myGenome

myGenome is a genetic sequencing test that is performed from a simple saliva sample. We sequence the entire genome (Whole Genome Sequencing) and issue a complete report of the results. All our tests must be prescribed by a doctor, and include pre and post test genetic counseling.

The entire process from receiving your sample, analyzing the information, and producing your results takes between 12 and 14 weeks. The estimated delivery time varies because every person’s genomic information is unique and may require different degrees of analysis.

myGenome is a test that is designed for healthy people of legal age. For a genetic analysis in minors you have myNewborn, a genetic screening test focused on the most frequent genetic pathologies that appear during childhood.

There are tests that analyze specific positions of your DNA, but they do not study complete genes or the entire genome, these tests are usually cheaper and are known as genotyping tests. If we compare them with a book it would be something like this:

In both cases, the data is real! But the information obtained is totally different. In the first case, if we know what to look at exactly, we will probably get interesting information, although we will leave a lot of information unanalyzed, so the clinical utility is very limited. This may not be visible to the naked eye in the report, but your entire genes are not being analyzed.

On other occasions, the tests sequence the entire genome but do not have teams of professionals in the interpretation of variants, so they include in the report everything that appears in public databases without review and therefore without a final classification. Many of these variants have no clinical utility, so the doctor cannot adapt the medical management and cause unnecessary alarm in the healthy patient.

myGenome is a genetic test that provides clinically important information. For this reason, the test requires a prescription. If you cannot obtain the prescription from your doctor Veritas can provide a genetic counseling consultation (included with the test) and a geneticist will evaluate your case and provide the prescription.

Whole genome sequencing is reading the billions of letters in your DNA, a long chain made up of As, Ts, Cs, and Gs. All your genes are encoded with this 4-letter code, so we analyze your sequence and subsequently look for changes or variants in the genes.

NGS comes from the English term, Next Generation Sequencing, and is used to refer to the set of technologies used to sequence millions of DNA fragments in parallel, improving response times and the cost of genetic tests. Before the implementation of NGS sequencing, sequencing a genome cost millions of dollars.

DNA is the genetic blueprint of life. It is a complex molecule that is found within every cell of our body and contains all the necessary instructions to create and maintain life. It is an information storage system, a code written with four letters that represent four molecules: adenine, thymine, guanine and cytosine. The complete sequence of these chemicals makes up our genetic code, our genome. A single DNA molecule contains around 6 billion A’s, T’s, C’s and G’s, in fact, if you could unfold a DNA molecule it would measure almost 2 meters.

Whole genome sequencing allows all your genetic material to be read by creating a library about you. In this way you will be able to know the relevant information today to prevent and have access to updates in the future, accessing your library again. This trip makes it possible that from now on you can personalize, with the help of your specialist, your health care based on what makes you unique: your DNA.

All people have thousands of genetic variants in their DNA, but it doesn’t mean that they will develop a genetic disease. There are variants that simply make us unique, others that slightly increase our probability of developing a disease, and others that require medical attention because they pose a risk to our health. Interpretation of genetic reports should always be done during a consultation with a genetic counselor to help you understand the information.

Each person can present alterations and variations in their DNA that give them characteristics that make them unique. Detecting these variations is a benefit since it will help to establish guidelines and opportune measures to reduce the possibility of developing the disease and / or treat it in an anticipated and more effective way.

Each person can present alterations and variations in their DNA that give them characteristics that make them unique. Detecting these variations is a bNo, being a carrier of a genetic disease is common. Humans have two copies of each gene. Being a carrier means that you have a genetic variant in one of the copies of a gene associated with a recessive disease. In other words, it has one copy of the gene that works and one copy that does not work. Recessive diseases require that an individual have two variants (the two copies of the gene that do not work) to develop the disease, therefore, you are a “carrier” of a variant, but are not at risk of developing this disease. However, knowing this information is very important since you are at risk of having children affected by this disease if your reproductive partner is also a carrier of the same pathology.

No. The genetic information of a person does not change, what advances is scientific knowledge for which fortunately we know more every day. For this reason, the genome is a resource for life and that can be consulted over time to find out new findings that have been produced thanks to the advancement of scientific knowledge.

The cost of a genetic testing service is related to the technology utilized and the amount genetic expertise is required to provide the result. There is a direct correlation between the amount of DNA information analyzed and the more clinically impactful and reliable the result will be. At Veritas we use whole genome sequencing that allows for the capture and analyzing of all of a person’s DNA. Because the information is so valuable and can significantly impact a person’s future healthcare, we believe it should be managed by a medical professional. We support either directly or in collaboration with the prescribing physician the pre and post-test genetic counseling process where the results are explained and an action plan is established to fully benefit from the information provided.

DNA is not dispersed in our cells, it is carefully packed into structures called chromosomes. We have 46 chromosomes in total, half inherited from our mother and half from our father. Located on these chromosomes are segments of DNA called genes, many of them contain instructions for making proteins, and it is these proteins that determine everything about us, from the color of our eyes to our susceptibility to disease.