Reliable DNA testing Center in Dubai

Onelife health care center provides expert and best DNA testing center in Dubai.

One Can easily book a DNA testing in Dubai easily with a simple call.
Just Call: 0509796922
Appointment: Immediate Availability no waiting and get DNA tested done at home comfort.

What is Gene Testing:

Gene tests examine your DNA to identify specific changes (mutations) that can increase your risk of developing or causing genetic conditions. These tests can focus on a single gene, multiple genes, or your entire DNA makeup, which is called genomic testing.

A gene test analyzes your DNA to identify changes (mutations) in your genes. These changes can affect your health in various ways, including increasing your risk of developing certain diseases, influencing your response to medications, and determining your susceptibility to environmental factors.

Types of Gene Tests:

• Diagnostic gene tests: Confirm or rule out a suspected genetic condition.
• Predictive gene tests: Estimate the likelihood of developing a genetic disease in the future.
• Carrier gene tests: Determine if you carry a gene for a genetic condition that you may pass on to your children.
• Pharmacogenetic tests: Identify how your genes may affect your response to medications.
• Prenatal gene tests: Detect genetic abnormalities in a fetus.

Importance of Gene Testing:

• Early detection: Can help identify diseases early when treatment is most effective.
• Personalized medicine: Allows for tailored treatment plans based on individual genetic makeup.
• Family planning: Helps couples understand their risk of passing on genetic conditions to their children.

Chromosome Testing

A chromosome test analyzes the number and structure of chromosomes in a person's cells.

Chromosomes are thread-like structures found in the nucleus of every cell. They contain DNA, the genetic material that determines inherited traits.

Why is it done?

• To detect chromosomal abnormalities: These can lead to genetic disorders like Down syndrome, Turner syndrome, or Klinefelter syndrome.
• To diagnose birth defects: Certain birth defects are associated with chromosomal changes.
• To determine the sex of a fetus: By examining the sex chromosomes (X and Y).
• To investigate infertility issues: Sometimes, chromosomal abnormalities can affect fertility.

DNA test can lead to detect genetic disorders like Down syndrome, Turner syndrome, or Klinefelter syndrome, Huntington's disease,Cystic fibrosis,Sickle cell disease,Phenylketonuria,Colon (colorectal) cancer,Breast cancer.

Some tests identify genetic risk factors for specific health conditions. Consult a healthcare professional for comprehensive health risk understanding.

It Can test all types of genetic testing . Below

ColoComprehensive |IHC, ER-PR & Her2 by IHC |HER2 By FISH |HER2 By Digital PCR |BRCA1&2 by NGS - BRCA1&2 |Somatic BRCA 1&2 |
OncoCEPT - Solid |EGFR by NGS |EGFR T790M |OncoCEPT-Liquid |HPV 16/18 |HPV-high risk strains |OncoCEPT Solid Comprehensive | KRAS+NRAS+BRAF Oncocept Solid - Onco.colon |GIST Panel Oncocept Solid - Onco.GIST | Thyroid Cancer Panel OncoCEPT Solid - Onco.Thyroid |
Oncocept Solid Breast Cancer Panel (ER+Her2-) - Onco.Breast |HRR Gene Panel |Oncocept Solid Single Gene - Onco.single

Microsatellite Instability - Onco.MSI |MMR IHC PANEL for MSI |IHC Marker PDL1 |ORION whole Exome/ Comprehensive Cancer/ Inherited Cancer Germline | Karyotyping from Blood |Karyotyping from Amniotic Fluid |Chromosome 21 for trisomy (Down's Syndorme) | Sex Chromosome-X/Y |Pre/ Postnatal FISH Panel- 13, 18, & 21 | FISH for Pre/ Postnatal Chromosome 13, 18, 21, X and Y | Y-chromosomal microdeletion |

"CytoScan Optima/POC Microarray/Cytoscan 315K/Microarray Rapidsure/Constitutional/ Di George by Microarray/ Prader Willi-Angelmann by Microarray | Prenatal Microarray/ Cytoscan 315K* (MCC is recommended) | Cytoscan 750K/Microarray Rapidsure Deepdive | Non Invasive Prenatal Testing- Focus | Non Invasive Prenatal Testing- Comprehensive | Non Invasive Prenatal Testing- Plus | Beta Thal Trio
Prenatal Sanger Validation | ORION-TRIO-PROBAND | Prenatal ORION | Lumous Plus (Female)/LUMPLUSFEM | Lumous Plus (Male)/LUMPLUSMAL
Lumous Comprehensive (Female)/LUMCOMPFEM | Lumous Comprehensive (Male)/LUMCOMPMAL | Lumous Focus (Female)/LUMFOCSFEM | Lumous Focus (Male)/LUMFOCSMAL | PGS FOR 1 EMBRYO (Extended)/PGT-A | PGT-SR | Pre PGD Work-Up | PGD 1 Embryo/PGT-M | Sperm DNA Fragmentation Study

TORCH PCR | Endometrial Receptivity Assay (ERA) | HLA - A,B,C,DR,DQ High resolution by NGS | HLA Test Package For Cadaver Recipient (HLA Typing, PRA & Single antigen) | HLA - A,B,C,DR,DQ low resolution by Luminex | HLA - A,B,DR low resolution by Luminex
HLA - A |HLA - B |HLA B 1502 |HLA - C |HLA - DR | HLA - DQ High Resolution | HLA DQA1 |HLA (DRB1 and DQA1)

HLA DRB 3,4,5 |HLA -G |DSA By Luminex (HLA Cross Match |LCM-CDC | Lymphocyte Auto donor cross matching |Lymphocyte Auto Patients cross matching | Lymphocyte DTT treated serum cross matching |Single Antigen Class-I |Single Antigen Class-II
Panel Reactive Antibody HLA- Class-I | Panel Reactive Antibody HLA- Class-II |Antibody screening for HLA Class I & II
MIC-A Single Antibodies Panel | Flow cytometery lymphocyte (T and B cell) cross match
MIC-A Typing | KIR Genotype |BCR-ABL1 (IS) by Real-time PCR | BCR-ABL1 Qualitative Multiplex for Detection of Transcript

JAK2 V617F Mutation Study by Real-time PCR (V617F) | JAK2 Mutation Panel (Exons 12 to 15) | Onco haem (DNA+RNA) (AML and B-ALL By NGS)
Onco haem: DNA only by NGS | Onco haem: RNA only by NGS | Chimerism Study Mutation Analysis | PML-RARA Fusion Gene Detection (Qualitative) |PML-RARA Fusion Gene Detection (Quantitative) | Karyotyping From Bonemarrow | Del(5q) by FISH | Del(7q) By FISH
Del(20q) By FISH | E2A/TCF3 detection by FISH | IgH By FISH | INV 16 by FISH | TEL-AML by FISH | AML1-ETO By FISH | MLL By FISH | 11q (ATM) By FISH | 17p (p53) By FISH | PDGFR Alpha By FISH | PDGFR Beta By FISH | PML-RARA Detection By FISH |BCR-ABL1 By FISH

Trisomy 8 by FISH | ALL Panel By FISH |AML Panel By FISH | CLL Panel By FISH |MDS Panel By FISH | MM Panel By FISH |Stress Cytogenetics
MYEOV/IGH by FISH t(11;14) | BCL2/IGH (Follicular lymphoma) By FISH | BCL-6 By FISH |ORION (Whole Exome Sequencing with CNV calling, WES)
ORION Focus (Clinical exome based disease panels) | ORION (Single gene) | ORION Trio (Whole Exome Sequencing) | Mitochondrial Genome sequencing | Prenatal ORION |BRCA1&2 by NGS - BRCA1&2 | Beta thal common mutations | Beta Globin Gene Sequencing | Beta globin Trio / Beta thal trio | Congenital adrenal hyperplasia testing: CYP21A2 analysis (seq+ MLPA)/ Congenital Adrenal Hyperplasia (Seq+MLPA)

Duchenne Muscular Dystrophy (DMD) by MLPA | Fragile X syndrome | Huntington Disease Molecular Assay | Maternal cell contamination
Spinal Muscular Atrophy (SMA) By MLPA | Sanger validation | Aneuploidy detection by QF-PCR | Prenatal microarray (Cytoscan Optima)
Microarray Constitutional | Microarray Rapidsure Deepdive/Microarray 750K | Lumous Plus (Female)/LUMPLUSFEM |Lumous Plus (Male)/LUMPLUSMAL
Lumous Comprehensive (Female)/LUMCOMPFEM | Lumous Comprehensive (Male)/LUMCOMPMAL |Lumous Focus (Female)/LUMFOCSFEM |Lumous Focus (Male)/LUMFOCSMAL

Cost of DNA Genetic testing  Price In Dubai ?

• Our Lab are ECIA accredited CAP accredited you are planning to go for DNA testing the price range from 1500 Aed - 18000 Aed.

Where Can you book a DNA testing In Dubai

• Contact: 0509796922 
• Availability :24x7
• Certification: CAP/ ECIA certified & DHA licensed facility 
• Appointment: Instant Appointment available.

DNA test times vary by test type and provider. Results can be available within a few days to a few weeks. Confirm specific timelines with thechosen provider.