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Diagnostic Laboratories

Scalable Genomic Interpretation and Reporting for Modern Diagnostic Laboratories

Genix.ai helps diagnostic laboratories operationalize genomic interpretation—improving turnaround time, consistency, and report quality through AI-assisted workflows with full expert oversight.

Clinical genomics platform visualization

The Reality Diagnostic Labs Face

Diagnostic laboratories are under constant pressure to deliver

Genomics workflows
Bioinformatics expertise
Interpretation times
Genomics workflows
Bioinformatics expertise

Faster turnaround times

Clinically reliable interpretation

Consistent report quality across cases

Competitive pricing at scale

Compliance with regulatory and client requirements

How Genix.ai Supports Diagnostic Laboratories

Genix.ai provides labs with a production-ready genomics interpretation platform designed for high-throughput, commercial diagnostic environments.

Standardize interpretation workflows

Reduce manual review burden

Maintain expert control and accountability

Deliver consistent, high-quality reports

Scale services without linear cost increases

key hospital use cases

Clinical Genomic Test Interpretation

Report Generation & Standardization

High-Throughput Operations

White-Label & API-Based Services

How the platform Fits into hospital operations

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Data Integration

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AI-Assisted Interpretation

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Expert Review

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Report Delivery

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Designed For Clinical Trust

Designed For Clinical Trust

Genix.ai is built with hospital realities in mind

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Transparent AI-assisted suggestions

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Clear distinction between AI input and expert judgment

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Consistent interpretation logic across analysts

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Versioned annotations and traceability

Compliance, Security & Client Trust

Diagnostic labs trust Genix.ai because the platform aligns

hospital health

HIPAA-aware data handling

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GDPR-aligned privacy principles

Pharma

Role-based access

Research

Audit trails

Safe and Secure
Public Health

Secure deployment models

Deployment Models for Labs

Labs can choose deployment based on scale and risk profile.

Private VPC

SaaS

Fast onboarding and lower overhead

On-Premise

Private VPC

Preferred for large commercial labs

SaaS

On-Premise

For regulated or sensitive environments

Why Diagnostic Laboratories Choose Genix.ai

Faster interpretation without sacrificing quality

Reduced dependency on scarce expert resources

Consistent, explainable outputs

Enterprise-grade security and governance

Designed for commercial scale

Why hospitals choose Genix.ai

Who Uses The Platform In Labs

Why hospitals choose Genix.ai

Molecular pathologists

Clinical geneticists

Bioinformatics teams

Lab operations managers

Quality and compliance teams

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Frequently Asked Questions

1. Can Genix.ai handle high-throughput NGS data volumes?
Yes. Our cloud-native architecture and automated tertiary analysis pipelines are designed for commercial scale. Whether you are processing 10 samples or 10,000, the platform scales dynamically to ensure turnaround times (TAT) remain consistent without requiring additional in-house bioinformatics headcount.
2. How does the platform assist in reducing manual variant curation time?
Genix.ai automates the "heavy lifting" of evidence aggregation. The AI scans and prioritizes variants using the latest clinical databases (ClinVar, OMIM, gnomAD, etc.) and pre-ranks them based on ACMG/AMP guidelines. This allows your molecular pathologists to focus only on high-relevance variants, reducing manual review time by up to 70%.
3. Does the platform support white-label reporting for our clients?
Absolutely. We offer a fully white-labeled reporting engine. You can customize the visual identity, include your lab’s accreditation logos (e.g., NABL, CAP), and structure the report sections to match your existing clinical templates.
4. How do you handle version control for clinical annotations?
Traceability is core to our platform. Genix.ai maintains versioned annotation trails. Every piece of evidence used to classify a variant is timestamped and archived, allowing your lab to provide a full audit trail for regulatory inspections or retrospective case reviews.
5. Can we integrate our own custom filtering logic or proprietary databases?
Yes. Through our Developer-Friendly API, laboratories can integrate their own internal variant databases or custom filtering "blacklists." This ensures your lab’s unique expertise and historical data are preserved and utilized alongside our global intelligence layers.
6. What is the turnaround time for generating a clinical-grade report?
Once the VCF is uploaded, the AI-assisted prioritization and draft report generation are completed in minutes. The final TAT depends on your internal expert review process, but the platform is designed to eliminate the bioinformatics bottleneck entirely.
7. Is the data storage compliant with laboratory security standards?
Genix.ai employs enterprise-grade security. We use HIPAA-compliant, secure cloud environments with role-based access controls (RBAC). Data is encrypted using AES-256 at rest and TLS 1.2+ in transit, meeting the highest global standards for healthcare data security.
8. Do you offer support for NABL or CAP accreditation documentation?
Yes. We provide technical documentation regarding our bioinformatics pipeline validation, data security protocols, and software versioning policies to assist your quality team during the accreditation process.
CTA Background

Bring Clinical Genomics into Routine Hospital Care

If your hospital or health system is evaluating how to operationalize genomics responsibly and at scale, Genix.ai can support your journey.

Genix.ai - Genomic Precision Wellness
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Genix.ai is an AI-powered clinical platform using NGS and imaging to detect biomarkers early, enabling clinicians to deliver cost-effective, personalized treatments for rare pediatric conditions, cancer care, and infectious diseases.

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Developed in Association with Chadura.