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 AIIMS Delhi reduced rare disease diagnosis time from 3 weeks to 4 days
A documentary-style look at how structured genomic workflows and cross-department collaboration transformed rare disease diagnosis at one of India's largest referral hospitals.
Short walkthroughs
Under ten minutes each — how the workflow actually runs.
AI Variant Calling: A 5-Minute Clinical Walkthrough
A concise walkthrough of how AI-assisted variant calling supports faster, more consistent interpretation in clinical genomic workflows.
From Sample to Report: Streamlining Rare Disease Workflows
See how integrated sample tracking, analysis, and reporting reduce handoffs across multidisciplinary rare disease teams.
Genetico Platform Overview for Diagnostic Labs
An introduction to the core modules labs use to manage cases, collaborate on interpretation, and deliver actionable genomic reports.
Feature-length sessions
Full panels and conference recordings, unedited.
Building National Genomics Infrastructure: Summit Panel Discussion
Keynote and Q&A on policy frameworks, technology stack, and cross-institutional data sharing for LMICs.
Global Rare Disease Summit · GenevaRare Disease Care in India: Conversation with Leading Geneticists
Panel discussion on rare disease burden, registry development, and AI-assisted clinical tools across five Indian states.
ISHG Annual ConferencePositions 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.
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