genome sequencing and informatics solutions
At intelliseq, we understand that in-depth data analysis and interpretation lies at the very heart of successful genome-wide research. Our expertise arises from over a trillion bases analyzed, originating from DNA-seq, RNA-seq and ChIP-seq.
Our goal is to support the scientific research and medical diagnostics with providing the comprehensive solutions of high-throughput DNA sequencing. We offer e.g. whole exome/genome sequencing and gene panels sequencing (up to 300 genes).
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Latest Blog Posts
A case for GRCh38 – FRG1 gene
Recently we aligned some of our samples’ reads to both GRCh37 and GRCh38 reference genomes and compared the results of our...
Intelliseq switched to Grch38 human genome reference
After initial testing we decided to switch to Grch38+ALT+DECOY+HLA genome reference. We gathered all required resources and translated some from Grch37...