Sapio Sciences offers the Exemplar Analytics 4.0.8, the first commercial solution, outside of Illumina, to provide CNV analysis for the Illumina family of arrays. Copy number variation analysis is a powerful and widely used method for identifying insertions and deletions in the genome. The identification of these chromosomal alterations is critical in understanding cancer as well as other serious diseases.
The tool offers support of all Illumina DNA Analysis BeadChips from the Human-1 to Human1M BeadChip; principal component analysis for admixture corrections; proper Allele counting of Hemizygous SNPs; complete update of the annotations database with current information from dBSNP, Entrez gene, and gene ontology; multi-processor support for permutation corrections on statistics; full Support of copy number analysis for the Affymetrix 10K-500K, 5.0 and 6.0 arrays
Filed Under: Drug Discovery
