Your full-service lab for clinical trials. Our mission is to ensure the generation of accurate and precise findings.
Basic Care
Basic Health Check
$90
+Complete Blood Count
+Liver Function Blood Test
Heart Disease Blood Tests
Cholesterol / Lipid Levels
Sexually Transmitted Diseases
Male / Female General Health Panel
Comprehensive Metabolic Panel
Essential Care
Gold Health Check
$190
+Complete Blood Count
+Liver Function Blood Test
+Heart Disease Blood Tests
+Cholesterol / Lipid Levels
+Sexually Transmitted Diseases
Male / Female General Health Panel
Comprehensive Metabolic Panel
Total Care
Platinum Health Check
$290
+Complete Blood Count
+Liver Function Blood Test
+Heart Disease Blood Tests
+Cholesterol / Lipid Levels
+Sexually Transmitted Diseases
+Male / Female General Health Panel
+Comprehensive Metabolic Panel
Under construction
Whole Genome Sequencing (WGS) detects sequence and copy changes in DNA through sequencing the protein coding and non-coding regions of the genome to detect genetic variants. WGS is requested when WES fails to show relevant disease-causing variants. When the genome sequence is analyzed, it is compared with the reference human genome. If your WGS reveals potentially disruptive variations relevant to your medical condition, they will be included in your WGS report and shared with your physician who requested WGS. We perform WGS in accordance with the local and international guidelines and standards.
Whole Exome Sequencing (WES)
detects sequence changes in DNA through sequencing the informative regions (protein-coding) of the genome to detect genetic variants. When the exome sequence is analyzed, it is compared with the reference human genome. If your WES reveals potentially disruptive variations relevant to your medical condition, they will be included in your WES report and shared with your physician who requested WES. We perform WES in accordance with the local and international guidelines and standards.
A targeted gene panel
offers a higher depth and coverage for the detection of high and low allele frequencies variants in a group of genes known to be associated with the disease of interest. Gene panels can target groups of diseases like hereditary cancer syndromes, cardiomyopathies, and metabolic diseases. Finding the variants in the disease-relevant genes supports a cost-effective and faster diagnosis, informs treatment and management choices, and continuous monitoring or surveillance for better outcomes and disease prevention.
Cytogenetic Assays To provide genetic diagnosis for many indications such as the blood malignancies, infertility, lethal and debilitating chromosomal defects during and after pregnancy. The chromosomal disorders can result from missing or adding extra chromosomes (or part of chromosome) or complete set of chromosomes, or as a result of structural rearrangements.
What is COVID-19 PCR Test? It is a test that is used to directly screen for the presence of viral RNA of COVID-19 virus. COVID-19 PCR test will detect the viral RNA in the body before antibodies are formed or even symptoms of the disease are present. This means that this test can show if someone has the virus in very early cases.
How the COVID19 PCR test is performed? A nasopharyngeal sample will be collected from the patient and sent to NoorDX Laboratory for PCR test. Substances known as reverse transcriptase or DNA polymerase are added to the nasopharyngeal sample in the laboratory. These substances work to make numerous copies of any viral RNA that may be present. Thus, enough copies of the RNA are present to signal a positive result, as specifically designed primers and probes attach themselves to sequences of the genetic code of the virus to signal that a pathogen has been found.
In NoorDX Laboratory we provide the following COVID-19 test types: -Routine COVID-19 PCR test for travelers. (24 hours) -Urgent COVID-19 PCR test for travelers. (5 hours) -Routine COVID-19 PCR test for contact tracing. (24 Hours)
