ONCO CREAT™ – Whole Genome Sequencing
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ONCO CREAT™ – Whole Genome Sequencing is an advanced genomic diagnostic solution designed to analyze the complete DNA sequence of an individual’s genome. This cutting-edge technology helps identify genetic variations, mutations, and biomarkers associated with cancer risk, progression, and treatment response. By decoding the entire genome, ONCO CREAT™ provides clinicians with powerful insights to support precision oncology and personalized treatment strategies.
Whole Genome Sequencing (WGS) enables comprehensive detection of genetic alterations including single nucleotide variants (SNVs), insertions and deletions (Indels), structural variations, and copy number changes. This extensive analysis empowers healthcare professionals to better understand tumor biology and guide targeted therapy decisions.
Key Benefits
✔ Comprehensive analysis of the entire genome
✔ Detects cancer-related mutations and genetic variants
✔ Supports personalized oncology treatment planning
✔ Enables early detection of hereditary cancer risks
✔ Provides actionable genomic insights for clinicians
Technology Highlights
• Advanced Next-Generation Sequencing (NGS) platform
• High-resolution genomic analysis
• Detection of SNVs, CNVs, Indels, and structural variants
• Deep sequencing coverage for accurate results
• Clinically relevant genomic interpretation
Usage / Sample Requirements
• Blood sample or tissue biopsy (as recommended by physician)
• Sample processed in certified molecular diagnostic laboratory
• Results interpreted by genomic specialists and oncologists
Ideal For
• Cancer diagnosis and molecular profiling
• Precision oncology treatment selection
• Hereditary cancer risk assessment
• Advanced clinical research and genomic studies
What You Receive
• Comprehensive Whole Genome Sequencing report
• Detailed mutation analysis
• Clinical interpretation of key genetic variants
• Actionable insights for personalized treatment decisions
Safety & Care
This genomic test should be performed under medical supervision. Results must be interpreted by qualified healthcare professionals or genetic specialists.
Free From
• Limited gene panel restrictions
• Partial genomic analysis
• Incomplete mutation detection
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#WholeGenomeSequencing #PrecisionOncology #Genomics #CancerGenetics #NGSDiagnostics #MolecularDiagnostics #AdvancedBiocare #GeneticTesting #OncologyTesting #ourdermastore
