As part of the ASCIRES Biomedical Group, we have been working for over 40 years in precision diagnosis using specialisation and bringing together two cutting-edge areas: diagnostic imaging and genetic diagnosis. Because of this duality we can develop personalised integrated solutions.

We are pharmogenetic experts, a specialisation that allows us to identify and prescribe treatments and drugs on an individual basis, according to the patient, their response and development.

We are working to provide a solution for the challenges posed by the pharmaceutical sector and the scientific world. The clinical research they develop is becoming more expensive and more complex, meaning we have to work on multi-centre clinical trials.

AREAS OF SPECIALISATION

SG Oncobytes®

In-depth genetic study and analysis of each cancer cell from a point mutation to the sequencing of the whole exome.

This connects patient data using clinical procedures, bioinformatics analysis of the information, clinical-biological interpretation and setting personalised treatment.

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Clinical Trials

We develop integrated genetic solutions for the process of launching next-generation treatments.

We contribute to the development of multi-centre clinical trials for clinical research carried out by the pharmaceutical industry and scientific groups.

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We contribute to the development of multi-centre clinical trials for clinical research carried out by the pharmaceutical industry and scientific groups.

At Sistemas Genómicos, we are working to provide a solution for the challenges posed by the pharmaceutical sector and the scientific world. Clinical research is becoming more expensive and more complex, meaning we have to work on multi-centre clinical trials.

Why choose Sistemas Genómicos?

CLINICAL SENSITIVITY

Our team is made up of doctors and molecular biology experts. We are pioneers in implementing NGS for clinical diagnosis.

EXPERIENCE

We have over 20 years’ experience in genomics and 50 years’ in precision diagnosis.

BIOINFORMATICS
  • GeneSystems©: Cloud computing platform for analysing massive sequencing.
  • DBNLVar: database of rare disease variants.
MEDICAL TEST GUIDES
  • Somatic mutations with digital PCR
  • Gene sequencing using Sanger or NGS
  • Gene panel via NGS
  • Whole exome or genome
  • Tailor-made adaptation of the tests for each project
CUTTING-EDGE TECHNOLOGY
  • Sanger Sequencer
  • Array Platforms
  • Next-Generation sequencing platforms
  • Digital PCR platform

Accreditations

 

We can clear up any doubts

Here at Sistemas Genómicos, we provide you will all our knowledge to help you.

Personalised Services

We provide personalised analytical solutions for our specialisation areas.