NGS

  • lab tests dubai

    Comprehensive NGS Colorectal Cancer Panel Test – Accurate Genetic Screening

    4.000,00 د.إ

    The NGS Colorectal Cancer Panel from Lab Tests Dubai is a state-of-the-art genetic test that decodes the unique mutations in your tumor, unlocking critical insights for personalized treatment, targeted therapy selection, and hereditary risk assessment.

  • Mitochondrial DNA Sequencing

    Mitochondrial DNA Sequencing | High-Accuracy mtDNA Analysis for Research & Medicine

    3.750,00 د.إ

    Mitochondrial DNA (mtDNA) Sequencing provides high-resolution analysis of mitochondrial genomes, enabling precise identification of genetic variations. Key features include full-length mtDNA sequencing, high accuracy, and deep coverage, ensuring reliable detection of mutations and heteroplasmy. Benefits include applications in ancestry research, forensic identification, disease association studies, and evolutionary biology.

  • Obesity Health Package

    Oncomine Acute Myeloid Leukemia (AML) Panel – Targeted NGS Solution for AML Research

    5.500,00 د.إ

    The Oncomine Acute Myeloid Leukaemia (AML) Panel is a cutting-edge genetic test that provides a full genomic picture of AML, helping doctors pinpoint key mutations, gene fusions, and copy number changes in genes known to drive the disease. Using advanced next-generation sequencing (NGS), this test delivers fast, precise results, even from limited or degraded sample, so patients get an accurate diagnosis and tailored treatment plans sooner.

  • Obesity Health Package

    Oncomine Myeloproliferative Neoplasm (MPN) Panel – Accurate NGS Testing for MPN Mutations

    5.500,00 د.إ

    The Oncomine Myeloproliferative Neoplasm (MPN) Panel is a cutting-edge genetic test that analyzes key mutations in JAK2, CALR, and MPL, the genes most commonly linked to myeloproliferative disorders. Using advanced next-generation sequencing (NGS), this test provides a highly accurate and efficient way to diagnose and classify MPNs, even when only small or degraded samples are available (as little as 10 ng of DNA or RNA).

  • Obesity Health Package

    Whole Exome Sequencing

    5.375,00 د.إ

    Whole Exome Sequencing (WES) is a powerful genetic testing method that sequences all protein-coding regions (exons) of the genome, covering approximately 1-2% of the DNA where most disease-causing mutations occur. It offers a cost-effective alternative to whole genome sequencing while providing high-depth coverage for accurate variant detection. WES enables the identification of genetic mutations linked to inherited disorders, cancer, and rare diseases, making it a valuable tool for clinical diagnostics, personalized medicine, and research.