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

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BIENVENIDO

EMPRESA FULLGEN

Fullgen es un proveedor líder mundial de diagnósticos genéticos y análisis de enfermedades relacionadas con mutaciones. Somos un grupo interdisciplinario de médicos, médicos, informáticos y biotecnólogos.

Ofrecemos la secuenciación de su genoma de forma individual, confidencial y rápida. Esto le permite detectar la predisposición a enfermedades graves de origen genético, tanto de usted como de sus hijos.

Además, Fullgen analiza una serie de marcadores genéticos relacionados con el colesterol, la obesidad / diabetes y el riesgo cardiovascular, lo que permite detectar tendencias genéticas que pueden corregirse con hábitos de salud adecuados.

También se realiza un estudio farmacogenético.

Nuestros Servicios

Secuenciación Completa de Exome

La suma de todas las regiones codificantes en un genoma se denomina exoma. En humanos, esto incluye 23,000 genes con …

Secuenciación del Genoma Completo

La secuenciación completa del genoma (WGS) proporciona el mapa más completo de la estructura genética …

Solo Búsqueda Bibliográfica

Este servicio se aplica si ya tiene su secuencia realizada por otra compañía, y desea que nuestro equipo la vuelva a verificar en …

Búsquedas Futuras Fullgen

Debido a que los costos en la secuenciación están disminuyendo todos los días, lo que sabemos hoy de enfermedades …

EMPRESA FULLGEN

Nuestros Servicios

Secuenciación Completa de Exome

Secuenciación del Genoma Completo

Solo Búsqueda Bibliográfica

Búsquedas Futuras Fullgen

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