Genomatics® Product Portfolio
Genomatics builds human-in-the-loop AI products, clinical genomics intelligence tools and curated biomedical knowledge systems that help researchers, diagnostic laboratories and healthcare teams convert genomic evidence into usable insight.
AI-Powered Genomic Intelligence Built on Curated Evidence
Our product journey combines years of scientific curation, bioinformatics workflows and software engineering with responsible AI for clinical evidence navigation, biomedical literature intelligence and variant interpretation support.
GenoMind
Human-in-the-loop genomic intelligence platform
GenoMind is designed as a modern genomic intelligence and workflow platform that brings together clinical data, laboratory processes, curated evidence and AI-assisted interpretation in one connected system.
It supports a practical journey from sample and clinical context to evidence review, bioinformatics interpretation and report generation — with human oversight built into the workflow.
- Integrated workflow across EHR, lab, finance, approvals, bioinformatics and reporting
- Evidence navigation for gene, variant, disease and phenotype relationships
- Human-in-the-loop review for responsible genomic interpretation
- Designed for genomics labs, hospitals, clinicians and precision medicine teams
- Built for usability, governance, compliance and scalable deployment
ChatDiAG
AI-assisted clinical genomics question-answering
ChatDiAG is envisioned as a clinician-friendly AI assistant for genomic and biomedical evidence queries. It helps users ask domain-specific questions and receive structured, evidence-aware responses.
The goal is to reduce the effort required to search literature, interpret variant context and understand gene-disease associations — while keeping expert review at the center.
- Clinical genomics Q&A for doctors, labs and researchers
- Support for variant, gene, disease and phenotype queries
- Designed to work with curated and reference-backed knowledge sources
- Useful for literature review, case discussion and report support
- AI assistance with human validation and responsible use
GERE
AI extraction of genomic entities and relationships
GERE is an AI-assisted literature intelligence tool that extracts structured genomic entities and relationships from biomedical publications.
It helps researchers and curation teams rapidly identify genes, variants, diseases, drugs, phenotypes and evidence relationships from scientific articles.
- Input scientific article PDFs or PMID-based literature
- Extract genes, variants, diseases, drugs and phenotypes
- Identify relationships among extracted biomedical entities
- Generate structured tables and concise article summaries
- Useful for curation, review, research and evidence discovery
VarDiG®-DB
Human-curated genomic variant knowledgebase
VarDiG-DB is Genomatics’ foundational curated variant database, built to capture and organize relationships among genes, variants, diseases, phenotypes, drugs and scientific literature.
Developed through careful manual curation and quality-controlled bioinformatics workflows, VarDiG-DB supports reliable interpretation of clinically and biologically significant variants.
- 6 lakh+ curated biomedical articles / evidence records
- Gene, variant, disease, phenotype and drug associations
- Coverage of SNPs, indels, insertions, deletions and other variant classes
- Publication-linked evidence for research and interpretation workflows
- Built through human curation, software pipelines and stringent quality control
Need a Genomics Intelligence System for Your Lab or Research Team?
Genomatics can help build or customize AI-assisted clinical genomics workflows, literature intelligence tools, curated databases, variant interpretation systems and biomedical knowledge platforms for your organization.
Contact Genomatics