Laboratory code (LABCODE)

about Us

Laboratory code (Labcode) was established in 2018 as private Sector Company.

The main objective of Labcode is to bring Genetic and Genomic Medicine technology to serve public in both government and private sectors conveninently such as NPS, NIPT, and NGS gene analysis in genetic diseases. To date, genetic and genomic technology has a large barrier in clinical service due to the expensive cost and the institutes that can perform the tests are not widely available. Labcode is well supported all patients and companies to have the best technology, TAT, quality and prices. Therefore, LabCode is a send-out testing service provider that specializes in delivering the world's highest quality testing with a wide testing portfolio in partnership with one of the world's pioneering and largest testing providers.

Pairing decades of experience in newborn screening, with over seven million newborns screened since 1994 and a state-of-the-art clinical genomics program provides one of the world’s most comprehensive programs for detecting, analyzing and reporting clinically significant genomic changes. The laboratory is accredited and registered by CAP, CLIA, JCHO, COLA and CDC.

We are able to provide hospitals and clinicians anywhere in MENA easy access to the most advanced genetic testing at globally competitive pricing and highest quality standards.

Gene analysis of several genetic disorders is more feasible and less expensive than in the past. LabCode also has a consultation service for physicians. LabCode includes medical technologists, who are specialized in genetic and genomic technologies. The staff members are highly motivated in this field and well disciplined, in order to provide the best quality service to the public.

OUR
Value

To make lives better together through health and healing.
We do what is right for each patient
We continually strive to be patient-centered.
We respect the uniqueness and honor the dignity of each patient with our words and unspoken acts.
We communicate openly and honestly with our patients.
We hold patient confidentiality in the highest regard.
We protect the integrity of the patient record.

OUR SERVICES

CLINICAL GENOMICS

 

Whole Genome Sequencing

The genome comprises all of a person’s the DNA. The exome, the protein-coding portion of the genome, only accounts for about 1-2% of the genome. The exome is the part of our DNA that contains protein-coding genes, and accounts for approximately 1-2% of our total amount of DNA (genome). Whole Genome Sequencing is a genetic test that analyzes all of the DNA in a person’s Genome.

Whole Exome Sequencing

The exome is the part of our DNA that contains protein-coding genes, and accounts for approximately 1-2% of our total amount of DNA (genome). Whole Exome Sequencing is a genetic test that analyzes all of the genes (~22,000) that make up an individual’s exome.

Array™

The Array™ genetic test leverages genomic sequencing technologies and bioinformatics tools to detect large copy number changes (CNV) throughout the genome. First-line test for patients with intellectual disability or global developmental delays.

First-line test for individuals with multiple congenital anomalies

Patients with autism/autism spectrum disorders (ASDs).

Patients with suspected chromosomal imbalances including micro-deletion syndromes.

Suspected uniparental isodisomy

Suspected autosomal recessive condition due to close familial relations (consanguinity)

Previously negative karyotyping and/or chromosomal microarray results.
Determine breakpoints of chromosomal rearrangements previously detected by conventional cytogenetic methods, BAC arrays, and other less sensitive arrays

AnyPanel™

The AnyPanel™ test is exactly as it sounds, “any panel.” Whether you are choosing from a list of over 200 expertly-curated panels or creating your own custom panel, we strive to meet the needs of our clients and patients. Since the AnyPanel™ test can be customized based on a patient’s clinical symptoms and subsequent differential diagnosis, this test can be used in most instances where genetic testing is being considered.

BIOCHEMICAL SCREENING & GENETICS

Newborn Screening

The StepOne® Comprehensive Biochemical Profile is one of the most comprehensive biochemical newborn screening tests in the world, with the ability detect more than 50 disorders in newborns from just a few drops of blood. The StepOne® Comprehensive Biochemical Profile is a newborn screening test that can detect more than 50 disorders in newborns from just a few drops of blood.

Biochemical & Metabolic Testing

Our complete biochemical testing menu pairs biochemical assays (such as enzyme analysis) with a multitude of genetic testing options to ensure that providers have both the tools that they need, along with the options that that they prefer, when treating and diagnosing biochemical and metabolic conditions.

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