Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN)
GUaRDIAN is a collaborative research programme towards understanding the genetic basis and molecular mechanisms underlying rare genetic disorders. We use the advanced sequencing technologies, extensive bioinformatics and animal models. Our collaborators include a large number of clinicians and scientists. [more]

BENCH TO BEDSIDE FOR MITOCHONDRIAL DISEASES

April 2016
: The know-how for mitochondrial sequence analysis has been transferred to Eurofins Clinical Genetics India Ltd (Subsidiary of Eurofins Scientific, a world leader in testing services). The product is available in the Indian market.

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CSIR Institute of Genomics and Integrative Biology (CSIR-IGIB) with its rich expertise in the area of genomics and a wide network of clinical partners across the country has embarked on a unique outreach programme, to enable equitable access to genetic testing for frequent genetic diseases. This programme aims to provide a platform for clinicians to tap into the rich and varied expertise of CSIR-IGIB in disease genomics to solve clinical problems.[more]

Omics for Precise Therapeutic Interventions Minimising Adverse Events (OPTIMA) is a research collaboration aimed at pioneering Precision Medicine in India through enabling genomic understanding of sub-optimal therapeutic response. [more]