Fragmented Genetic Data
Lab reports, phenotype notes, HPO terms, and family histories exist in disconnected silos — making a unified clinical picture difficult to assemble quickly.
Meet us at SALDS’26 – Bangalore
AI-Enabled Clinical Platform for Rare & Genetic Diseases
Designed for clinical geneticists. Built for real-world workflows.
Asia’s first and leading platform unifying case management, variant interpretation, and structured clinical reporting — under clinician supervision.
The Clinical Reality
Genetic Diagnostics is Complex.
Your Workflow Shouldn’t Be.
We understand what it takes to run a clinical genetics practice. The fragmentation, the manual load, the delay between sequencing and report — Genetico was designed in response to exactly this reality.
Manual Variant Interpretation Burden
Classifying variants against ACMG criteria, cross-referencing databases, and synthesising literature is time-intensive without structured support.
Reporting Delays
The time between completing interpretation and delivering a structured clinical report adds unnecessary burden for patients and families awaiting results.
No Integrated Workflow
Clinical teams navigate disconnected tools — VCF viewers, phenotyping platforms, report editors — with no coherent thread from case intake to final output.
The Platform
A Unified Clinical Platform
Four integrated pillars — each purpose-designed for the clinical geneticist’s day-to-day reality, connected within a single cohesive environment.
01
Case Management
Structured end-to-end case tracking — from referral and phenotype capture through investigation ordering and result receipt. Organise patient data, family pedigrees, and clinical history within a single longitudinal case record.
Pedigree IntegrationHPO PhenotypingMulti-proband FamiliesTimeline View
02
Variant Interpretation Support
A structured interpretation workspace aligned to ACMG/AMP 2015 guidelines. Criteria-based evidence review, population frequency integration, in-silico tool aggregation, and auditable decision records — all clinician-led.
ACMG Criteria MappingClinVar / gnomADIn-silico AggregationAudit Trail
03
Structured Clinical Reporting
Generate complete, structured, institution-branded clinical reports directly from interpretation data. Customisable templates for WES, WGS, gene panels, and chromosomal microarray — with minimal manual reformatting.
Report TemplatesAuto-populationVariant NarrativeSignoff Workflow
04
AI-Assisted Insights
Carefully scoped AI functions that assist — not override — clinical judgement. Phenotype-driven differential prioritisation, relevant literature surfacing, and pattern-based triage suggestions, presented transparently with full clinician control.
Differential PrioritisationLiterature SurfacingTriage AssistClinician Override
Our Philosophy
AI That Assists.
Not Overrides.
We believe that in clinical genetics, the clinician’s judgement is non-negotiable. Genetico’s AI functions are designed to reduce cognitive load, surface relevant data, and support decision-making — never to substitute it.
Assists in Case Triage
AI surfaces cases that may warrant clinical priority based on phenotypic patterns, without suppressing any case from view.
Supports Variant Interpretation
Structured evidence is organised and presented — but criteria assignment and final classification remain entirely with the clinician.
Surfaces Relevant Literature
Phenotype and gene-matched literature is surfaced contextually within the interpretation workspace, reducing manual search time.
Always Under Clinician Supervision
Every AI output is labelled, transparent, and overridable. The system augments clinical expertise — it does not operate outside it.
Trust & Credibility
Built to Be Trusted
Genetico is the result of deep clinical collaboration, multidisciplinary expertise, and a commitment to clinically mature, responsible design.
Trusted by Leading Clinical Institutions
Adopted at tertiary care and academic medical centres across India. [Institution names — placeholder.]
Government-Backed Innovation
Supported by national innovation programmes and recognised under India’s digital health and MedTech development initiatives. [Programme names — placeholder.]
Multidisciplinary Expert Team
Developed with clinical geneticists, molecular biologists, bioinformaticians, and healthcare experience designers working in close collaboration.
Find Us at the Event
Visit Us at the Booth
We’d welcome a conversation with you in person. Come see Genetico in the context of your clinical workflow — no sales deck, just a real product walkthrough.
What you’ll see at our booth
Live Workflow Walkthrough — See the complete journey from case intake and HPO phenotyping through to variant interpretation and structured report generation.
AI in Action — Watch how Genetico’s assistive AI surfaces differentials, populates ACMG evidence, and highlights literature — with full clinician control throughout.
Real Clinical Use Cases — Demonstrations drawn from rare disease presentations — paediatric metabolic, cardiogenetics, skeletal dysplasias — to show platform depth in context.
One-to-One Conversations — Our team includes clinical geneticists and bioinformaticians. Bring your questions about workflows, fit, or specific clinical scenarios.
Request a Demo
See Genetico in Your Clinical Context
Whether at the booth or at a time convenient to you — we’d welcome the opportunity to walk you through the platform in the context of your own practice or institution.
Tailored to your specialty — We adapt demonstrations to cardiogenetics, metabolic, paediatric genetics, or your specific area.
No obligation — This is a clinical conversation, not a sales interaction.
Speak to the team directly — Our demonstrations are led by people with clinical genetics and bioinformatics backgrounds.
Request a Demo
Complete the form and our team will be in touch within 24 hours.
Genetico
Built for the Future
of Clinical Genetics.
Asia’s first AI-enabled clinical platform for rare and genetic diseases — matured through real clinical collaboration, and ready for your practice.