The new Affymetrix Genome-Wide Human SNP Array 6.0 features 1.8 million genetic markers, including more than 906,600 single nucleotide polymorphisms (SNPs) and more than 946,000 probes for the detection of copy number variation. The SNP Array 6.0 is the only platform with analysis tools to truly bridge copy number and association, including a new, high-resolution reference map and a copy number polymorphism (CNP) calling algorithm developed by the Broad Institute. The SNP Array 6.0 demonstrates industry-leading performance and represents more genetic variation on a single array than any other product, providing maximum panel power and the highest physical coverage of the genome.
Study indepth drug metabolism with the DMET™ Plus Premier Pack. The DMET Plus system standardizes drug metabolism studies and enables faster discovery of genetic variation associated with drug response.
Affymetrix microarray solutions for targeted and genome-wide applications enable you to detect common and rare single nucleotide polymorphisms (SNPs), copy number variants, and other genetic variations that can contribute to complex diseases.
The CytoScan™ HD Cytogenetics Solution, offers the most comprehensive coverage available to for Human Cytogentic analysis. Traditional cytogenetics techniques such as karyotyping and fluorescent in situ hybridization (FISH) have been used to study chromosomal abnormalities for decades. These techniques are limited to only providing low-resolution copy number information based on qualitative visualization. Designed to empower next-generation cytogenetic studies, the CytoScan® HD Cytogenetics Solution provides a genome-wide approach that enables high-resolution DNA copy number analysis to detect gains, losses, loss of heterozygosity (LOH), regions identical-by-descent, and uniparental isodisomy (UPD) on a single array.
The most comprehensive and relevant coverage of constitutional and cancer genes on a single array
coverage of all 36,000 RefSeq genes including 12,000 OMIM, all ISCA constitutional regions, and Sanger cancer genes
High-density genotype-able SNPs
for low-level mosaicism visualization, loss of heterozygosity (LOH) detection, copy number change confirmation, and genotypes
Performance that exceeds community guidelines
specificity, sensitivity, and resolution across the genome
Complete solution that saves time and money
streamlined protocols, optimized assay performance, bundled reagents, easy-to-use software, DVD and laboratory-based training
Proven ChAS Software with genotypes
intuitive, graphical, and streamline analysis software
Highest performance with the broadest range of sample types
blood, bone marrow, buccal saliva, fresh and frozen tissue, fresh and cultured cells, and more
The complete cytogenetics research solution
Used in combination with the GeneChip® Instrument System, the next-generation Affymetrix CytoScan® HD Cytogenetics Solution provides everything you need to do cytogenetics research.
