This system is ideal for fine mapping, screening, candidate gene or QTL analysis and microarray replication studies. The SNPlex™ Genotyping System enables the simultaneous genotyping of up to 48 SNPs (single nucleotide polymorphisms) against a single biological sample. The system detects up to 4500 SNPs in parallel in 15 minutes.
DNAVision, as an ABI certified Service Provider, offers a complete range of supporting services from the study design and sample processing until data analyses and genotype reporting.
Official service provider for SNPlex genotyping (Applied Biosystems)
Brochure: SNP genotyping at DNAVision
SNPlex™ Genotyping System is addressed to the need for accurate genotyping data, high sample throughput, study design flexibility and cost efficiency. The system uses oligonucleotide ligation/polymerase chain reaction and capillary electrophoresis to analyze bi-allelic single nucleotide polymorphism genotypes. It is well suited for single nucleotide polymorphism genotyping efforts in which throughput and cost efficiency are essential.
SNPlex™ offers a high degree of flexibility and scalability, allowing the selection of custom-defined sets of SNPs for medium- to high-throughput genotyping projects. It is therefore suitable for a broad range of study designs.
Definitively, SNPlex™ Genotyping System is an efficient and reliable tool for a broad range of genotyping applications, supported by applications for study design, data analysis, and data management.
Samples must be submitted in a specified sample layout: concentration of 37 ng/µl and 10 µl/pool minimum.
