MedGenome, a leading global genomics diagnostics and research company, has partnered with US-based Twist Bioscience to launch the HOPE for Rare Diseases Programme in India. This initiative offers discounted whole exome sequencing to economically disadvantaged patients, marking a milestone in MedGenome’s decade of genomics advancements. The programme aims to democratize access to affordable genetic solutions, addressing the unmet healthcare needs in emerging markets.
Twist Bioscience supports the initiative by providing its advanced Twist Exome 2.0, a tool designed to detect rare diseases and germline cancers. Despite its availability for over a decade, whole exome sequencing has been underutilized due to high costs, limited awareness, and the lack of insurance coverage in India’s out-of-pocket healthcare system. The HOPE Programme, launched in August 2024, seeks to overcome these barriers by offering affordable sequencing for rare disease patients.
Rare genetic diseases, while individually uncommon, collectively affect over 70 million people in India, many of them children. Whole exome sequencing helps clinicians identify genetic variants responsible for these diseases, expediting diagnoses and guiding treatment options, potentially ending patients’ long diagnostic journeys. This partnership aims to make critical genetic information accessible to the underserved, improving care and management.