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Leaping towards Precision Genomics:

Precision Insights. Personalized Therapy


 At Galaxi Genomics, we empower physicians with AI-driven genome analysis,
to deliver personalized, evidence-based treatment plans.

Discover Galaxi Genomics Labs

With More than two decades of experience servicing global biotech and pharma leaders, our multidisciplinary team—oncologists, clinicians, and genomic data scientists—transforms complex genomic data into actionable clinical insights.

Why Choose Us?

End-to-End Genomic Analysis

From sequencing to clinically validated reports

Physician-Centric Decision Support

Curated treatment recommendations with scientific backing

Domain-Specialized Expertise

Precision medicine solutions across oncology, Perinatal Health, and rare diseases

More About Us

Our Services

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Solid Tumor Tests

We equip oncologists with cutting-edge genomic profiling to personalize therapy for patients with solid tumors. Our advanced genetic tests detect actionable mutations, fusions, and biomarkers—enabling targeted treatment strategies that drive better outcomes.
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Hereditary Cancer Tests

We offer comprehensive hereditary cancer testing to help oncologists identify patients with inherited cancer risk. Our advanced genomic panels detect germline mutations and assess polygenic risk—empowering early intervention, personalized screening, and prevention.
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Pharmacogenomics Tests

Pharmacogenomics Tests

We empower oncologists to optimize chemotherapy dosing and minimize toxicities through targeted pharmacogenomics testing. By analyzing germline variants in key genes , we guide fluoropyrimidine and irinotecan therapy—enhancing patient safety and treatment efficacy.
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Comprehensive Cancer Profiling

Whole Genome and Whole Exome Tests

Choose the breadth of Whole Genome or the targeted depth of Whole Exome.

We offer both tests to match your clinical needs: Whole Genome for maximum discovery, or Whole Exome for a focused, cost-effective profile.

Blended Genome & Exome (BGE) Sequencing

BGE Sequencing is a sophisticated, single-test approach that combines the comprehensive breadth of Whole Genome Sequencing (WGS) with the ultra-deep, focused coverage of Whole Exome Sequencing (WES)

Why Our Services Matter In Treatment Decisions?

Targeted Therapies,
Better Outcomes
Identify actionable mutations and biomarkers to match patients with the most effective drugs, reducing trial-and-error prescribing.
Uncover Resistance Mechanisms
Detect genetic variants that influence drug response, avoiding ineffective treatments and adverse effects.
Early Risk
Stratification
Proactively assess genetic predispositions to guide preventive care and long-term management.

Change Starts With a Conversation!

Partner with us to bring cutting-edge genomics into your practice—because every patient’s genome holds the key to smarter therapy.

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