About Us
WHY WE’RE DIFFERENT
EXCLUSIVE PARTNERS
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Genomics throughout Life
Genomic testing is useful in many stages in life, right from pregnancy planning through to old age.
Childhood
Some diseases may be due to new (de novo) mutations in a child, that were not present in the parents. Additionally, some parents may not have had the opportunity to have screening testing and may have an affected child even though they themselves may not show symptoms. Genomics testing such as our Newborn Genetic Screening Test, can screen for inherited genetic disorders and may help to confirm a diagnosis.
Cancer
Our cells are constantly replicating and being replaced by new cells generated by our bodies. Cancer is caused by errors in the genome, known as mutations which can occur randomly when copying, by environmental damage or a genetic predisposition. We offer a range of genomic testing options designed specifically for cancer patients that may help identify specific mutations that are unique to each patient’s cancer and help healthcare providers make informed choices on the best treatment options for their patients, in addition to a wide portfolio of genetic testing tailored for commercial targeted therapies provided by oncology pharmaceutical sector.
Inherited Disease Screening
For a range of inherited conditions and disorders, symptoms do not always allow for a definitive diagnosis to be made. Basing a diagnosis on clinical symptoms alone can also result in an incorrect or delayed diagnosis. Obtaining an accurate diagnosis through genetic testing can have significant positive outcomes for patients and their health care providers, by clarifying the diagnosis and helping to identify treatment options sooner. It can also assist in identifying the risk of occurrence in family members, who may be carriers of a genetic mutation. Codex genetics center has one of the largest genetic testing options of any laboratory in Egypt. Our testing range covers over 3,000 genes associated with a whole range of inherited disorders.
What is Targeted Sequencing?
Codex utilizes targeted sequencing panels, where we look at a select number of genes associated with particular conditions. This enables only part of the genome to be looked at helping to keep costs and turnaround times down, to improve patient outcomes.
Reducing the number of genes, we look at means we can look more in depth at certain genes, sequencing a particular region more than a hundred times and in some cases more than ten thousand times, so that we can be confident in the result obtained.