Oncology Tests

Are you the father? Why not get the answers you need today with a home paternity test? Our paternity test is accurate, confidential and easy to carry out. Your results will be ready in just 5-7 working days. Our test uses comprehensive genetic markers to ensure 99.99% accuracy and assurance.

Do you share one biological parent, or both biological parents? Or perhaps none? EasyDNA offers sibling DNA testing services to help siblings discover whether individuals tested are full siblings, half siblings or no siblings at all.

Celiac disease genetic testing can accurately confirm whether you have a genetic predisposition to celiac disease. Around 83% of celiac diseases suffers go undiagnosed. Could you be one of them? Celiac disease is a serious genetic autoimmune disorder and could lead to long-term complications that could adversely affect your life.

Grandparentage DNA testing can be used when grandparents need to confirm the biological relationship to their grandchild. This test will show the statistical probability that the grandparents are genetically related to their grandchild.

At EasyDNA we offer DNA testing for Immigration purposes. Our DNA tests are ISO 17025 accredited and can be presented alongside immigration documents as proof of relationship, helping to support other immigration documentation.

Cheating is no longer about guess work. Our infidelity DNA test is ideal to help provide a good indication of whether or not cheating has taken place. Clients can send in a variety of different samples which have roused their suspicions. An infidelity test can be carried out using a range of DNA samples including nail clippings and hairs. Once the DNA samples are at our laboratory, you will receive your comprehensive DNA analysis report in 10 working days.

Experience discomfort when eating dairy products? Do you feel bloated or get indigestion after consuming foods such as milk or cheese? If the answer to these questions is Yes, then you may need a lactose intolerance test. A lactose intolerance test will establish whether you carry certain a gene mutation which makes you unable to produce the enzyme which helps digest lactose.

The aunt-uncle DNA test (or avuncular test) will determine whether a genetic relationship exists between aunts and/or uncles and their niece and/or nephew. Avuncular test results will show you a probability of relationship between tested parties.

Was your child born through surrogacy? Do you need to claim Australia citizenship by descent for your child? We at easyDNA Australia can help you by proving you with the most accurate and reliable surrogacy DNA testing services. A DNA test result will provide incontrovertible proof of relationship between the commissioning parents/s and the child born through surrogacy treatment outside Australia. easyDNA offers NATA accredited paternity and maternity DNA surrogacy testing services.

Unlocking the secrets behind what makes you unique starts with a simple saliva DNA sample! Do you like to play it safe or are you more of a risk taker? Are you a Planner or are you more Spontaneous? Learn about how your genetics affects your behaviours from stress management to Sociability. Karmagenes knows you better than you know yourself!

A Y chromosome test (Y-STR test) is used to determine if males tested share the same paternal lineage. The test is highly accurate and results are provided in just 7 working days from the receipt of samples at our laboratory.

Genetic Testing Laboratories offer a full range of forensic testing services. Below are the most common samples we test and the list includes the success rate, price as well as packaging information for each sample. Please note these prices are an add-on to the test you order. “Not Available in conjunction with Express Testing.”

Expecting? Will it be a boy or a girl? Find out with our baby gender test. EasyDNA offers an avant-garde and highly scientific baby gender prediction DNA test that can be done at 8 weeks post conception or 10 weeks of pregnancy. Our test is performed in an accredited laboratory using a blood sample and offers an accuracy of 98%.

Are you ready to take the next step towards a healthier, fitter you? Nutrifit utilises cutting edge Next Generation Sequencing Technology coupled with leading bioinformatics and modern scientific research. This extensive test comprises 35 different analyses and instead of just analysing a couple, NutriFit assesses over 110 genetic variations, setting us apart from many other tests on the Market

Think your partner might be cheating? Have you found a stain which you suspect might be semen? Use our semen detection test.

We are pleased to announce a very Special Prenatal Package which includes our Non Invasive Prenatal Paternity Test, Non Invasive Prenatal Screening Test for Down’s Syndrome and many other Chromosomal Disorders.

Have you ever wanted to discover your very own geogenetic links, your true ancestral heritage? You might have an idea of your recent ancestors but you can only discover your ancient, deep ancestral origins with an ancestry DNA test. Results ready in 3 weeks from receipt of samples.

A genetic reconstruction test is designed to establish if a child is biologically related to direct blood relatives on their father’s side of the family. The test is performed when the father in question cannot be directly involved in the test and a direct father-child paternity test cannot be carried out.

EasyDNA offers an accurate twins DNA test which will establish whether twins are identical or fraternal. Our test is 100% accurate and results are ready in 5-7 working days.

Why take any risks with your prenatal paternity test? EasyDNA offers a non invasive prenatal paternity test. Starting at 10 weeks from conception (this means you will be in your 10th week of pregnancy, starting from the first day of your last menstrual period) with 0 risk. Confirm the paternity of your unborn baby with a 99.9% accurate test that requires only blood samples from the mother and alleged father.

EasyDNA offers you the possibility of generating your own unique genetic DNA profile. Every individual has a unique genetic make-up and therefore can be identified through their profile. EasyDNA will analyse 21 genetic markers and provide you with a report that can be used to identify you uniquely. DNA Profiling can therefore be used for a wide variety of purposes.

A DNA maternity test is used to determine a biological relationship between an alleged mother and a child. The test works in the exact same way as the DNA paternity test and the results guarantee minimum probabilities in excess of 99.99%+ for inclusion of maternity, and 100% for exclusion.

EasyDNA can now offer the most comprehensive non-invasive prenatal genetic screening test available – Our ‘Prenatal Peace’ (also called NIFTY™) test is a 100% safe test that screens for Down’s syndrome and 17 other genetic conditions. Starting at just 10 weeks of pregnancy and using only a maternal blood sample, this test can provide more accurate results compared to traditional screening methods. This test also includes Gender Determination upon request for no extra charge.

We offer Genetic Predisposition DNA Test for Health and Disease. It is an innovative test which allows you to discover whether you are genetically predisposed towards developing a number of diseases and medical conditions. With this test we can help you and your family to live longer and healthier life. What are you waiting for? Act now before it’s too late. Invest in your health. Hurry and call us now!

EasyDNA offers clients the option to include an electropherogram with their DNA test results. An electrogpherogram is a graphical representation of the raw data from one’s DNA sequence and is unique to every individual. EasyDNA offers electropherograms with all DNA tests available as an added service.

Our Inherited Cancer Panel specifically looks for inherited gene mutations in over 130 different genes associated with a wide range of hereditary cancers (including BRCA1, BRCA2 & PALB2). This screening test can be used to identify gene mutations responsible for hereditary cancers and to clarify the genetic risk for individuals with a family history of these hereditary cancers. It is a powerful tool that can help you reduce your risks or undertake measures that will help you detect hereditary cancers as early as possible.

TSP19™ is a Targeted Sequencing Panel covering 19 genes involved in myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML).

Lupus is a life-long, autoimmune disorder that causes the body’s immune system to become hyperactive and attack normal body tissues. It can damage the internal organs and affect all body systems in the long run.

Testing of the protein coding region of the genome (exome) covering more than 19,000 genes can be performed from FFPE cancer samples. For inherited diseases a blood sample would be required.

Need to confirm if someone is a drug user? Hair Drug testing is a process in which a hair sample collected from a donor’s head or body is screened for the use of illicit substances. Hair analysis can accurately detect drugs used up to 90 days prior to the test and has been proven to be five times more effective than urine tests! Results are available in 3 to 5 working days. Choose between Anonymous and Legal testing.

As an ongoing commitment to patient care, EasyDNA has added additional comprehensive multigene panels for cancer analysis to its diagnostic next generation sequencing molecular testing range of assays. EasyDNA has associated NATA accredited laboratories in Australia to provide this comprehensive cancer analysis assay covering both DNA mutations and RNA fusion genes.

The quest to identify a relatively non-invasive, patient-friendly, effective cancer biomarker has continued and a solution to previous problems has now been found with the development of new technologies and techniques including sequencing technologies, massive parallel sequencing and highly sensitive quantitative polymerase chain reaction (PCR) testing.

The assay covers 26 genes associated with soft tissue sarcomas: ALK, CAMTA1, CCNB3, CIC, EPC, EWSR1, FKHR, FUS, GLI1, HMGA2, JAZF1, MEAF6, MKL2, NCOA2, NTRK3, PDGFB, PLAG1, ROS1, SS18, STAT6, TAF15, TCF12, TFE3, TFG, USP6 and YWHAE.

Our tumour mutational load assay has been designed in response to the need to determine if treatment utilising immune checkpoint inhibitors are likely to be of benefit in your particular clinical circumstances.

This specialized panel includes analysis of the BRCA1 and BRCA2 genes. BRCA1 and BRCA2 gene mutations can increase your risk of breast and ovarian cancer and are implicated in a high number of breast cancer cases.

Graves’ disease is an autoimmune disorder of the thyroid gland that triggers overproduction of thyroid hormones. It is more common in women and usually begins after age 20. The thyroid gland releases thyroxine (T4) and triiodothyronine (T3), the hormones which control body metabolism. Balanced metabolism is critical for regulating mood, weight, and mental and physical energy levels.

Celiac disease, also referred to as CD in short, is a lifelong autoimmune condition which directly affects the small intestine, a part of the gastrointestinal tract that accounts for 90% of all food absorption. Due to the fact that Celiac disease affects the digestive system, mainly the small intestine.

Multiple sclerosis (or MS) is a chronic, often debilitating disease that strikes the central nervous system (CNS), which is made up of the brain, spinal cord, and optic nerves. It is an inflammatory disease wherein the fatty myelin sheaths covering the axons of the brain and spinal cord are damaged.

Psoriasis arises when the immune system erroneously identifies a normal skin cell as a pathogen, and communicates incorrect signals that lead to overproduction of new skin cells. It is a recurring, chronic, non-contagious condition of the skin characterised by red skin with silvery scales and itchy, dry red patches called plaques that are sometimes painful.

TSP50™ is a Targeted Sequencing Panel covering 50 genes involved in cancer. This panel is ideal for patients diagnosed with ovarian cancer, breast cancer, prostate cancer and bladder cancer, providing analysis of genes that may offer suitable drug targets.

Atrial Fibrillation occurs when the two upper chambers of the heart start beating with an abnormal rhythm. This occurs as a result of an abnormality in the electrical impulses that regulate heartbeat.

Aneurysm is a localized balloon-like protrusion in the wall of a blood vessel. Aneurysms usually develop in arteries at the base of the brain (the circle of Willis) and an aortic aneurysm develops in the main artery that carries blood from the left ventricle of the heart. Venous aneurysms also happen but arterial aneurysms are much more common.

Coronary Heart Disease (CHD), also called coronary artery disease occurs when plaque accumulates in the arteries that supply blood to heart muscle, called coronary arteries.

TSP22™ is a Targeted Sequencing Panel covering 22 genes associated with lung cancer, bowel cancer, melanoma and pancreatic cancer. For lung cancer, we are also able to screen for RNA fusions including ALK, RET, ROS-1 and NTRK-1.

Venous thrombo-embolism (VTE) is a condition whereby blood clots form in the blood, these then travel through the blood veins. If a blood clot forms which is large enough it can block the supply of blood to important organs.

Overview of Macular degeneration: Age related macular degeneration (AMD) is an age-dependent cause of legal blindness (visual acuity of 20/200 or worse) and one of the highly reported cases across the world. Management of AMD is a challenge as it is considered as non-curable; however few clinical cases can be treated with laser-photocoagulation. As the overall life-expectancy of the world increases, so does the prevalence of AMD.

Alzheimer’s disease is an irreversible, progressive brain disease that causes deterioration of cognitive functioning, such as thinking and memory skills, to an extent that it interferes in a person’s ability to function in every day life. Alzheimer’s disease appears most commonly in people over 60 years of age. Alzheimer’s disease is the most common form of dementia found in old age.

Pharmacogenomics (PGx) is the analysis of how genes affect a person’s response to drugs. This relatively new field combines pharmacology (the science of drugs) and genomics (the study of genes and their functions) to develop effective, safe medications and doses that will be tailored to a person’s genetic make-up. PGx is able to provide information about a patient’s genetic likelihood to respond to a given medication or risk of an adverse drug response (ADR).

Obesity is defined as a medical condition in which excess fat has accumulated in the body to the extent that it constitutes a risk to a person’s health. A person is considered to be obese if he or she has a bodyweight that is at least 20% higher than it should be.

Migraines are non specific pains in the head that are often difficult to diagnose. People often confuse migraines and headaches because the two are both essentially pains in the head. A migraine is in fact a headache, but it is a very intense headache; we can thus say that somebody who has a migraine does in fact have a type of headache.

Type 1 Diabetes is known by many other names; the most common ones include juvenile diabetes, insulin dependent diabetes and Diabetes Mellitus Type 1. It is one of the autoimmune diseases in which the beta cells of the pancreas, which create an important hormone (called insulin), are destroyed and consequently the pancreas produce little or no insulin at all. The result is that with not enough insulin in the body, the glucose fails to get absorbed in the cells for energy and the blood sugar level rises.

Type 2 diabetes is the most common form of diabetes, and occurs when the pancreas does not produce enough insulin, or the body is not able to metabolise the insulin properly, a process called insulin resistance. Insulin is the hormone responsible for regulating glucose levels in the blood. This will lead to elevated levels of insulin in the blood. Type 2 diabetes tends to develop slowly, and a person may be unaware that he or she has type 2 diabetes.

Colorectal cancer is general term which refers to cancer of the large intestine, and which includes both colon cancer, which is a cancer which forms in the colon, the longest part of the large intestine, as well as rectal cancer which is cancer of the rectum last several inches of the colon closest to the anus.

Bladder cancer is a malignancy which arises from epithelial lining of the urinary bladder. It is so severe in the sense that these abnormal cells increase in number uncontrollably in the bladder.

Breast cancer occurs when cells in the breast start reproducing abnormally to form a malignant tumour. Breast cancer most often begins in the cells of the lobules, which are the glands that produce milk, or the ducts, the passages through which milk passes from the lobules to the nipple.

Postnatal Peace is proud to be able to offer Nova™.

Nova™ is a newborn screening test that determines a baby’s risk for 50 inherited disorders, as well as providing personalised genetic information on the metabolism of 20 drugs. Nova™ utilises Next Generation sequencing technology, coupled with the leading genetics bioinformatics software. Postnatal peace is able to offer the most comprehensive and accurate newborn screening test that is over 99.99% accurate.

Our Inherited Disease Panel tests for over 300 genes with over 700 unique inherited diseases, including neuromuscular, cardiovascular, developmental, and metabolic diseases and is often used to show a genetic compatibility between a couple or exclude it.

Gastric cancer is a cancer of the stomach. Cancer occurs when cells in a particular area of the body start reproducing abnormally and invade the surrounding body tissue. Stomach cancers tend to develop slowly over many years, and starts off from pre-cancerous changes which often occur in the cells of the lining of the stomach. These early changes rarely cause symptoms and therefore often go undetected.

Lung cancer is results from an uncontrolled division and proliferation of cells that eventually forms a mass known as a tumour in the lungs. Lung cancer is the most common cause of death due to cancer in both men and women throughout the world.

The prostate gland is part of the male reproductive system and its role is to produce an important buffering constituent of semen. A buffer is a chemical that balances out the PH, neutralizing the acidity caused by urine passage in the tracts – this acidity would kill the sperm cells.

EasyDNA offers the latest genetic research related to your child’s physical and behavioural tendencies. Find out how your child’s genes influence who they are and what they can be with this affordable DNA test kit. Get your results in 6 to 8 weeks. Gain valuable, scientific information about everything from cognitive abilities to your kid’s physical attributes.

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EasyDNA offers a highly accurate, non-invasive prenatal paternity test with 0% risk – a scientific breakthrough in the field of prenatal testing. Your other, invasive prenatal paternity testing options are risky – with them you stand a chance of miscarriage or harming the baby. Our non-invasive test is the safest and most accurate test available.

The NATA DNA paternity testing can be used to settle a range of family related legal matters, for example in child custody cases, to change a birth certificate, inheritance disputes and immigration applications. The NATA accredited paternity test starts from $550 for testing alleged father, mother and 1 child.

Autism is a lifelong condition that belongs to a group of neurodevelopmental disabilities known as Autism Spectrum Disorders (ASDs). Our Autism screening Panel analyses over 230 genes associated with ASD and can aid in diagnosis of patients with suspected ASDs. For many children and adults, the everyday life can be significantly improved by a diagnosis and appropriate specialist support.

TSP50™ is a Targeted Sequencing Panel covering 50 genes involved in cancer. This panel is ideal for patients diagnosed with ovarian cancer, breast cancer, prostate cancer and bladder cancer, providing analysis of genes that may offer suitable drug targets.

TSP22™ is a Targeted Sequencing Panel covering 22 genes associated with lung cancer, bowel cancer, melanoma and pancreatic cancer. For lung cancer, we are also able to screen for RNA fusions including ALK, RET, ROS-1 and NTRK-1.

This DNA test will assist you with the help you need to tune your lifestyle with your genes in common areas of your nutrition requirements, sports, natural rejuvenation and health. So Are you ready to take the next step towards a healthier, fitter you? Nutrifit utilises cutting edge Next Generation Sequencing Technology coupled with leading bioinformatics and modern scientific research.

This test can only be purchased as an add on to Nutrifit

Are you ready to take the next step towards a healthier, fitter you? NutriPlan utilises cutting edge Next Generation Sequencing Technology coupled with leading bioinformatics and modern scientific research. This extensive test comprises 35 different analyses and instead of just analysing a couple, NutriPlan assesses over 110 genetic variations, setting us apart from many other tests on the Market

This test can only be purchased as an add on to Nutrifit