Back to resources

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.

Clinical

Clinical

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 Mehra2026-06-11T18:30:00.000Z6 min read
Read blog
Policy

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 Gupta2026-05-27T18:30:00.000Z5 min read
Read blog
Research

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 Phadke2026-05-13T18:30:00.000Z4 min read
Read blog
Insights

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 Sadanand2026-04-29T18:30:00.000Z7 min read
Read blog