SNP and CNV

SNP microarrays have become an important tool for discovering copy number variations (CNVs) that contribute to human diseases and phenotypes.

The probes on the Illumina BeadChips were chosen such that it will provide maximum coverage of the genome.

Additionally, more focus formats for validation and screening are available, either at 48-96 SNPs format (Fluidigim BioMark HD) or less (Ion Torrent PGM).

Advanced analysis is included in our service.

For orders please read the samples delivery instructions, fill and send us the electronic sample sheet.

For additional info, please contact Liat Linde, tel 04-8295452/221.