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3.500,00 د.إThe 24G Pharmacogenomics plus DNA Test is a cutting-edge genetic analysis that provides personalized insights into drug response and overall health. It examines pharmacogenomics, helping to predict how your body metabolizes medications, reducing adverse drug reactions and optimizing treatment plans. Additionally, it includes a comprehensive DNA test covering traits, wellness, and genetic predispositions. Key benefits include personalized medication guidance, enhanced treatment safety, and actionable health insights.
Sample Type : Saliva
Methodology : Illumina
TAT : 3-6 Weeks
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4.000,00 د.إNGS Colorectal Cancer Panel Test – Comprehensive Genetic Profiling for Precision Oncology The NGS Colorectal Cancer Panel Test from Lab Tests Dubai is a cutting-edge, next-generation sequencing (NGS) diagnostic tool that analyzes the genetic makeup of colorectal tumors to guide precision treatment, predict drug response, and identify hereditary cancer syndromes like Lynch syndrome. This advanced…
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2.720,00 د.إThe Jak 2 Exon 12-15 Mutation Analysis is a specialized genetic test designed to detect mutations in exons 12-15 of the JAK2 gene, which are associated with myeloproliferative neoplasms (MPNs) such as polycythemia vera (PV) and other hematologic disorders. This test offers high sensitivity and specificity, enabling early and accurate diagnosis, which is crucial for targeted treatment decisions and disease monitoring. Unlike standard JAK2 V617F mutation tests, this analysis identifies rare but clinically significant mutations, providing comprehensive genetic profiling for patients with suspected MPNs. Its advanced molecular technology ensures reliable results, supporting personalized therapeutic strategies and improving patient outcomes.
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3.750,00 د.إMitochondrial 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.
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5.500,00 د.إThe Oncomine Acute Myeloid Leukaemia (AML) Panel is a targeted next-generation sequencing (NGS) assay designed for comprehensive genomic profiling of AML. It enables simultaneous detection of key mutations, gene fusions, and copy number variations across clinically relevant genes associated with AML.
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5.375,00 د.إWhole 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.
