherited disorders and are still looking for a diagnosis without running into a financial quagmire, we are committed to support you find a solution. We commit that we will never stop until you have a satisfactory understanding of the genetic etiology behind your disease.

PhysicianS

Any negative finding is an equal burden for the treating physician. Physicians having access to datasets that have not been evaluated to new information and approaches in the field find us a valuable partner in digging the past and current data to help solve unsolved cases. Results are only communicated back to the requesting physician.

Clinical Labs

We offer bulk expert analysis of negative large datasets, derived from WES/WGS that have been long buried in your archive. While you focus on new incoming patients, we challenge the old datasets with new advancements in clinical, research and technical areas. All findings are solely communicated to our partners who in turn relay it to their patients. We are transparent in our collaboration with labs to allow improvements in their existing approaches related to variant finding.