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.
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 and APACI sign a Framework Collaboration Agreement to promote genetic diagnosis of congenital heart disease
APACI and Dreamgenics have signed a framework agreement for institutional collaboration to promote genetic diagnosis of congenital cardiovascular diseases, as well as to develop projects of
Considerations for the correct identification of CNVs from exome sequencing
CNVs (Copy Number Variations) are a type of structural variants of submicroscopic size, such as deletions, duplications, insertions, inversions, and translocations, which involve a change
How many replicates are needed for an RNA-Seq experiment?
Since its emergence just over a decade ago, we have witnessed how RNA-Seq technology has revolutionized our understanding of the transcriptome. This methodology