Advanced Genomics Technology Center offers comprehensive genomic services to the biotechnology, pharmaceutical, government, and academic communities. In addition to providing the highest quality data available, our scientific team of experts will assist you in your experimental design and data analysis to optimize the value of your research. From infectious disease pathogen screening to cancer research companion diagnostics, Advanced Genomics offers a personalized approach to address your specific research needs. All microarray studies are powered by Illumina systems, the world’s most versatile platform for genetic analysis. Our scientists use this platform to provide SNP genotyping, LOH and CNV studies and gene expression analyses. Advanced Genomics also provides genetic characterization and pathogen testing services of tissue samples and cell lines.
Advanced Genomics offers the Illumina HumanOmni1-Quad BeadChip
The HumanOmni1-Quad BeadChip delivers carefully selected markers that capture the highest amount of genomic variation and the best power for genome-wide association studies (GWAS) and CNV discovery and screening. SNPs selected from all three HapMap phases capture more genomic variation and provide the best combination of power, price and throughput available for genome wide association studies (GWAS). High marker density and the fewest large gaps ensure precise CNV detection. The format of the HumanOmni1-Quad BeadChip supports simultaneous genotyping of four samples which increases throughput and decreases the per sample price. With the most up-to-date content and highest data quality, you can make more meaningful discoveries and take a faster path to publication.
• The first microarray with content from the 1,000 Genomes Project
• 11,000 validated common and rare CNVs
• More than 30,000 coding and non-synonymous SNPs
• Superior coverage of SNPs and indels