🧬 Molecular & Genetic Tests
الفحوصات الجزيئية والوراثية
PCR, DNA sequencing, genetic screening, and molecular diagnostic tests
250 tests in this category
Adenovirus (Respiraitory) PCR
The Adenovirus (Respiratory) PCR test detects genetic material from adenoviruses in a respiratory sample. This test is crucial for identifying an active adenovirus infection, which can cause a range of respiratory illnesses from common colds to pneumonia.
Adenovirus (Stool) PCR
This test detects the genetic material (DNA) of adenovirus in a stool sample. It's a highly sensitive method used to identify an active adenovirus infection, particularly in the gastrointestinal tract, helping pinpoint the cause of digestive symptoms.
AFB RAPID GENOTYPIC TEST (MDR-TB) (Note: This test is not applicable for MOTT)
This rapid genotypic test identifies the presence of Acid-Fast Bacilli (AFB) and checks for specific genetic mutations associated with multi-drug resistant tuberculosis (MDR-TB). It helps in quickly determining if the TB bacteria are resistant to common first-line medications. Please note, this test is specifically designed for Mycobacterium tuberculosis and is not applicable for other types of mycobacteria (MOTT).
AFB SECOND LINE DRUG- GENOTYPIC ASSAY (Note: This test is not applicable for MOTT)
This genotypic assay is used to detect resistance of Acid-Fast Bacilli (AFB) to second-line anti-tuberculosis drugs. It provides critical information when initial treatments are ineffective or if multi-drug resistance is suspected. This test is specifically for Mycobacterium tuberculosis and not for other mycobacteria (MOTT).
AFB-Xpert panel by Genexpert M.Tb detection & Rifamipicin resistance Extra pulmonary samples
This test uses advanced technology to quickly detect Mycobacterium tuberculosis (M.Tb), the bacteria causing tuberculosis, in samples taken from outside the lungs. It also checks if the bacteria are resistant to Rifampicin, a key TB medication.
AFB-Xpert panel by Genexpert M.Tb detection & Rifamipicin resistance pulmonary samples
This advanced test helps detect Mycobacterium tuberculosis (M.Tb), the bacteria causing pulmonary tuberculosis, and checks for resistance to Rifampicin, a key TB drug, using a blood sample. It provides rapid and accurate results.
ALK Fusion - FISH
The ALK Fusion - FISH test is a specialized genetic test that looks for specific changes (fusions) in the ALK gene within tissue samples. These fusions can indicate certain types of cancer, particularly lung cancer.
Amniotic Fluid For Karyotyping
This test analyzes the chromosomes in a sample of amniotic fluid, which surrounds the baby in the womb. It's performed during pregnancy to detect chromosomal abnormalities.
ANTI DNase B; ANTIDEOXYRIBONUCLEASE B
This test measures antibodies produced by your body in response to a recent infection with Group A Streptococcus bacteria. It helps determine if you've had a recent strep infection, even if symptoms have passed.
ANTI DS DNA
This test detects antibodies that target double-stranded DNA, a component of your own cells. It is a key marker used to help diagnose and monitor Systemic Lupus Erythematosus (SLE), an autoimmune disease.
Anti ss DNA Antibody (Single Stranded DNA Antibody)
This test identifies antibodies that target single-stranded DNA in your blood. These antibodies are often associated with certain autoimmune conditions where the immune system mistakenly attacks healthy tissues.
APOE genotyping
APOE genotyping is a blood test that identifies specific variations in the APOE gene. This gene provides instructions for making a protein involved in fat metabolism and brain function. Understanding your APOE genotype can offer insights into certain health risks.
Atopobium vaginae PCR
The Atopobium vaginae PCR test detects the presence of genetic material (DNA) from the bacterium Atopobium vaginae in a urine sample. This bacterium is commonly associated with bacterial vaginosis (BV), a common vaginal infection. The PCR method offers high sensitivity for accurate detection.
BACTERIAL MENINGITIS MULTIPLEX PCR
This test uses an advanced molecular technique (PCR) to rapidly detect the genetic material of multiple bacteria that commonly cause bacterial meningitis. It helps identify the specific type of bacteria responsible for the infection, which is crucial for targeted treatment.
Bacterial vaginosis–associated bacteria 2 (BVAB2) PCR
This PCR test specifically looks for the presence of BVAB2, a type of bacteria strongly associated with bacterial vaginosis (BV). It helps in identifying this specific bacterial marker in a urine sample, offering a non-invasive way to aid diagnosis.
Bacteroides fragilis PCR
This PCR test identifies the genetic material of Bacteroides fragilis, a type of anaerobic bacteria. While often part of the normal gut flora, its presence in other body sites, like urine, can indicate an infection that requires medical attention.
BCR-ABL FISH
The BCR-ABL FISH test uses a special technique called Fluorescence In Situ Hybridization (FISH) to detect a specific genetic change known as the BCR-ABL fusion gene. This gene is a hallmark of certain types of leukemia.
BCR-ABL Kinase Domain (KD) Mutations IRMA
The BCR-ABL Kinase Domain (KD) Mutations IRMA test identifies specific genetic changes within the kinase domain of the BCR-ABL gene. These mutations can impact how effectively targeted therapies for leukemia work.
BCR-ABL qualitative Real Time PCR
The BCR-ABL qualitative Real Time PCR test detects the *presence* or *absence* of the BCR-ABL fusion gene in your blood sample. It's a highly sensitive method to confirm if this specific genetic abnormality is present.
BCR-ABL Quantitative Real-time PCR
The BCR-ABL Quantitative Real-time PCR test measures the *amount* or *level* of the BCR-ABL fusion gene present in your blood. It provides a numerical value, indicating the burden of the gene.
Beta Thalassemia Gene Mutation Analysis
This test analyzes your genes to identify specific mutations linked to Beta Thalassemia. Beta Thalassemia is a genetic blood disorder that reduces the production of hemoglobin, the protein in red blood cells that carries oxygen.
BK Polioma virus Quantitative (Blood)
This test detects and measures the amount of BK polyomavirus DNA in your blood. BK virus is common and usually harmless, but it can reactivate and cause problems in individuals with weakened immune systems, such as organ transplant recipients. Monitoring viral load helps manage potential complications.
BK virus Quantitative (Urine)
This test measures the amount of BK virus DNA present in your urine. While the BK virus is common, its presence and quantity in urine can indicate viral reactivation, especially in individuals with compromised immune systems. It often serves as an early indicator before the virus appears in the blood.
Blood IDH 1/2 PCR
The Blood IDH 1/2 PCR test looks for specific genetic mutations in the IDH1 and IDH2 genes. These mutations are often found in certain types of cancer, particularly brain tumors like gliomas, and can influence how the disease behaves.
Bocavirus PCR
The Bocavirus PCR test detects the genetic material of the Human Bocavirus (HBoV) in a sample, usually from the respiratory tract. This virus is a common cause of respiratory infections, especially in young children.
Bordetella pertussis PCR
This PCR test detects the genetic material of Bordetella pertussis, the bacteria responsible for whooping cough, from a swab sample. It's a highly sensitive test used to identify an active infection.
BRAF - Mutation PCR
This PCR test analyzes a tissue sample to detect specific mutations in the BRAF gene. These mutations can play a role in the development and progression of certain cancers, such as melanoma and some thyroid cancers.
BRCA 1 and 2 MUTATION DETECTION (Germline) with MLPA
This test analyzes your blood sample to detect inherited changes (mutations) in the BRCA1 and BRCA2 genes using MLPA technology. These genes play a crucial role in repairing damaged DNA and preventing tumor growth.
BRCA1 and BRCA 2 mutation detection panel- germline
This blood test screens for inherited mutations in the BRCA1 and BRCA2 genes, which are linked to an increased risk of certain cancers. It helps identify genetic predispositions passed down through families.
BRCA1 and BRCA 2 mutation detection panel- Somatic
This test analyzes a tissue sample, typically from a tumor, to identify acquired (somatic) mutations in the BRCA1 and BRCA2 genes. These mutations develop during a person's lifetime and are not inherited.
C-Kit Mutation PCR Blood
This test looks for specific changes, called mutations, in the C-Kit gene using a blood sample. The C-Kit gene provides instructions for making a protein involved in cell growth and development.
CALR Mutation Analysis
The CALR Mutation Analysis is a blood test that looks for specific changes (mutations) in the CALR gene. These mutations are often associated with certain blood disorders, helping doctors understand the cause of your condition. It provides crucial information for diagnosis and treatment planning.
Campylobacter spp. PCR
The Campylobacter spp. PCR test is a rapid and highly sensitive stool test used to detect the genetic material of Campylobacter bacteria. These bacteria are a common cause of food poisoning and can lead to symptoms like diarrhea, abdominal pain, and fever. This test helps identify the specific pathogen causing your gastrointestinal illness.
Cancer 50 Gene Hotspot Panel NGS
The Cancer 50 Gene Hotspot Panel NGS is an advanced tissue test that analyzes 50 specific regions (hotspots) in genes commonly associated with various cancers. Using Next-Generation Sequencing (NGS) technology, it identifies critical genetic mutations that can drive cancer growth. This test provides a comprehensive genetic profile of your tumor.
Cancer Any Four Gene Panel, NGS
The Cancer Any Four Gene Panel, NGS, is a specialized tissue test that analyzes specific mutations in up to four genes relevant to your particular cancer type. Utilizing Next-Generation Sequencing (NGS), it provides targeted genetic information to help understand your tumor's characteristics. This focused approach aids in personalized treatment decisions.
Candida Albicans Detection, PCR
This urine test uses PCR (Polymerase Chain Reaction) technology to directly detect the genetic material of Candida Albicans. It's a highly sensitive method for identifying the presence of this common yeast, even in small amounts.
Candida dubliniensis PCR
This test uses PCR technology to detect the DNA of *Candida dubliniensis* in a urine sample. It's a highly sensitive method to identify the presence of this specific yeast, which can cause various infections, particularly in individuals with compromised immune systems.
Candida glabrata PCR
This test uses PCR technology to detect the DNA of *Candida glabrata* in a urine sample. It's a highly sensitive method to identify the presence of this specific yeast, which is known to cause various infections, particularly in healthcare settings.
Candida krusei PCR
This test uses PCR technology to detect the DNA of *Candida krusei* in a urine sample. It's a highly sensitive method to identify the presence of this specific yeast, which can cause various infections, especially in patients with weakened immune systems.
Candida lusitaniae PCR
This test uses PCR technology to detect the DNA of *Candida lusitaniae* in a urine sample. It's a highly sensitive method to identify the presence of this specific yeast, which can cause various infections, particularly in immunocompromised patients.
Candida parapsilosis PCR
This test uses PCR technology to detect the DNA of *Candida parapsilosis* in a urine sample. It's a highly sensitive method to identify the presence of this specific yeast, which is commonly associated with infections in healthcare settings.
Candida tropicalis PCR
This test uses a PCR (Polymerase Chain Reaction) method to detect the DNA of *Candida tropicalis*, a specific type of yeast. It helps identify the presence of this fungus, which can cause various infections in the body, particularly in urine samples.
Candidosis, Real time PCR
This Real-time PCR test is designed to rapidly detect the presence of *Candida* species, the yeast responsible for candidosis (thrush or yeast infection). It identifies the fungal DNA, offering a quick and precise diagnosis of the infection from a urine sample.
Chlamydia Trachomatis DNA PCR
This urine test directly detects the genetic material (DNA) of Chlamydia trachomatis. It's a highly sensitive and accurate method to confirm an active infection, even before symptoms appear.
Chlamydophila pneumoniae PCR
This PCR test detects the genetic material (DNA) of Chlamydophila pneumoniae, a bacterium that commonly causes respiratory infections. It's a highly sensitive method to identify an active infection directly from a swab sample.
Chorionic Villi Cells For Karyotyping
Chorionic Villi Cells For Karyotyping is a diagnostic laboratory test available for booking in the UAE. This test helps healthcare providers assess specific health markers and make informed medical decisions.
Chromosomal Microarray 750K
The Chromosomal Microarray 750K is a high-resolution genetic test that scans your entire genome for very small missing or extra pieces of chromosomes (DNA). It's much more detailed than standard chromosome analysis.
Chromosome Analysis (Karyotyping) Peripheral blood
Chromosome Analysis, also known as Karyotyping, is a test that examines the number and structure of your chromosomes, which are the structures holding your genes. It helps identify large-scale chromosomal abnormalities.
Chromosome Interphase Profiling POC
Chromosome Interphase Profiling POC is a rapid genetic test performed on tissue samples, often after a pregnancy loss. It quickly identifies common chromosomal abnormalities in the cells.
cKIT Mutation Screening (Exons 9, 11, 13, 17) Gastrointestinal Stromal Tumors
This specialized test examines specific regions (exons 9, 11, 13, 17) of the cKIT gene within a tissue sample, typically from a tumor. It helps identify mutations commonly found in Gastrointestinal Stromal Tumors (GIST).
CLL Panel FISH
The CLL Panel FISH test uses a special technique called Fluorescence In Situ Hybridization (FISH) on a blood sample. It looks for specific chromosomal changes often associated with Chronic Lymphocytic Leukemia (CLL).
Clostridium difficile toxin A and B PCR
This PCR test detects the genetic material (DNA) of Clostridium difficile bacteria that carry the genes for producing toxins A and B in your stool. It's a highly sensitive method to identify the presence of toxin-producing C. difficile.
Coronavirus 229E PCR
The Coronavirus 229E PCR test detects the genetic material of human coronavirus 229E, a common cause of the common cold and mild respiratory infections. This test helps identify the specific virus responsible for your symptoms.
Coronavirus NL63 PCR
The Coronavirus NL63 PCR test identifies the genetic material of human coronavirus NL63, another common respiratory virus known to cause mild to moderate upper and lower respiratory tract infections, especially in children.
Coronavirus OC43 PCR
This PCR test detects the genetic material of Coronavirus OC43, one of the common cold viruses. It helps identify if your respiratory symptoms are caused by this specific type of coronavirus.
Cryptosporidium spp PCR
This PCR (Polymerase Chain Reaction) test detects the genetic material (DNA) of Cryptosporidium parasites in a stool sample. It's a highly sensitive and rapid method for diagnosing cryptosporidiosis, an infection causing watery diarrhea.
Cyclospora cayetanensis PCR
The Cyclospora cayetanensis PCR test is a highly sensitive molecular test that directly detects the genetic material (DNA) of the Cyclospora cayetanensis parasite in a stool sample. It is used to accurately diagnose cyclosporiasis, an intestinal infection.
CYP 2C 19 Genotyping
This test analyzes your genes to see how your body processes certain medications, specifically focusing on the CYP2C19 enzyme. This enzyme plays a key role in breaking down many common drugs.
Cystic Fibrosis (CFTR) Full gene sequencing
This comprehensive genetic test analyzes the entire CFTR gene to identify specific mutations that cause Cystic Fibrosis. It provides a detailed look at your genetic makeup related to this condition.
Cystic Fibrosis mutation screening (CFTR-Del 508)
This genetic test specifically screens for the Delta F508 mutation, which is the most common genetic change responsible for Cystic Fibrosis. It helps determine if you carry this particular mutation.
DNA Ancestry
This test analyzes your DNA to trace your ancestral origins, revealing insights into your ethnic background and geographical heritage. It helps you discover where your ancestors came from and understand your unique genetic story.
DNA Fitlife
The DNA Fitlife test examines specific genetic markers to provide personalized insights into your fitness potential, nutritional needs, and overall well-being. It helps you tailor your diet and exercise routines based on your unique genetic makeup.
DNA methylation 5 genes pathway
This test analyzes the methylation patterns of 5 specific genes, which are crucial for various bodily functions including nutrient processing and detoxification. Methylation is a vital process that can influence gene expression without altering the DNA sequence itself.
DNA methylation Extended pathway
The DNA Methylation Extended Pathway test offers a comprehensive analysis of methylation patterns across a broader range of genes and pathways. This detailed assessment provides deeper insights into how your genes are being expressed and influenced by environmental factors.
DUCHENNE/BECKER MUSCULAR DYSTROPHY (DMD/BMD) GENE MUTATION
This genetic blood test identifies specific mutations in the DMD gene, which are responsible for Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD). These are progressive muscle-wasting disorders that primarily affect males. The test helps confirm a diagnosis or identify carriers.
EGFR Real time PCR Assay
This test uses Real-time PCR technology to detect specific mutations in the EGFR gene from a tissue sample. It's a precise method for identifying genetic changes that are important for guiding treatment decisions in certain types of cancer.
Entamoeba histolytica PCR
This test uses PCR technology to detect the genetic material of Entamoeba histolytica, a parasite that causes amoebiasis. It's crucial for accurately identifying the presence of this specific pathogen in your system.
Enteroaggregative E. coli (EAEC) PCR
This PCR test specifically identifies Enteroaggregative E. coli (EAEC), a type of bacteria known to cause persistent diarrhea. It helps determine if this specific strain is responsible for your gastrointestinal symptoms.
Enteropathogenic E. coli (EPEC) PCR
This PCR test detects Enteropathogenic E. coli (EPEC), a bacterial strain commonly associated with acute watery diarrhea. It's vital for identifying the specific cause of gastrointestinal infections, particularly in infants.
Enterotoxigenic E. coli (ETEC) PCR
This PCR test identifies Enterotoxigenic E. coli (ETEC), a common bacterial cause of watery diarrhea, often known as "traveler's diarrhea." It helps pinpoint the specific pathogen responsible for your symptoms.
Enterovirus PCR
This PCR test detects the genetic material of enteroviruses, a group of common viruses that can cause a wide range of illnesses. It's used to confirm an enteroviral infection, which can affect various body systems.
Epstein-Barr Virus (EBV), Quantitative PCR
This test detects and measures the amount of Epstein-Barr Virus (EBV) DNA in your blood. It's a quantitative test, meaning it tells you how much of the virus is present, which is useful for monitoring active infections.
Factor V Leiden Mutation (G1691A), QUALITATIVE
This test checks for a specific genetic mutation called Factor V Leiden. This mutation makes one of your clotting proteins (Factor V) resistant to a natural anticoagulant, leading to an increased tendency for blood to clot.
FISH-BMT Sex Mismatch XY Probe
This specialized test uses Fluorescence In Situ Hybridization (FISH) to monitor the success of bone marrow transplantation (BMT) when the donor and recipient are of different sexes. It specifically looks for X and Y chromosomes in the recipient's blood to determine the proportion of donor cells.
FLT3 Gene Mutation Analysis
This test analyzes your blood sample to detect specific mutations in the FLT3 gene. These mutations are commonly found in certain types of leukemia and can influence how the disease progresses and responds to treatment.
FOCUS FUSION 52 GENES PANEL
This advanced genetic test analyzes 52 specific genes in a tissue sample to detect gene fusions. Gene fusions occur when two genes break and rejoin, creating a new, abnormal gene that can drive cancer growth.
Fragile X (FMR1) Mutation Screen
The Fragile X (FMR1) Mutation Screen is a genetic blood test that looks for changes in the FMR1 gene. This test is crucial for identifying the genetic cause of Fragile X syndrome, which is a common inherited cause of intellectual disability.
Gardnerella vaginalis PCR
This PCR test detects the presence of Gardnerella vaginalis bacteria, a common cause of bacterial vaginosis (BV). It's a highly sensitive method to identify the specific genetic material of the bacteria in a urine sample.
GASTRO INTESTINAL PANEL (GI PANEL) PCR
This comprehensive PCR test analyzes a stool sample to detect multiple pathogens, including bacteria, viruses, and parasites, that can cause gastrointestinal infections. It provides a broad overview of potential causes for digestive issues.
Gastrointestinal Bacteria Panel
This stool test specifically identifies various bacterial pathogens that can cause gastrointestinal infections and symptoms like diarrhea, nausea, or abdominal cramps. It uses advanced methods to detect bacterial DNA.
Gastrointestinal Parasite Panel
This stool test specifically looks for parasitic organisms that can infect the gastrointestinal tract, causing symptoms such as chronic diarrhea, weight loss, or abdominal discomfort. It identifies the genetic material of common parasites.
Gastrointestinal Virus Panel
The Gastrointestinal Virus Panel is a test that identifies common viruses responsible for stomach flu and other digestive infections. It helps determine the specific viral cause of symptoms like diarrhea, vomiting, and abdominal pain.
Germline HRR Panel with BRCA 1 and 2
The Germline HRR Panel with BRCA 1 and 2 is a genetic test that looks for inherited changes in genes involved in DNA repair, including BRCA1 and BRCA2. These changes can significantly increase the risk of developing certain cancers.
GI MAP
The GI MAP (Gastrointestinal Microbial Assay Plus) is a comprehensive stool test that analyzes the DNA of bacteria, parasites, and fungi in your gut. It provides a detailed snapshot of your gut microbiome health and function.
GI Map Plus Zonulin
The GI Map Plus Zonulin is an advanced stool test that combines a comprehensive gut microbiome analysis with a measurement of Zonulin. Zonulin is a key biomarker for intestinal permeability, often referred to as 'leaky gut'.
GI360, Stool
The GI360 Stool test is a comprehensive analysis of your gut health, examining various markers in your stool sample. It helps provide a detailed picture of your digestive function, gut microbiome balance, and potential imbalances or infections.
Giardia lamblia PCR
The Giardia lamblia PCR test detects the genetic material (DNA) of the Giardia lamblia parasite in a stool sample. This highly sensitive test is effective in confirming the presence of the parasite, even when only small amounts are present.
Group B streptococcus PCR
The Group B Streptococcus (GBS) PCR test detects the genetic material of GBS bacteria in a urine sample. This test is highly sensitive and provides a rapid and accurate way to identify the presence of GBS, which can be important for pregnant women and newborns.
Haemophilus ducreyi PCR
This is a highly sensitive molecular test that detects the genetic material (DNA) of Haemophilus ducreyi, the bacterium responsible for chancroid. It helps in quickly and accurately identifying the infection.
Haemophilus influenzae PCR
This test uses Polymerase Chain Reaction (PCR) technology to detect the genetic material of Haemophilus influenzae bacteria. It's a highly sensitive method to identify the presence of this specific bacterium in a sample.
Hemochromatosis Common Mutation Analysis in HFE Gene (H63D, S61C & C282Y)
This blood test looks for the three most common genetic changes (mutations: H63D, S61C, C282Y) in the HFE gene. These mutations are strongly associated with hereditary hemochromatosis, a condition where the body absorbs too much iron.
Hemochromatosis HFE Full Gene Sequence Analysis
This comprehensive blood test examines the entire HFE gene sequence to identify any genetic variations or mutations. It's used when common mutation tests are negative but hemochromatosis is still suspected, or for a more detailed genetic assessment.
HEPATITIS B (HBV DNA) VIRUS PCR QUALITATIVE
This highly sensitive test directly detects the genetic material (DNA) of the Hepatitis B virus in your blood. It determines if the virus is present, indicating an active infection.
Hepatitis B Virus DNA PCR (Quantitative) Viral Load
This advanced test measures the amount of Hepatitis B virus (HBV) DNA in your blood. It provides a quantitative viral load, indicating how much virus is present and actively replicating.
HEPATITIS C GENOTYPING
This test identifies the specific genetic type (genotype) of the Hepatitis C virus (HCV) present in your blood. Knowing the genotype is crucial for guiding treatment decisions.
Hepatitis C Virus (HCV RNA) PCR Qualitaive
This test directly detects the genetic material (RNA) of the Hepatitis C virus in your blood. A positive result confirms an active Hepatitis C infection, indicating the virus is currently present and replicating.
Hepatitis C Virus RNA PCR (Quantitative) Viral Load
This test measures the amount of Hepatitis C Virus (HCV) genetic material (RNA) in your blood. It helps determine if you have an active HCV infection and how much virus is present in your system.
Hepatitis Delta virus (HDV) RNA detection by PCR
This highly sensitive test directly detects the genetic material (RNA) of the Hepatitis Delta Virus (HDV) in your blood. It confirms an active HDV infection and is essential for monitoring the viral load, especially in individuals co-infected with Hepatitis B.
HER-2/NEU - FISH
This test uses Fluorescence In Situ Hybridization (FISH) to analyze tissue samples for amplification of the HER-2/NEU gene. HER-2/NEU is a gene that can play a role in the development and growth of certain cancers.
Herpes simplex virus type 1 (HSV 1) PCR
This PCR test specifically detects the genetic material (DNA) of Herpes Simplex Virus Type 1 (HSV-1) in a urine sample. It's used to identify an active HSV-1 infection, often associated with oral herpes (cold sores).
Herpes Simplex Virus Type 1 & Type 2 (HSV 1 & 2) Qualitative PCR
This PCR test directly looks for the genetic material (DNA) of both HSV-1 and HSV-2 in your blood. It's a highly sensitive method to confirm the presence of the virus itself, rather than just antibodies.
Herpes simplex virus type 2 (HSV 2) PCR
This PCR test specifically identifies the genetic material (DNA) of Herpes Simplex Virus Type 2 (HSV-2) in a urine sample. It's a direct and sensitive way to confirm an active HSV-2 infection, commonly associated with genital herpes.
HIV 1 RNA (QUANTITATIVE) VIRAL LOAD
This test measures the amount of HIV-1 genetic material (RNA) in your blood. It provides a quantitative count of the virus, indicating how actively the virus is replicating in your body.
HIV PCR Qualitative
This test directly detects the genetic material (DNA or RNA) of the HIV virus in your blood. It determines if the virus is present or absent, providing a qualitative "yes" or "no" answer regarding infection.
HIV Western Blot Test
The Western Blot test is a confirmatory test used to verify positive or indeterminate results from initial HIV screening tests. It detects specific antibodies to various HIV proteins, providing a highly accurate diagnosis.
HIV/HBV/HCV PCR Qualitative
This test detects the genetic material (DNA/RNA) of HIV, Hepatitis B (HBV), and Hepatitis C (HCV) viruses in your blood. It's a highly sensitive method to identify active viral infections early.
HLA B27 QUALITATIVE PCR
This test identifies the presence or absence of the HLA-B27 gene in your blood. HLA-B27 is a specific protein found on the surface of white blood cells, and its presence is associated with certain autoimmune diseases.
HLA B51
This test detects the presence of the HLA-B51 gene, a specific genetic marker. It helps identify individuals who carry this particular human leukocyte antigen.
HLA-B*57:01 Genotyping (for Abacavir Hypersensitivity)
This genetic test identifies the presence of the HLA-B*57:01 allele in your DNA. This specific gene variant is strongly linked to a severe hypersensitivity reaction to the HIV medication Abacavir.
Human Astrovirus PCR
This test uses PCR (Polymerase Chain Reaction) technology to directly detect the genetic material of Human Astrovirus in a stool sample. Astrovirus is a common cause of gastroenteritis, an infection that leads to diarrhea and vomiting.
Human Norovirus (GI/GII) PCR
This test detects the genetic material of Human Norovirus types GI and GII in a stool sample. Norovirus is a common cause of gastroenteritis, leading to symptoms like vomiting and diarrhea.
Human Papilloma Virus (HPV) Genotyping
This test identifies specific types (genotypes) of Human Papilloma Virus (HPV) from a swab sample. HPV is a very common virus, and certain types can cause health problems like warts or cancer.
Human Rotavirus PCR
This test detects the genetic material of Human Rotavirus in a stool sample. Rotavirus is a leading cause of severe diarrheal disease in infants and young children worldwide.
Human Sapovirus (GI/GII/GIV/GV) PCR
This test identifies the genetic material of Human Sapovirus types GI, GII, GIV, and GV in a stool sample. Sapovirus is another common cause of acute gastroenteritis, similar to Norovirus.
HUNTINGTON DISEASE MUTATION DETECTION
This genetic test looks for a specific mutation in the HTT gene that causes Huntington's disease. It can confirm a diagnosis in individuals with symptoms or identify if someone carries the gene mutation.
IGVH Mutation Detection
The IGVH Mutation Detection test analyzes specific genes in your blood cells, particularly those related to immunoglobulin heavy chain variable regions. This test helps understand the genetic characteristics of certain blood cancers, such as chronic lymphocytic leukemia (CLL).
Influenza A and B virus PCR
This highly sensitive PCR test identifies the genetic material of Influenza A and B viruses. It provides a definitive diagnosis, even in the early stages of infection, making it more accurate than rapid tests.
Influenza H1N1 PCR
This specific PCR test detects the genetic material of the Influenza A H1N1 subtype. It's used to confirm infection with this particular strain, which can cause varying degrees of illness.
Influenza H3N2 PCR
This PCR test specifically targets the genetic material of the Influenza A H3N2 subtype. It helps confirm infection with this strain, which is often associated with more severe illness in older adults and young children.
Jak 2 Exon 12-15 Mutation Analysis
This blood test looks for specific genetic changes (mutations) in exons 12-15 of the JAK2 gene. These mutations are associated with certain blood disorders.
Jak2 exon mutation analysis(V617F) Real Time PCR
This blood test specifically identifies the JAK2 V617F mutation using Real-Time PCR technology. This mutation is a common genetic marker for certain blood cancers.
JC (John Cunningham ) Virus Polioma Quantitative, Blood
This blood test measures the amount of JC virus DNA in your blood. It helps monitor the viral load, especially in individuals with weakened immune systems.
JC (John Cunningham ) Virus Polioma Quantitative, CSF
This test measures the amount of JC (John Cunningham) virus DNA in your cerebrospinal fluid (CSF). It helps assess the viral load, which is important for monitoring active infection in the central nervous system.
JC (John Cunningham ) Virus Polioma Quantitative, Urine
This test measures the amount of JC (John Cunningham) virus DNA in your urine. It helps detect the presence and quantity of the virus shed through the urinary system.
JC/Bk Virus DNA detection CSF
This test detects the presence of DNA from both JC (John Cunningham) and BK viruses in your cerebrospinal fluid (CSF). It's used to identify if either of these polyomaviruses is active in the central nervous system.
JC/Bk Virus DNA detection Plasma
This test identifies the presence of DNA from JC (John Cunningham) and BK viruses in your blood plasma. It helps determine if these viruses are actively replicating and circulating in your bloodstream.
JC/Bk Virus DNA detection Urine
This test detects the presence of DNA from JC (John Cunningham) and BK viruses in your urine. It indicates if these viruses are being shed through your urinary system.
Karyotyping - Products Of Conception
This test analyzes chromosomes from a blood sample to identify any structural or numerical abnormalities. While the test name refers to "Products Of Conception," this blood test is typically performed on parents to investigate potential genetic factors contributing to recurrent miscarriages or stillbirths.
KRAS mutation analysis
This test analyzes a tissue sample to detect specific mutations in the KRAS gene. KRAS mutations are common in certain cancers and can influence how a tumor responds to targeted therapies.
KRAS NRAS HRAS (PAN RAS) Panel NGS
This advanced genetic test uses Next-Generation Sequencing (NGS) to analyze the KRAS, NRAS, and HRAS genes in a tissue sample. It identifies specific mutations within these genes, which are often involved in the growth and spread of various cancers.
KRAS NRAS HRAS BRAF PANEL NGS
This comprehensive genetic test uses Next-Generation Sequencing (NGS) to analyze the KRAS, NRAS, HRAS, and BRAF genes from a tissue sample. It identifies specific mutations within these genes that are frequently associated with various types of cancer.
Lactobacillus spp. PCR
The Lactobacillus spp. PCR test identifies the presence of DNA from various Lactobacillus species in a urine sample. Lactobacillus are beneficial bacteria that play a crucial role in maintaining a healthy microbial balance in the body.
Legionella pneumophila PCR
This PCR test directly detects the genetic material (DNA) of Legionella pneumophila bacteria from a swab sample. It's a highly sensitive and specific method to confirm the presence of the bacteria causing Legionnaires' disease.
LEPTOSPIRA DNA PCR, BLOOD
This advanced test uses Polymerase Chain Reaction (PCR) technology to detect the genetic material (DNA) of Leptospira bacteria in a blood sample. PCR is highly sensitive and can identify the bacteria even when present in very small amounts, offering a precise diagnosis.
LEPTOSPIRA DNA PCR, URINE
This test detects the genetic material (DNA) of the Leptospira bacteria in your urine. It's used to diagnose an active Leptospirosis infection, especially in the early stages when the bacteria might be present in the urine.
Life Geno-DNA based Comprehensive wellness screening panel
Life Geno-DNA based Comprehensive wellness screening panel is a diagnostic laboratory test available for booking in the UAE. This test helps healthcare providers assess specific health markers and make informed medical decisions.
Liquidseq HRR Gene panel [15 genes]
This advanced blood test analyzes 15 specific genes involved in Homologous Recombination Repair (HRR), a critical DNA repair pathway. It helps understand genetic predispositions or changes that can influence cancer development and treatment responses.
Lymphogranuloma venereum PCR
The Lymphogranuloma venereum (LGV) PCR test detects the genetic material of Chlamydia trachomatis serovars responsible for LGV, a sexually transmitted infection. This highly sensitive test helps confirm the presence of the infection.
Lynch Syndrome/NHPCC Gene Panel
This test looks for specific genetic changes in your DNA that are linked to Lynch Syndrome, an inherited condition. Lynch Syndrome increases your risk of developing certain cancers, especially colorectal and uterine cancers. Understanding your genetic status can help you and your doctor make informed decisions about your health.
Malaria Detection by PCR, EDTA Blood
This highly sensitive test detects the genetic material (DNA) of the malaria parasite in your blood. It is crucial for quickly and accurately diagnosing malaria, even at very low parasite levels, which helps guide timely treatment.
Megasphaera Type 1 PCR
This PCR test identifies the DNA of Megasphaera Type 1 bacteria in a urine sample. It's used to detect the presence of this specific bacterium, which can be associated with certain urogenital conditions.
MET Exon 14 Skipping Mutation Detection
This test identifies a specific genetic change, known as MET Exon 14 skipping mutation, in tumor tissue. This mutation can lead to uncontrolled cell growth and is often found in certain types of cancer, particularly non-small cell lung cancer.
Metapneumovirus PCR
This test detects the genetic material of the human metapneumovirus (hMPV), a common respiratory virus. It helps identify if hMPV is causing your cold, flu-like symptoms, or other respiratory infections.
MGMT - PCR
This test analyzes a specific gene called MGMT (O6-methylguanine-DNA methyltransferase) in a tissue sample, usually from a tumor. It uses PCR technology to determine if the MGMT gene is methylated, which can influence how certain brain tumors respond to chemotherapy.
Microarray 750K + NGS Whole Exome Sequencing
This comprehensive blood test combines microarray analysis for detecting large chromosomal changes with Whole Exome Sequencing (WES) to identify specific gene mutations. It offers a detailed look into your genetic makeup.
Mitochondrial DNA Sequencing
This blood test analyzes the entire genetic material found within your mitochondria, the "powerhouses" of your cells. It looks for specific mutations that can cause mitochondrial disorders.
Mobiluncus spp. PCR
This test detects the presence of Mobiluncus species bacteria in a urine sample using PCR technology. It helps identify specific bacteria that can cause certain infections.
MPL GENE MUTATION ANALYSIS
This blood test analyzes your DNA for specific mutations in the MPL gene. These mutations are often associated with certain blood disorders.
MRSA (Methicillin Resistant Staphylococcus aureus) DNA Detection by PCR
This test uses PCR technology to detect the DNA of Methicillin-Resistant Staphylococcus aureus (MRSA) from a swab sample. MRSA is a type of staph bacteria that is resistant to several common antibiotics.
MSI PCR
Microsatellite Instability (MSI) PCR is a test that checks for changes in specific repetitive DNA sequences called microsatellites. These changes can indicate a defect in the DNA mismatch repair system, which is important for correcting errors during DNA replication.
MTHFR (C677T and 1298C) GENE MUTATION, QUALITATIVE
This test identifies specific genetic variations (mutations) in the MTHFR gene, specifically C677T and A1298C. These mutations can affect how your body processes folate (Vitamin B9), which is vital for many bodily functions, including DNA synthesis and repair.
MTHFR (C677T) Mutation Analysis
This test specifically analyzes the C677T mutation in the MTHFR gene. This particular genetic variation can impact your body's ability to convert folate into its active form, which is crucial for various metabolic processes, including detoxification and neurotransmitter production.
Mycoplasma genitalium PCR
This test detects the DNA of Mycoplasma genitalium, a bacterium that can cause sexually transmitted infections (STIs). It's used to identify an active infection, especially when symptoms like painful urination or unusual discharge are present.
Mycoplasma hominis PCR
This test identifies the DNA of Mycoplasma hominis, a type of bacteria commonly found in the genitourinary tract. It helps determine if this bacterium is causing an infection, particularly when symptoms are present or other causes have been ruled out.
Mycoplasma pneumoniae PCR
This PCR test detects the genetic material (DNA) of Mycoplasma pneumoniae directly from a swab sample. It's a highly sensitive and specific method to confirm an active infection, often used for respiratory symptoms like persistent cough or pneumonia.
Myeloproliferative Neoplasia (MPN) Panel (BCR QLT,JAK2 PANEL(12-15),CALR, MPL)
This panel of tests looks for specific genetic changes in your blood cells. It helps identify certain types of blood cancers where your bone marrow produces too many blood cells.
Neisseria gonorrhoeae PCR
This urine test uses PCR technology to detect the genetic material of Neisseria gonorrhoeae, the bacteria that causes gonorrhea. It's a highly sensitive and accurate method for diagnosing this sexually transmitted infection.
NF1 Gene Deletion and Duplication by MLPA
This genetic test uses MLPA (Multiplex Ligation-dependent Probe Amplification) to detect deletions or duplications within the NF1 gene. Changes in this gene are associated with Neurofibromatosis Type 1, a genetic disorder affecting nerve tissue growth.
NGS CNS/Glioma Molecular Panel
This advanced test uses Next-Generation Sequencing (NGS) to analyze multiple genes associated with central nervous system (CNS) tumors, including gliomas. It identifies specific genetic alterations that can influence tumor behavior and response to treatment.
NGS COUPLE CARRIER SCREENING
This Next-Generation Sequencing (NGS) test screens couples for genetic conditions they might unknowingly carry and could pass on to their children. It helps assess the risk of offspring inheriting certain genetic disorders.
NGS COUPLE CARRIER SCREENING + DMD+SMA
This advanced Next-Generation Sequencing (NGS) test screens couples for a broad range of genetic conditions, including specific screening for Duchenne Muscular Dystrophy (DMD) and Spinal Muscular Atrophy (SMA). It provides a comprehensive risk assessment for genetic disorders that could be passed to offspring.
NPM1 Gene Mutation Qualitative
This test looks for specific changes, called mutations, in the NPM1 gene in your blood. These mutations are often found in certain types of acute myeloid leukemia (AML), a cancer of the blood and bone marrow. It helps doctors understand the specific characteristics of the disease.
NRAS Mutation Analysis
This test examines a tissue sample to identify specific mutations in the NRAS gene. These mutations can play a role in the development and progression of various cancers, including melanoma and colorectal cancer. It helps doctors choose the most effective targeted therapies.
OncoHRD ® (Tissue biopsy) A Next Generation Assistive HRD Test
This tissue biopsy test assesses Homologous Recombination Deficiency (HRD), a genetic signature in cancer cells that indicates a weakness in their DNA repair pathways. Understanding HRD status is crucial for selecting specific targeted therapies.
Oncomine Comprehensive myeloid/Leukemia Panel (DNA + RNA fusions)
This comprehensive blood test analyzes your DNA and RNA for various genetic changes, including fusions, linked to myeloid disorders and leukemia. It helps provide a detailed genetic profile to understand these complex blood conditions.
Oncomine Myeloid DNA Panel
This blood test specifically analyzes your DNA for genetic mutations frequently found in myeloid disorders, which are conditions affecting the production of certain blood cells. It provides insights into the underlying genetic causes of these conditions.
Oncomine Myeloid RNA Panel
This blood test focuses on analyzing your RNA for specific gene fusions and expressions related to myeloid disorders. These RNA changes can indicate the presence of certain blood cancers or conditions affecting blood cell production.
Osteogenesis imperfecta gene panel
The Osteogenesis Imperfecta gene panel is a genetic test that analyzes multiple genes associated with "brittle bone disease." It identifies specific mutations that can cause bones to break easily.
Pandemic H1N1/09 virus PCR
This PCR test detects the genetic material of the Pandemic H1N1/09 influenza virus, which causes respiratory illness. It's used to confirm an active infection, helping differentiate it from other common colds or flu strains.
Parainfluenza virus 1 PCR
This PCR test identifies the genetic material of Parainfluenza virus 1, a common cause of respiratory infections, especially in children. It helps diagnose the specific virus responsible for symptoms like cough, fever, and croup.
Parainfluenza virus 2 PCR
This test detects the genetic material of Parainfluenza virus 2 (PIV-2), a common cause of respiratory infections. It helps identify if PIV-2 is responsible for symptoms like cough, sore throat, or fever.
Parainfluenza virus 3 PCR
This test identifies the presence of Parainfluenza virus 3 (PIV-3) by detecting its genetic material. PIV-3 is a frequent cause of respiratory tract infections, particularly in infants and young children.
Parainfluenza virus 4 PCR
This test uses PCR technology to detect the genetic material of Parainfluenza virus 4 (PIV-4), which can cause mild to moderate respiratory infections. It helps determine if PIV-4 is the cause of your respiratory symptoms.
Parvovirus B19 Qualitative PCR
This test directly detects the genetic material (DNA) of Parvovirus B19 in your blood. It's a highly sensitive method to confirm the presence of the virus and diagnose an active infection.
PIK3CA Mutation Analysis
The PIK3CA Mutation Analysis test looks for specific changes (mutations) in the PIK3CA gene within a tissue sample. This gene plays a crucial role in cell growth and survival. Identifying these mutations can help understand the nature of certain cancers.
Plesiomonas shigelloides PCR
The Plesiomonas shigelloides PCR test detects the genetic material (DNA) of the bacterium Plesiomonas shigelloides in a stool sample. This bacterium is known to cause gastrointestinal infections.
PML/RARA (AML - M3 [APML]) by FISH
This test uses a special technique called FISH to look for a specific genetic change, the PML/RARA fusion gene, in your blood cells. This change is strongly linked to a type of blood cancer called Acute Promyelocytic Leukemia (APML).
PML/RARA Qualitative [bcr 1 & 3]
This blood test checks for the presence of the PML/RARA fusion gene, specifically focusing on common breakpoints (bcr1 and bcr3). It helps determine if you have this specific genetic marker associated with Acute Promyelocytic Leukemia (APML).
PML/RARA Quantitative [Single form]
This blood test measures the exact amount of the PML/RARA fusion gene in your system. It's used to track how well treatment for Acute Promyelocytic Leukemia (APML) is working and to detect any remaining disease.
Rapid Whole Exome Sequencing
Rapid Whole Exome Sequencing is an advanced genetic test similar to standard Whole Exome Sequencing but designed for a much faster turnaround time. It analyzes the protein-coding parts of your genes to quickly identify potential genetic causes of medical conditions.
Respiratory comprehensive
This comprehensive respiratory panel is a swab test designed to identify common respiratory pathogens, including viruses and bacteria, that cause infections. It helps determine the exact cause of your respiratory symptoms.
Respiratory comprehensive (12 Hrs)
This rapid comprehensive respiratory panel is a swab test that quickly identifies common respiratory pathogens, including viruses and bacteria, causing infections. It provides results within 12 hours to help guide urgent medical decisions.
Respiratory comprehensive (24 Hrs)
This comprehensive respiratory panel is a swab test designed to identify common respiratory pathogens, including viruses and bacteria, that cause infections. It provides results within 24 hours, offering a balance between speed and thoroughness.
Respiratory comprehensive extended
The Respiratory Comprehensive Extended panel is an advanced swab test that screens for a broader range of respiratory pathogens, including numerous viruses and bacteria, beyond what standard panels cover. It offers a more in-depth analysis of potential causes for respiratory symptoms.
Respiratory comprehensive extended (12 Hrs)
This advanced test quickly identifies a wide range of respiratory pathogens, including viruses and bacteria, from a single swab sample. It's designed for rapid detection, providing results within 12 hours to help guide timely treatment decisions.
Respiratory comprehensive extended (24 Hrs)
This extensive respiratory panel identifies a broad spectrum of viral and bacterial pathogens responsible for respiratory illnesses. Utilizing a swab sample, it delivers comprehensive results within 24 hours to assist in accurate diagnosis and treatment planning.
Respiratory Panel 1
Respiratory Panel 1 is a targeted test designed to identify common viruses and bacteria that cause respiratory infections, such as influenza and RSV. It uses a simple swab sample to help determine the specific pathogen behind your symptoms.
Respiratory Panel 2
Respiratory Panel 2 offers a focused analysis to detect key viral and bacterial pathogens responsible for respiratory tract infections. This swab-based test helps differentiate between various common causes of cough, sore throat, and fever.
Respiratory Panel 3
Respiratory Panel 3 is designed to identify a specific group of respiratory viruses and bacteria that can cause symptoms ranging from mild to severe. This swab test provides valuable information to help your doctor understand the nature of your respiratory illness.
Respiratory Panel 4
The Respiratory Panel 4 test screens for common respiratory viruses that can cause symptoms like cough, fever, and sore throat. It helps identify the specific pathogen responsible for your respiratory illness, guiding appropriate treatment.
Respiratory syncytial virus A and B PCR
This PCR test specifically identifies and differentiates between Respiratory Syncytial Virus (RSV) types A and B, which are common causes of respiratory infections. It offers a highly sensitive method to detect the genetic material of these viruses.
Respiratory syncytial virus A PCR
The Respiratory Syncytial Virus A (RSV A) PCR test specifically detects the genetic material of RSV type A, a common cause of respiratory infections. This highly sensitive test helps confirm the presence of this particular viral strain.
Respiratory syncytial virus B PCR
The Respiratory Syncytial Virus B (RSV B) PCR test specifically detects the genetic material of RSV type B, a common cause of respiratory infections. This sensitive test helps confirm the presence of this particular viral strain.
Rhinovirus A/B/C PCR
The Rhinovirus A/B/C PCR test detects the genetic material of rhinoviruses, which are the most common cause of the common cold. This test can identify the specific type of rhinovirus causing your respiratory symptoms.
Ricketssia DNA Detection by RT-PCR
This test looks for the genetic material (DNA) of Rickettsia bacteria in your blood. It's a highly sensitive method to detect an active infection early, helping doctors identify the cause of your symptoms quickly.
ROS1 - FISH
The ROS1 - FISH test examines tissue samples to look for specific changes in the ROS1 gene. This test is crucial for understanding certain types of cancer, particularly non-small cell lung cancer.
Salmonella spp. PCR
The Salmonella spp. PCR test is a highly sensitive and rapid method to detect the presence of Salmonella bacteria in a stool sample. It works by identifying the genetic material (DNA) of the bacteria, allowing for quick and accurate diagnosis of salmonellosis, an infection that can cause severe gastrointestinal symptoms.
Sarcoma Mutation Analysis
The Sarcoma Mutation Analysis test examines tissue samples from a sarcoma to identify specific genetic changes or mutations. These mutations can provide crucial information about the exact type of sarcoma, how it might behave, and which targeted therapies could be most effective. It helps personalize treatment plans for patients with this type of cancer.
SARS-CoV2-RT-PCR
This test detects the genetic material of the SARS-CoV-2 virus, which causes COVID-19. It's a highly accurate method to determine if you currently have an active infection, even if you have mild or no symptoms.
SARS-CoV2-RT-PCR 12 HRS
This rapid RT-PCR test identifies the genetic material of the SARS-CoV-2 virus, which causes COVID-19, providing results within 12 hours. It's ideal for quickly confirming an active infection, even if symptoms are mild or absent.
SARS-CoV2-RT-PCR 3-4 HRS
This ultra-rapid RT-PCR test detects the SARS-CoV-2 virus's genetic material, providing results within just 4 hours. It's designed for situations requiring the quickest possible confirmation of an active COVID-19 infection.
SARS-CoV2-RT-PCR 6 HRS
This express RT-PCR test detects the genetic material of the SARS-CoV-2 virus, which causes COVID-19, delivering results within 6 hours. It offers a quick and reliable way to confirm an active infection for various needs.
SCA -12(Spino Cerebellar Ataxia) PCR
This genetic test uses PCR to detect specific mutations associated with Spinocerebellar Ataxia Type 12 (SCA12). SCA12 is a rare, inherited neurological disorder that affects coordination and balance, progressively worsening over time.
SCA-1 (Spino Cerebellar Ataxia) PCR
This test uses a blood sample to look for specific genetic changes linked to Spinocerebellar Ataxia type 1 (SCA1). SCA1 is a progressive neurological disorder that primarily affects coordination and balance. It helps identify if you carry the genetic mutation responsible for this condition.
SCA-2 (Spino Cerebellar Ataxia) PCR
This test uses a blood sample to look for specific genetic changes linked to Spinocerebellar Ataxia type 2 (SCA2). SCA2 is a progressive neurological disorder that primarily affects coordination and balance. It helps identify if you carry the genetic mutation responsible for this condition.
SCA-3 (Spino Cerebellar Ataxia) PCR
This test uses a blood sample to look for specific genetic changes linked to Spinocerebellar Ataxia type 3 (SCA3), also known as Machado-Joseph Disease. SCA3 is a progressive neurological disorder that primarily affects coordination and balance. It helps identify if you carry the genetic mutation responsible for this condition.
SCA-6 (Spino Cerebellar Ataxia) PCR
This test uses a blood sample to look for specific genetic changes linked to Spinocerebellar Ataxia type 6 (SCA6). SCA6 is a progressive neurological disorder that primarily affects coordination and balance. It helps identify if you carry the genetic mutation responsible for this condition.
SCA-7 (Spino Cerebellar Ataxia) PCR
This test uses a blood sample to look for specific genetic changes linked to Spinocerebellar Ataxia type 7 (SCA7). SCA7 is a progressive neurological disorder that primarily affects coordination, balance, and often vision. It helps identify if you carry the genetic mutation responsible for this condition.
Shiga toxin producing E. coli (STEC) PCR
The Shiga toxin producing E. coli (STEC) PCR test detects the genetic material of specific E. coli strains that produce Shiga toxins. These bacteria can cause severe gastrointestinal illness.
Shigella/Enteroinvasive E. coli (EIEC) PCR
The Shigella/Enteroinvasive E. coli (EIEC) PCR test identifies the genetic material of Shigella bacteria and Enteroinvasive E. coli, both common causes of bacterial dysentery. This test offers a rapid and accurate diagnosis.
Sickle Cell Anemia Gene Mutation Analysis
This test examines your DNA to identify specific genetic changes (mutations) in the HBB gene that cause sickle cell anemia. It helps confirm a diagnosis of the disease or determine if you are a carrier, meaning you carry one copy of the gene without showing symptoms.
Single Probe - FISH
The Single Probe FISH (Fluorescence In Situ Hybridization) test is a specialized genetic analysis that uses a fluorescently labeled probe to detect a specific genetic change, such as a missing or extra part of a chromosome, within your cells. It provides a highly targeted view of your genetic material.
Small Intestinal Bacterial Overgrowth (SIBO)
This blood test helps assess markers associated with Small Intestinal Bacterial Overgrowth (SIBO), a condition where there's an excessive amount of bacteria in the small intestine. SIBO can lead to various digestive symptoms and nutrient malabsorption.
Solidseq HRR Gene panel [15 genes]
This advanced genetic test analyzes 15 specific genes involved in Homologous Recombination Repair (HRR) pathways using a tissue sample. It helps identify genetic mutations that can affect how cells repair damaged DNA.
STD 1 Panel PCR
This STD 1 Panel PCR test uses advanced technology to accurately detect common sexually transmitted infections from a urine sample. It's a quick and reliable way to screen for specific pathogens, helping you understand your sexual health status. Early detection is crucial for effective treatment and preventing further transmission.
STD 2 Panel
The STD 2 Panel test offers a focused screening for common sexually transmitted infections using a urine sample. It provides essential insights into your sexual health, enabling timely intervention and treatment if needed. This panel is designed for individuals seeking a reliable check-up.
STD 31 Pathogens PCR
The STD 31 Pathogens PCR test offers the most comprehensive screening available, detecting 31 different sexually transmitted pathogens from a single urine sample. This advanced panel provides an in-depth analysis of your sexual health, identifying a wide range of bacterial, viral, and parasitic infections. It's ideal for a thorough understanding of your status.
STD 40+ Panel PCR
This advanced STD 40+ Panel uses PCR technology to detect over 40 common sexually transmitted infections from a single urine sample. It offers highly sensitive and accurate detection of bacterial, viral, and parasitic STIs, even at early stages.
STD 7 Profile
The STD 7 Profile test screens for 7 common sexually transmitted infections using a convenient urine sample. This targeted panel offers a focused assessment of your sexual health, providing clarity on your status regarding key STIs. It's a reliable option for routine screening and peace of mind.
STD 8 Profile
The STD 8 Profile test provides a comprehensive screening for 8 common sexually transmitted infections from a simple urine sample. This panel is designed to give you a clear understanding of your sexual health status, covering a slightly broader range of key pathogens. It's an excellent choice for routine check-ups.
STD PROFILE 14
This test screens for 14 common sexually transmitted diseases (STDs) using a simple urine sample. It's a comprehensive way to check your sexual health and detect infections early, even if you don't have noticeable symptoms.
STD PROFILE 14 (12 Hrs)
This test screens for 14 common sexually transmitted diseases (STDs) using a simple urine sample, with results available in just 12 hours. It offers a rapid and comprehensive way to check your sexual health and detect infections quickly.
STI 28 Profile
The STI 28 Profile is a highly comprehensive urine test designed to detect 28 different sexually transmitted infections. This extensive screening offers a detailed overview of your sexual health, identifying a broader range of potential infections.
Streptococcus pneumoniae PCR
This test uses PCR technology to detect the genetic material of *Streptococcus pneumoniae*. It helps identify infections caused by this common bacterium, which can affect the respiratory system and other parts of the body.
T- Cell Receptor (TCR-B) Gene Rearrangement
This specialized test examines the genetic makeup of T-cells, a type of white blood cell crucial for your immune system. It looks for specific changes, called rearrangements, in the T-cell receptor beta (TCR-B) gene within a tissue sample. These rearrangements can indicate whether a group of T-cells is clonal, which is important for diagnosing certain conditions.
Targeted mutation Analysis (1 mutation)
This test specifically looks for one known genetic change, or 'mutation,' in your DNA. It helps identify a particular alteration that may be associated with a specific health condition or a response to certain treatments.
Targeted mutation Analysis (2 mutations)
This test screens for two specific genetic changes, or 'mutations,' within your DNA. It's used when multiple known genetic variations are relevant to a particular health concern or treatment plan.
Targeted mutation Analysis (3 mutations)
This test identifies three specific genetic changes, or 'mutations,' in your DNA. It is employed when a broader panel of targeted mutations is needed to understand a genetic condition or guide treatment decisions.
Toxoplasma DNA detection by PCR
The Toxoplasma DNA detection by PCR test directly identifies the genetic material (DNA) of the Toxoplasma gondii parasite in your blood. This method is highly sensitive and specific, indicating the presence of an active infection rather than just past exposure.
TPMT GENOTYPING AND TOXICITY TEST
The TPMT Genotyping and Toxicity Test analyzes your genes to determine how your body processes certain medications, specifically thiopurines. This test helps predict your risk of severe side effects from these drugs, which are used to treat conditions like inflammatory bowel disease and some cancers.
Treponema pallidum PCR
The Treponema pallidum PCR test directly detects the genetic material (DNA) of the bacterium that causes syphilis. This highly sensitive test can identify the infection even in its very early stages or when antibody tests might be inconclusive.
Trichomonas vaginalis PCR
The Trichomonas vaginalis PCR test is a highly accurate method to detect the genetic material (DNA) of the parasite Trichomonas vaginalis, which causes the common sexually transmitted infection trichomoniasis. It's a sensitive test for diagnosing active infections.
TSC1 and TSC2 Gene (Tuberous Sclerosis) by MLPA
This test specifically looks for changes in the TSC1 and TSC2 genes, which are associated with Tuberous Sclerosis Complex (TSC). It uses a technique called MLPA (Multiplex Ligation-dependent Probe Amplification) to detect deletions or duplications in these genes.
Typhoid DNA PCR
The Typhoid DNA PCR test directly detects the genetic material (DNA) of Salmonella Typhi bacteria in your blood. This highly sensitive method can identify the bacteria even in the early stages of infection.
Ureaplasma parvum PCR
The Ureaplasma parvum PCR test detects the genetic material (DNA) of Ureaplasma parvum, a type of bacteria, in a urine sample. This highly sensitive test helps identify active infections.
Ureaplasma urealyticum PCR
This PCR test rapidly detects the genetic material of Ureaplasma urealyticum in a urine sample. It's a highly sensitive method for identifying this specific bacterium, which can cause genitourinary infections.
VARICELLA ZOSTER VIRUS (VZV) QUALITATIVE PCR
This test detects the genetic material (DNA) of the Varicella Zoster Virus (VZV) in your blood. It's used to confirm an active infection with the virus responsible for chickenpox and shingles.
Vibrio cholera PCR
This PCR test specifically identifies the genetic material of *Vibrio cholerae*, the bacterium responsible for cholera. It's used to quickly and accurately diagnose cholera infection from a stool sample.
Vibrio parahaemolyticus PCR
This PCR test detects the DNA of *Vibrio parahaemolyticus*, a bacterium commonly associated with seafood-related food poisoning. It helps identify the cause of gastrointestinal illness, particularly after consuming raw or undercooked seafood.
Vibrio vulnificus PCR
This PCR test identifies the genetic material of *Vibrio vulnificus*, a bacterium that can cause severe infections, especially in individuals with underlying health conditions. It's used to diagnose infections from contaminated seafood or exposure to contaminated water.
Whole Exome Sequencing
Whole Exome Sequencing (WES) is a powerful genetic test that examines all the protein-coding regions of your genes, known as the exome. It helps identify genetic variations that may be linked to inherited diseases or health conditions.
Whole Exome Sequencing (TRIO)
Whole Exome Sequencing (TRIO) is a comprehensive genetic test that examines all the protein-coding regions of your genes (exome). The "TRIO" aspect means the test is performed on the patient and both biological parents, which helps identify inherited genetic changes more effectively.
Whole Genome Sequencing (30x)
Whole Genome Sequencing (WGS) is the most comprehensive genetic test, analyzing nearly all of your DNA, including both coding and non-coding regions. It provides a complete map of your genetic makeup.
Wilson disease (ATP7B) gene analysis
This genetic test analyzes the ATP7B gene to identify mutations associated with Wilson disease. Wilson disease is a rare inherited disorder that causes copper to accumulate in vital organs, leading to serious health issues.
X and Y Identification- FISH
This test uses Fluorescence In Situ Hybridization (FISH) to accurately identify the presence and number of X and Y chromosomes in your cells. It's vital for diagnosing conditions related to sex chromosome abnormalities.
Y Chromosome Microdeletion (16 Mutations)
This genetic test specifically looks for small deletions (microdeletions) on the Y chromosome, focusing on 16 known mutations. These deletions are a significant genetic cause of male infertility.
Yersinia enterocolitica PCR
This test detects the genetic material of Yersinia enterocolitica bacteria in a stool sample. It helps diagnose infections caused by this bacterium, which can lead to gastrointestinal issues like diarrhea and abdominal pain.
Zika Virus Detection by Real TIme PCR, Blood
This test uses Real-Time PCR technology to directly detect the genetic material of the Zika virus in a blood sample. It's used to confirm an active, ongoing Zika infection, especially in the early stages.
Zika Virus Detection by Real TIme PCR, Urine
This test uses Real-Time PCR to detect the genetic material of the Zika virus in a urine sample. It's often effective for diagnosing active infections, as the virus can be detectable in urine for a longer period than in blood.
Zonulin, Stool
This test measures zonulin levels directly in a stool sample. Stool zonulin provides a localized assessment of intestinal permeability, reflecting the integrity of the gut lining where zonulin is produced and released.