We offer various applications in terms of human genetics and sequencing.
Sequencing services are only available in connection with a subsequent bioinformatic data analysis.
Provides comprehensive high-resolution genetic information.
Provides information of protein-coding regions (exons) in human genomes. This allows the identification of protein-altering genetic variants at a fraction of the cost of whole-genome sequencing.
Allows quantification of transcripts to track changes in gene expression profiles, post-translational modifications, SNPs or mutations with changing conditions.
Focuses on sets of specific genes to identify diagnostically and prognostically relevant variants promoting a specific phenotype.