CD Genomics, a global leader in the supply of Next Generation Sequencing related services, recently launched its SNaPshot Multiplex System. By using CD Genomics’ SNaPshot Multiplex System method, the SNP genotyping results are efficiently obtained and robust, reproducible analyses of multiplexed samples are also easily processed.
The SNaPshot Multiplex System is a primer extension-based method for genotyping known SNP positions through the automated DNA analyzer invented by Applied Biosystems. Through its multiplexing capability, up to 10 SNPs can be analyzed in a single reaction by using unlabeled, user-defined primers. SNPs can be interrogated regardless of their position on the chromosome or separation from a neighboring SNP locus. With it, over 20,000 SNP genotypes per day can be analyzed by researchers.
SNPs have been identified in all genomes and can be used for a large number of analyses, for example, studying mutations implicated in various cancers, genetic disease research, mitochondrial DNA investigations, scrapie susceptibility in sheep, loss of heterozygosity, assessing performance in food animal production, and even differentiating drug and non-drug forms of Cannabis.
CD Genomics is planning further academic partnerships and extensive marketing moves, applying its SNaPshot for genotyping 1-100 SNPs and up to thousands of samples. The system offers researchers high accuracy and sensitive allele-frequency detection. It’s consistence and easy to use.
Dianna Gellar, CSO of CD Genomics, said: “We helps researchers ensure robust and reproducible analyses of multiplexed samples with our system. And We want to make specialized, validated workflow to guarantee basic or customized research.”
To find out more, visit https://www.cd-genomics.com/SNaPshot.html.
About CD Genomics
CD Genomics was established in 2004, we are aiming at providing the research community with high quality Next Generation Sequencing, high throughput microarray services. Due to the demand for our services has being increased; CD Genomics has already updated its technology platform to mainstream NGS and microarray instruments. At present, our senior bioinformaticians have ever viewed more than ten thousand of trace files and accumulated abundant experience with our Illumina HiSeq2000/2500, Illumia Miseq, Ion Torrent PGM, PacBio RS and ABI 3730/3730XL analyzers. We continue to work hard to offer you the same dependable services to pharmaceutical and biotech companies, as well as academia and government agencies for the purpose of satisfying all your sequencing or array needs.
Company Name: CD Genomics
Contact Person: Dianna Gellar
Email: Send Email
Address:45-1 Ramsey Road
State: New York
Country: United States