Genetico Blogs

Insights on rare disease care, genomics, and health infrastructure

Perspectives from clinicians, researchers, and the Genetico team on building diagnostic workflows that scale.

How structured genomic data is reshaping rare disease diagnosis in India

Fragmented records and inconsistent capture slow rare disease diagnosis. Structured genomic workflows are helping referral centers move from suspicion to actionable reports faster.

Arihant Mehra12 June 20266 min read

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Policy

Building national registries: lessons from India's rare disease policy

India's national rare disease framework created momentum. The next challenge is turning policy intent into registries that clinicians, researchers, and public health teams can actually use.

Arjun Gupta28 May 20265 min read

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Research

AI-assisted variant interpretation: what clinicians need to know

AI tools can accelerate variant triage, but clinical teams still need transparency, override paths, and workflow fit. Here is a practical framing for adoption in diagnostic labs.

Dr. Shubha Phadke14 May 20264 min read

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Insights

From phenotype to genotype: closing the diagnostic odyssey

Patients with rare diseases often wait years for answers. Connecting structured phenotyping with genomic testing is one of the most direct ways to shorten that journey.

Dr. Rohit Sadanand30 April 20267 min read

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