The Illumina Genome Network (IGN) offers highly accurate, complete human whole-genome sequencing services, giving researchers the clearest picture of the genome. IGN provides affordable end-to-end research solutions with the largest global install base and the capability to perform human whole-genome sequencing services quickly and confidently.
As genome sequencing becomes more accessible, the ability to study the entire human genome accelerates opportunities for discovery. Results from the ENCODE project reveal that many DNA variants previously associated to disease lie outside of the coding regions of genomic DNA. This knowledge, combined with easy access to IGN sequencing services, empowers researchers to discover novel links between genetic variations and human disease.