Clinical insights, updates, and learning from Genetico
A curated collection of videos, articles, and clinical updates from Genetico's work in rare and genetic diseases. Built for clinicians, researchers, and healthcare teams.
How AI is helping identify rare diseases: Arjun Gupta on The Startup Show
Genetico founder Arjun Gupta joins Amar Ujala's The Startup Show to talk about how AI can help clinicians recognise and diagnose rare diseases. The episode also looks at India's startup ecosystem and the Delhi Startup Policy 2025. In Hindi.
Short walkthroughs
Under ten minutes each — how the workflow actually runs.
The Genetico solution, in our founder's words
Arjun Gupta traces how India's rare disease policy has changed over the years, where implementation still falls short, and how Genetico works across the ecosystem, including the opportunity for pharma.
The Startup Show: Genetico in two minutes
Highlights from Arjun Gupta's interview on Amar Ujala's The Startup Show, on how AI is helping identify rare diseases. In Hindi.
Feature-length sessions
Full panels and conference recordings, unedited.
The missing digital layer in rare diseases
At the IHW Council's Rare Disease Action Summit, Arjun Gupta explains why rare disease care still runs on manual, fragmented processes, and how structured data, AI-assisted decision support and longitudinal patient records can change that. The audio is clearest from 5:03 to 9:35.
Rare Disease Action Summit · IHW CouncilWhy genomic EMRs matter: insights from SIAMG 2025
Dr. Shubha Phadke on why India needs structured, interoperable genomic medical records, and Dr. Neerja of AIIMS Delhi on a year of using Genetico in clinical practice.
SIAMG 2025Positions and commentary
Where Indian rare disease policy and practice actually stand.
From the team
See all →Notes from the clinicians and engineers building the platform.
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.
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.
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.
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.
One reading list, every week
Approvals, papers and guidance in rare and genetic diseases, each with a short note on why it matters. Every past edition is archived and searchable.