Clinical genomic sequencing is a powerful test that can help identify the cause of health and developmental problems. In many cases, clinical exome sequencing or whole genome sequencing (WGS) is used to seek answers for patients where other testing has failed to find a cause of their health problems.
Our clinical genomic sequencing service uses the patient’s clinical presentation (phenotype) as the basis for finding disease causing genetic variants (a phenotype driven approach). We use a multidisciplinary team to provide comprehensive investigation and interpretation, to help support health professionals and patients in finding answers to complex health conditions.
VCGS offers NATA accredited clinical exome and whole genome sequencing.
Genomic sequencing aims to identify any changes or ‘variants’ in the DNA that may cause genetic conditions. The number of variants in a person’s exome is large (thousands). However, most variants do not cause health problems. The challenge for health professionals is to know which variants affect health and which do not. This is why we use a multidisciplinary team of geneticists, scientists and genetic counsellors to determine the significance of any variants found during exome sequencing.
Exome refers to specific parts of DNA that code for proteins. The exome is about 1-2% of our genome – which is the entire set or our DNA.
Genome refers to both the coding and non-coding parts of the DNA. In addition to sequence variant detection, analysis of genome data at VCGS includes the detection of deletions or duplications, also known as copy number variants (CNV).
Clinical genomic sequencing is used to investigate complex health and developmental problems with a suspected genetic cause. 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).
Genomic sequencing technology is also being used to identify many genetic conditions including rare syndromes, cardiac, neurological, and mitochondrial disorders.
Genetic changes identified by genomic sequencing may fall into one of four categories. Testing might identify:
- No genetic variants of significance
- Benign variants that are unlikely to cause genetic conditions
- Pathogenic variants that are known to cause specific genetic conditions
- Variants of unknown significance, which lack evidence to support their nature as benign or pathogenic. Further family testing is often required to determine the clinical significance of these findings.
For either exome or WGS test options, please provide:
- Test request form-> nominate test option (e.g. small, medium, comprehensive, exome or genome)
- Signed informed consent form
- Payment authorisation (for non-Medicare)
- Clinical summary and phenotype details (see pre-approval form and tip sheet below which will help guide collection of appropriate patient information)
- Select targeted gene panels for PanelApp Australia
For paediatricians wanting to order the bulk billed exome for childhood syndromes, please contact us for specific test ordering requirements.
Please contact our team for more information about genomic testing.
P: 1300 118 247
E: [email protected]
Exactly how does exome sequencing work?
To understand sequencing, it’s helpful to understand some basic biology.
The cell is the basic building block of all living things. Humans have billions of cells that contain the genetic information for how the body develops, grows and functions.
This genetic information is stored in DNA. The DNA is ‘housed’ in structures called the chromosomes. DNA is made of four chemicals or bases, represented by the letters A, T, C and G (adenine, thymine, cytosine and guanine). These bases form a unique sequence and changes (or variants) to this sequence can cause disease. A person's entire genetic sequence is known as their genome.
Certain parts of the genome are called genes. Humans have around 23,000 genes and they all play a different role in the body (such as determining eye colour or how we break down certain drugs). It can be useful to think of the genome as a book, where each of the chapters represents a chromosome. Sentences in these chapters would be the genes and the letters that make up each word can be considered the DNA bases. In the case of humans, the book has over 3.2 billion letters.
Exome sequencing is a process that ‘reads’ the particular part of genes that are thought to be most important for health. These parts are called exons. These ‘reads’ contain large amounts of genetic sequence information, which would require hundreds of hours for a scientist to analyse manually. Computers are used to quickly identify variants in the genetic information.
This list of variants is then ‘interpreted’ by comparing the results with databases that list variants known or suspected of being associated with genetic conditions. Interpretation is the most complicated and time-consuming component of exome sequencing because it involves input from many health professionals from different specialties to determine the significance of each variant detected.
What do my results mean?
Once your sample has been tested, a team of experts review any DNA changes or variants found. The team will determine the significance of any variants, using all the available published scientific literature.
Variants fall into a number of categories:
Class 5: Pathogenic Variant:
Pathogenic variants are considered disease-causing
Class 4: Likely pathogenic variant:
The level of evidence that likely pathogenic variants are disease-causing is very high.
Class 3A: Variant(s) of unknown significance with high clinical significance:
VUS with high clinical significance are variants that have evidence to suggest they are pathogenic but there is not enough information to classify them as class 4.
Class 3B: Variant(s) of unknown significance:
Class 3B VUS are variants for which there is insufficient evidence to classify the variant as either disease causing or likely benign.
Class 3C: Variant(s) of unknown significance with low clinical significance:
Class 3C VUS are variant(s) for which the evidence suggests they are likely to be benign.
|No variant of significance was found.||
In some cases, patients might receive an ‘incidental finding’. An incidental or secondary finding is one that is not related to your condition and may have been found by chance. To minimise incidental findings, the laboratory specifically excludes sequencing certain genes known to cause adult-onset cancer, cardiac and neurological conditions. Your doctor will discuss any incidental findings with you and refer if necessary.
What happens to my genetic information?
Genomic sequencing generates a large amount of genetic information. Access to and storage of genetic information is strictly governed by national laboratory and health privacy guidelines. You will be required to sign a consent form for exome sequencing which will describe how your information can be used.