About GENvip

Our research group uses the latest analysis techniques for molecular genomics and cellular biology (“omics”)

Our mission is to advance and promote knowledge on the genetic basis of infections and to contribute to the development of individualized strategies for their prevention and treatment.

Through the combined analysis of genomes, transcriptomes, epigenomes, and integrative biology (cell culture, gene editing), GENVIP investigates the biological basis of infections using a novel host-based approach, and explores solutions for clinical practice through biomarkers.

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our team

GENVIP is formed by a multidisciplinary and cross-functional team in the field of basic and applied clinical research

Led by Profesor. Federico Martinón-Torres (Head of the Department ofPediatrics, University Hospital Complex of Santiago and Professor of Pediatrics at the University of Santiago), a pediatrician with experience in clinical practice and research in the field of infectious diseases, and by Profesor Antonio Salas Ellacuriaga (Faculty of Medicine of the University of Santiago deCompostela) a geneticist of international repute.

We use the latest technologies and analysis techniques from different disciplines to optimize the understanding, diagnosis, prevention and treatment of infections.

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Our research areas

We conduct studies on genomics, transcriptomics, epigenomics and proteomics, as well as bioinformatics analysis focused on infections and vaccines

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Find out what we can do for you

Our service includes all the support required for your project, from experiment advice and consultation to technical support for the development of sequencing protocols, material management, sample analysis and bioinformatics data analysis for publication.

We use our platforms for Direct Digital Molecular Detection (Nanostring's nCounter MAX) and Sequencing (NextSeq2000 from Illumina).

The technology and services offered by GENVIP through this Platform provides significant advantages for medium throughput sequencing options. Some of the most common applications of this system include whole human exome sequencing, mRNA sequencing and gene panels or single gene sequencing. Thanks to the flexible technology, the platform can be adapted to a wide range of applications and used in projects with different sequencing targets.

In addition, we now offer the Single Cell Service The Chromium X series provide access to single cell analysis at any stage.

It offers cost-effective single cell analysis, making it the right technology to perform single cell assays at any scale with the greatest flexibility.

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