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Submitted URL: http://veritasgenetics.com/
Effective URL: https://www.veritasint.com/
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Submission: On May 30 via api from DE — Scanned from DE
Effective URL: https://www.veritasint.com/
Submission Tags: tranco_l324
Submission: On May 30 via api from DE — Scanned from DE
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<p style="font-size: 12px;"><span style="font-family: Helvetica, Arial, sans-serif;">From time to time, Veritas Intercontinental may send you emails with information related to our products and services which we think may be of interest to you.
You can opt out by using the unsubscribe link in such communications, changing your account settings or, if you do not have an account, you can email us at dpo@veritasint.com</span></p>
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HOME
IMPROVING HEALTHCARE THROUGH GENETICS
Our test based on whole exome and genome sequencing provides the interpretation
of extensive genetic information that can be further analyzed in the future.
CLINICALLY
RELEVANT
We use the most advanced technology to transform genetic data into clinically
relevant information with the purpose of providing insights to improve a
person’s quality and length of life.
PHYSICIAN
ASSISTED
All our services require counselling. It is vital that the correct analysis is
recommended and that the findings are managed by a medical professional with
expertise in genetics.
RESOURCE
FOR LIFE
Our genome and exome based genetic tests generate the complete data of an
individual’s DNA that can be reanalysed in the future to provide genomic updates
or targeted studies as science advances.
OUR SERVICES ENCOMPASS THREE AREAS OF GENETICS
All our genetic tests require a genetic consultation to evaluate which of our
services is suitable. Veritas can support this process by providing pre and
post-test genetic counselling to assess what tests are suitable, the
interpretation of results and, if necessary, the design of an action plan for
future healthcare management.
PREVENTIVE MEDICINE
The most comprehensive genetic service, based on whole genome sequencing, for
disease prevention and healthcare.
Genetic test to assess the risk for common diseases.
Polygenic risk screening for common diseases.
PERINATAL MEDICINE
Non-invasive prenatal test that studies the most frequent chromosomal
abnormalities.
Screening for early childhood onset diseases.
The most complete genetic care for your baby that brings together myPrenatal and
myNewborn.
Study of chromosomal abnormalities and spontaneous termination of pregnancy
DIAGNOSTIC GENOMICS
Hereditary cardiovascular disease risk.
Hereditary cancer risk.
Whole genome and exome sequencing for patients with a complex medical history or
symptoms suggesting a genetic origin, in order to find out the possible
underlying cause.
WHY ARE GENETICS IMPORTANT IN PREVENTIVE HEALTHCARE MANAGEMENT?
17%
17% of people have genetic variants that increase the risk of diseases.1
20%
Up to 20% of cancer cases are related to hereditary factors.2
20%
Around 20% of sudden cardiac deaths are due to genetic abnormalities.3
5%
5% of patients are hospitalised for adverse drug reactions.4
86%
86% of people are asymptomatic carriers of a monogenic disease that can be
transmitted to their offspring if the partner is a carrier of the same disease.5
9%
Up to 9,4% of newborns may have genetic variants linked to early onset childhood
diseases.6
Bibliographic references
1Hou YC et al. Precision medicine integrating whole-genome sequencing,
comprehensive metabolomics, and advanced imaging. Proc Natl Acad Sci U S A 2020
Feb 11;117(6):3053-3062.
2https://seom.org/informacion-sobre-el-cancer/consejo-genetico.
3Orland KM et al. Molecular Autopsy for Sudden Cardiac Death: Current State and
Considerations. Curr Genet Med Rep 2019;7:145–152.
https://doi.org/10.1007/s40142-019-00170-x.
4Bouvy JC et al. Epidemiology of Adverse Drug Reactions in Europe: A Review of
Recent Observational Studies. Drug Saf 2015;38:437–453.
5Hou YC et al. Precision medicine integrating whole-genome sequencing,
comprehensive metabolomics, and advanced imaging. Proc Natl Acad Sci U S A 2020
Feb 11;117(6):3053-3062.
6Holm, Ingrid A., et al. “Thee BabySeq project: implementing genomic sequencing
in newborns.”BMC pediatrics 18.1 (2018): 225.
COMMENTS FROM OUR CUSTOMERS
The main reason I chose to have the analysis was to understand my genetics and
how it can potentially affect my children. I believe that it is better to know
and understand my options for prevention.
Laura F., 36
myGenome gave me access to an important preventive healthcare resource, allowing
me to know my genetic risks and act accordingly to improve my quality of life.
Antonio S., 41
I am very interested in genetics and its importance in the future of healthcare.
I chose to have the myGenome analysis because of the scope of information that
it provides from my risk to cancer to interesting traits that have helped me
better understand my body.
Carlos Roberto M., 45
The main reason I chose to have the analysis was to understand my genetics and
how it can potentially affect my children. I believe that it is better to know
and understand my options for prevention.
Laura F., 36
myGenome gave me access to an important preventive healthcare resource, allowing
me to know my genetic risks and act accordingly to improve my quality of life.
Antonio S., 41
I am very interested in genetics and its importance in the future of healthcare.
I chose to have the myGenome analysis because of the scope of information that
it provides from my risk to cancer to interesting traits that have helped me
better understand my body.
Carlos Roberto M., 45
The main reason I chose to have the analysis was to understand my genetics and
how it can potentially affect my children. I believe that it is better to know
and understand my options for prevention.
Laura F., 36
myGenome gave me access to an important preventive healthcare resource, allowing
me to know my genetic risks and act accordingly to improve my quality of life.
Antonio S., 41
I am very interested in genetics and its importance in the future of healthcare.
I chose to have the myGenome analysis because of the scope of information that
it provides from my risk to cancer to interesting traits that have helped me
better understand my body.
Carlos Roberto M., 45
PreviousNext
--------------------------------------------------------------------------------
WHAT IS DNA?
Your DNA is composed of a very long string of molecules. The information encoded
in your DNA is responsible for everything from the colour of your eyes to how
you respond to certain drugs.
THE AGE OF GENOME BEGINS
Whole genome sequencing allows you and your physician to make better choices for
your health and the health of your loved ones.
SEE ALL VIDEOS
FREQUENTLY ASKED QUESTIONS ABOUT OUR GENETIC TESTS
When is genetic testing recommended?
Genetics has an impact on many areas of health and can be clinically useful both
to prevent and diagnose diseases. At Veritas we offer you genetics for life,
genetics aimed at living a healthy life. The first step is to request a
consultation with one of our genetic counsellors.
What are genetic test with clinical utility?
GeneGenetic testing is based on the analysis of a person’s genes, Veritas tests
are clinically useful because we perform an extensive analysis on select genes
with solid scientific evidence. In addition, our geneticists conduct a secondary
review on all variants discovered to ensure that all results are correctly
validated.
Who should consider using the services offered by Veritas Intercontinental?
At Veritas we have a wide range of tests developed for individuals who are
looking for genetic information to take care of themselves in a more proactive
and personalised way. We also provide genetic services for individuals who
present a series of signs, symptoms or medical history in which it is necessary
to carry out a genetic diagnostic test. Depending on each case, our genetic
counsellors will recommend the appropriate analysis.
What is Whole Genome Sequencing (WGS)?
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.
What is the NGS?
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.
What is DNA?
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.
Why sequence the entire genome?
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.
What does it mean to have a genetic variant?
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.
It is bad to be a carrier of a genetic mutation?
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.
Will I suffer for a certain disease because I am a carrier of a disease of
genetic origin?
No, 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.
Can my Genome change over time?
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.
Why does pricing for genetic test vary so much?
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.
What are chromosomes?
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.
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