In the recent years, more and more companies offer
WES and WGS. Fullgen makes the difference not only
for prices, but also for the quality of the results.
The sum of all coding regions in a genome is called the exome. In humans, this includes 23,000 genes with approximately 50 million bases. With Whole Exome Sequencing (WES), all exons (protein-coding regions) are analyzed. The genetic testing is therefore focused on the analysis of the 1-2% of the human genome where 85% of known pathogenic mutations are found.
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WHOLE EXOME SEQUENCING
In the recent years, more and more companies offer
WES and WGS. Fullgen makes the difference not only
for prices, but also for the quality of the results.
Whole Genome Sequencing (WGS) provides the most comprehensive map of an organism’s genetic make-up. Unlike targeted or exome sequencing, WGS covers all corners of an organisms’ entire genome, which is arguably the most important molecular data.
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WHOLE GENOME SEQUENCING
In the recent years, more and more companies offer
WES and WGS. Fullgen makes the difference not only
for prices, but also for the quality of the results.
This service applies if you already have your sequence made by another company, and you want our team to recheck in bibliography the mutations found. Our deep search will assure a quality result and that no article related to your mutation is overlooked. If we do not find anything new from the report made by the other company, then we will not charge you.
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BIBLIOGRAPHY SEARCH
In the recent years, more and more companies offer
WES and WGS. Fullgen makes the difference not only
for prices, but also for the quality of the results.
Because the costs in sequencing are decreasing every day, what we know today of diseases and their relationships with mutations will surely be increased next year, and next, …. That is why for a minimum annual cost, Fullgen offers the service of deep search every year, to verify if new information related to your illness or mutations was discovered.
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FUTURE SEARCH

WELCOME

COMPANY FULLGEN

Fullgen is a leading global provider of genetic diagnostics and mutation-related disease analyses. We are an interdisciplinary group of doctors, physician, computer scientists and biotechnologists.

We offer the sequencing of your genome individually, confidential and fast. This allows you to detect predisposition to serious illness of genetic origin, both of you and your children.

In addition, Fullgen analyzes a series of related genetic markers with cholesterol, obesity / diabetes and cardiovascular risk, allowing detection genetic trends that can be corrected with adequate health habits.

A pharmacogenetic study is also performed.

Our Services

Whole Exome Sequencing

The sum of all coding regions in a genome is called the exome. In humans, this includes 23,000 genes with…

Whole Genome Sequencing

Whole Genome Sequencing (WGS) provides the most comprehensive map of an organism’s genetic make-up…

Only Bibliography Search

This service applies if you already have your sequence made by another company, and you want our team to recheck in…

Future Searches Fullgen

Because the costs in sequencing are decreasing every day, what we know today of diseases and their relationships with…

COMPANY FULLGEN

Our Services

Whole Exome Sequencing

Whole Genome Sequencing

Only Bibliography Search

Future Searches Fullgen

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