chr17:7,676,154 · TP53 · pipeline LIVE

AI-powered precision medicine

Clinical Genomics & Multi-Omics Intelligence

Tribro-Omics turns raw sequence into clinical answers — an end-to-end platform spanning sequencing, multi-omics integration and AI interpretation, from sample to signed report.

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Tribr mics
DECODING BIOLOGY · END TO END

Our services

End-to-end genomic medicine

From sequencing to clinical interpretation — six service lines covering the full precision-medicine workflow.

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Whole Genome Sequencing

Comprehensive genomic analysis providing complete DNA sequencing for clinical and research applications with the highest accuracy.

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Clinical Diagnostics

Advanced diagnostic testing for genetic disorders, rare diseases and personalized treatment recommendations.

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Bioinformatics Analysis

State-of-the-art computational analysis and interpretation of genomic data using AI and machine learning.

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Pharmacogenomics

Personalized drug-response prediction based on genetic makeup to optimize therapeutic outcomes.

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Cancer Genomics

Comprehensive tumor profiling and liquid-biopsy solutions for precision oncology applications.

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Reproductive Health

Preconception screening, prenatal testing and newborn genetic screening services.

Our products

The Tribro product suite

Modular, clinical-grade products for sequencing, interpretation and reporting.

WGSTribro

Whole Genome Sequencing solution providing comprehensive genomic analysis with advanced variant detection and clinical interpretation.

  • 30X coverage genome sequencing
  • SNV, CNV and SV detection
  • Clinical-grade reporting
  • Pharmacogenomic insights
  • Ancestry analysis
WESTribro

Whole Exome Sequencing focusing on protein-coding regions for cost-effective diagnostic testing and rare-disease identification.

  • Clinical exome sequencing
  • Rare variant prioritization
  • Trio analysis available
  • ACMG guidelines compliance
  • Genetic counseling support
PANELTribro

Targeted gene-panel testing for specific clinical conditions with focused analysis and rapid turnaround times.

  • Customizable gene panels
  • Disease-specific testing
  • High-depth coverage
  • Rapid reporting
  • Cost-effective solution
VARIANTTribro

Advanced variant analysis and interpretation platform using AI-powered algorithms for accurate clinical reporting.

  • AI-powered variant calling
  • Population database integration
  • Clinical significance scoring
  • Automated reporting
  • Quality control metrics
RNASEQTribro

RNA sequencing analysis for gene-expression profiling, transcript analysis and functional genomics research.

  • Bulk and single-cell RNA-seq
  • Differential expression analysis
  • Pathway enrichment
  • Splice variant detection
  • Fusion gene identification
Challenge Card

NEGATIVE report → Tribro-Omics POSITIVE report

We challenge ourselves and invite customers to share their negative reports and associated data — we will work to solve your case.

— Tribro-Omics team

Submit your case →

End-to-end solution

Watch a case run, sample to report

PIPELINE RUNNING · case TBO-2026-0417
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Sample Intake

Blood, tissue, FFPE or cfDNA accessioned & QC'd

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Library & Sequencing

NGS library prep and high-depth sequencing

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QC & Alignment

Quality control and reference alignment

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Variant Calling

SNV, CNV and structural variant detection

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AI Interpretation

Prioritization, ACMG classification, literature

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Clinical Report

Structured, reviewable report for sign-out

[INTAKE]Initializing pipeline…

Multi-omics platform

One knowledge engine, every layer of biology

Eight omics layers — genome to proteome — are stacked and read together, each feeding a single AI knowledge engine that integrates the signals into one interpretation.

AI ENGINE

Disease areas

Depth where it matters clinically

Oncology

Solid & rare tumors

  • Glioblastoma (GBM)
  • Breast cancer
  • Lung cancer
  • Colorectal cancer
  • Pancreatic cancer
Rare disorders

Undiagnosed disease

  • Neurological
  • Mitochondrial
  • Developmental
  • Inherited syndromes
Neurology

Neurogenetics

  • Epilepsy
  • ALS
  • Parkinson's
  • Alzheimer's
  • Autism
Cardiovascular

Inherited cardiac

  • Cardiomyopathy
  • Arrhythmias
  • Aortopathy

AI clinical intelligence

The interpretation layer that sets us apart

A knowledge-graph engine that prioritises variants, applies guidelines and drafts the clinical narrative.

01

AI Variant Prioritization

Ranks candidate variants by pathogenicity, gene–phenotype fit and inheritance.

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ACMG Classification Engine

Applies ACMG/AMP criteria with transparent, evidence-linked scoring.

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HPO-driven Diagnosis

Matches phenotype terms to candidate genes to focus the search.

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Literature Mining

Surfaces supporting evidence from the published record at scale.

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Drug Repurposing

Connects molecular findings to existing and investigational therapies.

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Clinical Report Generation

Drafts structured, reviewable reports for sign-out by clinical experts.

Why Tribro-Omics

Built as a platform, not a service desk

CapabilityTypical providerTribro-Omics
Clinical genomicsLimitedYes
AI interpretationLimitedYes
Multi-omicsPartialIntegrated
Single-cellLimitedYes
ProteogenomicsRareYes
Rare diseaseLimitedYes
Precision oncologyPartialComprehensive

Research output

Lead Publications

Peer-reviewed work where Kumar, A. is first or senior (last) author. Titles link to Google Scholar. The complete bibliography is on the Published Articles page.

Submit a project

Detailed sample & analysis request

Tell us about your samples and goals. We'll scope turnaround, coverage and reporting and reply with a tailored plan.

Get in touch

Talk to our genomics team

Questions about diagnostics, collaboration or a quick scoping call — we reply within one business day.

Send a message

For general enquiries, partnerships and clinical questions.

✉️
Email
info@tribro-omics.com
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WhatsApp
+91 86603 08678
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Web
tribro-omics.com
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Hours
Mon–Fri · 09:00–18:00