A targeted approach
to genetic disorders
Our broad portfolio of tests allows us to study different genetic diseases with approaches tailored to each case
Genetic studies in nine medical specialties
We offer targeted exomes that encompass the genes of clinical interest in each pathology. In addition, we perform whole exome analysis for complex cases.
Our targeted exomes include genes associated or potentially associated, with sufficient scientific evidence, to the development of each disease and have been selected using clinical databases such as Orphanet, OMIM, HGMD and GeneReviews, among others, and disease-specific databases, if available.
We are experts in bioinformatics analysis of NGS data.
We work with our own pipelines and our Genome One software, which is CE-IVD marked.
We have more than 12 years of experience in the analysis of NGS data and we are specialized in genomics and transcriptomics.
NGS sequencing
We use laboratory equipment and reagents with CE-IVD marking.
We offer our customers a comprehensive service, including DNA and RNA extraction, quality control, library preparation and NGS sequencing on MGI or Illumina platforms, depending on their preferences.
Blog & News
Dreamgenics adds NGS sequencing equipment to its laboratory
We are very pleased to announce our recent collaboration with MGI to bring the internalization of the NGS sequencing service with the
Paula Martínez, new Junior Bioinformatician
We welcome Paula Martinez to Dreamgenics, who joins our team as a new Junior Bioinformatician. Paula has a degree in Engineering
Studying human genetic diseases: what massive sequencing can offer us.
In the latest issue of IMMédico Magazine, our bioinformatics team has published an article on the development of Next-Generation Sequencing technologies.