What can sequencing test be used for?
Clinical sequencing is used to investigate complex health and developmental problems. It’s often used by specialist groups, such as geneticists and neurologists, to investigate specific causes of well-known, but poorly understood conditions (like intellectual disability or brain malformations).
Analysis is phenotype driven and relies in the first instance on targeting genes specific to the phenotype.
We have around 20,000 genes in every cell of our body. Genes are made up of DNA, which contains a four-letter chemical code: A, G, C and T.
Each gene contains thousands of letters. The sequence of these letters is important, just like the letters and words in an instruction manual.
Our entire genetic code (genome) is made up of six million base pairs, tightly packaged into chromosomes. Chromosomes come in pairs, and we inherit one from each parent.
How does it affect me?
Only about 2 per cent of our genetic material is used to form proteins, the building blocks of life. We have increasing knowledge that suggests the rest of our genetic material (the other 98 per cent) can still affect how our genes work. We all have changes (variants) in our genes. Most of the time, these variants are harmless and do not affect our health. For example, variants contribute to eye colour and height.
Sometimes, variants can make a gene faulty and can result in a genetic condition. For example, spelling mistakes in genes or missing parts of chromosomes. These variants are often called a ‘mutation’ or ‘gene fault’.
Variants can be inherited from one or both parents, and they can occur spontaneously (not inherited). Diet, lifestyle, and environment can also contribute to the risk of developing a health condition.
What is genetic testing?
Genetic testing investigates variants in our genes, chromosomes, or proteins. A genetic test might investigate a single gene, search for large changes or rearrangements in our chromosomes or analyse the proteins formed from genes. Genetic testing also encompasses newer forms of investigations called genomic testing.
What is genomic testing?
Genomic testing allows us to investigate vast amounts of the genetic sequence in one go. Until recently, doctors and scientists were only able to test one gene at a time. Genomic testing on the other hand, allows testing of many genes or the entire genome at once. This is particularly useful when there are several genes associated with a condition, or it is unknown which gene may be the cause.
Genomic testing can be used to help diagnose rare genetic conditions and provide information about the chances of relatives and children having the condition. However, there are many other important uses for genomic testing.
There are different types of genomic testing that your healthcare professional might mention, including:
Gene Panels – investigates a defined number of genes, that could include tens to thousands of genes.
Whole Exome Sequencing (WES) – investigates the areas of DNA that are used to form proteins (~2% of the genome).
Whole Genome Sequencing (WGS) – used to investigate our entire genome, including the DNA that is not used to form proteins.
What is required for testing?
You will need a referral form filled out by your GP or healthcare specialist. Once you have confirmed that you wish to proceed with testing, we can provide you with the necessary referral forms to be filled out and signed by your doctor.
We require a blood sample for testing and blood sample collection can be done at your local pathology at an additional cost. The sample collection fee is not included in the test price.
The testing fee includes your sterile kit which will be sent to your address, the testing services, your DNA test report sent to your doctor and your return express courier for your samples.
Results will be available within 2 months after receipt of specimen in our partner laboratory and will be emailed to your GP as soon as they are available.
Contact us to find out more