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.
RNA Sequencing
Allows quantification of transcripts to track changes in gene expression profiles, post-translational modifications, SNPs or mutations with changing conditions.
Targeted Re-Sequencing
Focuses on sets of specific genes to identify diagnostically and prognostically relevant variants promoting a specific phenotype.
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