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.
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.
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.
Lab reports, phenotype notes, HPO terms, and family histories exist in disconnected silos — making a unified clinical picture difficult to assemble quickly.
Classifying variants against ACMG criteria, cross-referencing databases, and synthesising literature is a time-intensive process when performed without structured support.
The time between completing interpretation and delivering a structured clinical report adds unnecessary burden — and uncertainty — for patients and their families awaiting results.
Clinical teams navigate multiple tools — VCF viewers, phenotyping platforms, report editors — with no coherent thread connecting case intake to final clinical output.
Four integrated pillars — each purpose-designed for the clinical geneticist’s day-to-day reality, connected within a single cohesive environment.
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.
A structured interpretation workspace aligned to ACMG/AMP 2015 guidelines. Criteria-based evidence review, population frequency integration, in-silico tool aggregation, and auditiable decision records — all clinician-led.
Generate complete, structured, institution-branded clinical reports directly from interpretation data. Customisable templates for different assay types — WES, WGS, gene panels, chromosomal microarray — with minimal manual reformatting required.
Carefully scoped AI functions that assist — not override — clinical judgement. Phenotype-driven differential prioritisation, relevant literature surfacing, and pattern-based triage suggestions are presented transparently, with full clinician control at every step.
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.
AI surfaces cases that may warrant clinical priority based on phenotypic patterns, without suppressing visibility of any case.
Structured evidence is organised and presented — but criteria assignment and final classification remain entirely with the clinician.
Phenotype and gene-matched literature is surfaced contextually within the interpretation workspace, reducing manual search time.
Every AI output is labelled, transparent, and overridable. The system is designed to augment clinical expertise — not operate outside it.
Genetico is the result of deep clinical collaboration, multidisciplinary expertise, and a commitment to clinically mature, responsible design.
Adopted at tertiary care and academic medical centres across India. [Institution logos / names placeholder — to be provided by the Genetico team.]
Supported by national innovation programmes and recognised under India’s digital health and MedTech development initiatives. [Specific programme names — placeholder.]
Developed with clinical geneticists, molecular biologists, bioinformaticians, and healthcare experience designers — not software engineers working in isolation from clinical reality.
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 relevant literature — with full clinician control throughout.
Real Clinical Use Cases — Demonstrations drawn from actual 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, institutional fit, or specific clinical scenarios.
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 of practice.
No obligation — This is a clinical conversation, not a sales interaction. We’ll be honest about fit and limitations.
Speak to the team directly — Our demonstrations are conducted by people with clinical genetics and bioinformatics backgrounds.
Complete the form and our team will be in touch within 24 hours.
Asia’s first AI-enabled clinical platform for rare and genetic diseases — matured through real clinical collaboration, and ready for your practice.