Introducing GSeek Exome
Gseek Exome is the most comprehensive test to find any inherited or acquired mutation. The exome is the only test which looks at all the protein coding areas in the DNA. The proteins are responsible for any changes in the physical make up or internal make up of each individual. The GSeek Exome confirms changes in protein formation that could be causes of various diseases and their subsequent implications. GSeek covers close to 22,000 referenced genes, and pseudogenes.
How to get answers to a non confirmed diagnosis
GSeek Exome identifies any disease based on the exome regions in the DNA. The exome region is the protein-encoding area which is majorly responsible for genotypic and phenotypic information. The information helps identify these referenced protein changes across multiple databases. The precision allows a patient even with new mutations to be diagnosed. Many rare diseases or undiagnosed medical problems would benefit from this test.
Benefits of the GSeek Exome test include:
- Detailed information on the molecular basis of each individual’s protein coding ares(exome)
- Indicates whether the individual has any changes affecting the manufacture of proteins
- Helps physicians to have a confirmed diagnosis especially with a large differential list or rare disease
- Gives a physician and patient a clear way forward in terms of future care and treatment
Whole Exome Sequencing
Genetic testing and genomic data will give an individual an insight into their physical and functional makeup based on their DNA. Healthcare professionals globally can use this data to plan treatment and followup up care.
GSeek Exome
Credence GSeek Exome covers 22,000 genes and their exonic areas. The exonic areas are the protein-encoding areas. The protein-encoding areas represent disease changes seen in an individual;
Key points
- Get the benefit of the most accurate way to identify protein coding mutations
- Most accurate and comprehensive test
- Understand all available prevention and treatement options
- To be done in consultation with your physician and a genetic counsellor
- Benefit from early diagnosis and reduced medical costs
Did you know?
Medical diagnosis and treatment is now drifting away from trial and error based standard medicine (where all patients with similar category of symptoms are prescribed with a single drug – one size fits all approach) to more efficacious, cost effective, personalized treatments with no side effects.