DNA - Whole Genome
Genotyping
Expression Analysis offers Illumina’s Infinium HD whole genome DNA analysis BeadChips for SNP genotyping and analysis of structural variants. Assay panels contain from 300,000 to 1,200,000 markers per specimen and accommodate 2 to 12 samples per chip and require only 200 ng to 400 ng of genomic DNA per sample. Custom content can also be added to these chips. The Infinium HD Assay procedure employs whole-genome amplification without PCR or ligation with two-step allele detection providing high call rates and accuracy.
Illumina Human1M-Duo
Illumina Human660W-Quad
Illumina HumanCytoSNP-12
The HumanOmni1-Quad BeadChip provides an unparalleled, extensive view of the genome, in a high-throughput format.
Intelligently selected SNPs 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.
Illumina HumanOmni1-Quad BeadChip
The HumanOmni2.5-Quad is the most comprehensive set of common and unexplored rare SNP content for diverse world populations.
Variation down to 2.5% minor allele frequency (MAF) - that’s 50% greater coverage of common and rare variants than any other previous array.
Illumina HumanOmni2.5-Quad BeadChip
The HumanOmni1S is a supplemental microarry, adding novel data from the first releases of the 1000 Genomes Project (1kGP) with a minor allele frequency to ~2.5%
The Human OmniExpress allows comprehensive coverage of common variants with the industry’s highest output.
Illumina The HumanOmniExpress BeadChip