
Genome
Full genome sequencing and interpretation to help you live a longer and healthier life
are due to the inheritance of a genetic variant that predisposes to a tumor.
of having a child affected by a genetic disease.
are due to gentic variations in genes responsible for the structure of the heart's muscle or heart rate.
Aqquired factors like sedentary life or the lack of physical activity rises this risk.
are due to adverse drug reactions.
- We will inform you of your risks from 200+ diseases of genetic origin.
- You will learn about 40+ diseases that could be transmitted to your children.
- We will offer you data on 15 multifactorial diseases, which depend on genetics and environmental factors.
- You will understand how your body will react to 110+ drugs based on your genetics.
- We will provide you with information on +50 genetic traits related to diet, athletics, longevity, nutrition, metabolism and more.
- You will learn about your ancestors.
- A genetic counsellor approved by medmesafe will accompany you before and after the analysis by video consultation.

- 13 weeks from reception of sample in laboratory

- Only available in Spain

- Collection of saliva.

- Genome sequencing with Illumina HiSeq X Ten/Nova Seq with an average coverage of 30X (reference coverage in genome analysis).
- 99% analytical sensitivity for Single Nucleotide Variants and 97.6% for small insertions/deletions (6 bases).
- Analysis and classification of variants with internal and external databases (ClinVar and Human Gene Mutation Database).
- Variant screening carried out by an expert team with its own software developed for the detailed classification of variants.
- For monitoring and quality control each sample is processed in Infinium QC Array-24 microarray (Illumina).
Testimonials
Rod Paley

Graeme McKenzie

Daniel Crigan

Our partner labs, nationally and internationally certified




We put at your disposal more than 150 extraction points, the largest network in Spain.
70–80% of tumors are unrelated to ancestry. Only 5 or 10% of tumors can be explained by a specific genetic alteration that directly causes the onset of the disease. In the remaining 15-20% of cases, there are familial characteristics that contribute to the onset.
Germ mutations occur in the ovule or sperm and are inheritable. In most inherited cancer syndromes, the chance of a child inheriting the family mutation is 50%.
It is important to note that being a carrier of a mutation is not synonymous with cancer, it means having a higher risk of developing one or more types of cancer. "
- 25% of the children will be totally healthy.
- 50% will be healthy carriers.
- 25% will have a genetic disease.

How does it work?
-
Select desired analysis and a specialist, then you have a video-consultation.
-
Receive a sample collector kit at home that will be picked up by a courier.
-
One of our partner labs makes the analysis.
-
Your healthcare professional presents your results via videoconference.
You can help by sharing this information with your contacts or doctor