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 signs a collaboration agreement with Objetivo Diagnóstico
Objetivo Diagnóstico and Dreamgenics have signed a framework agreement of institutional collaboration to promote the genetic diagnosis of rare diseases, as well as to develop research projects.
Rare diseases: more refined diagnostics, more specific treatments
Yesterday, February 23, we participated in the IMMeeting organized by IMMédico magazine to talk about rare diseases, their diagnosis and treatment, together with
APADA Seminar: Hearing Loss and Genetics
Hypoacusis is the loss of hearing capacity, to a lesser or greater degree, which may be caused by environmental or genetic causes.