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Axiom® Genome-Wide Population-Optimized Human Arrays

Axiom® Genome-Wide Population-Optimized Human Arrays are genotyping panels that offer the best genetic coverage of rare and common variants for efficient genome-wide disease association studies.

Part # Description Unit Size Your Price (USD)
Qty
901608
Axiom® Genome-Wide CEU 1 Array Plate
Includes one 96-array Axiom Genome-Wide CEU 1 Plate    Please Inquire
901640
Axiom® Genome-Wide ASI 1 Array Plate
Includes one 96-array Axiom Genome-Wide ASI 1 Plate    Please Inquire
901764
Axiom® Genome-Wide CHB 1 Array Plate
Includes one 96-array Axiom Genome-Wide CHB 1 Plate    Please Inquire
901842
Axiom® Genome-Wide CHB 2 Array Plate
Includes one 96-array Axiom Genome-Wide CHB 2 Plate    Please Inquire
901843
Axiom® Genome-Wide CHB 1 & CHB 2 Array Set Bundle
Sufficient for 96 gDNA samples, includes:
•One Axiom GW CHB 1 Array Plate
•One Axiom GW CHB 2 Array Plate
•Two Axiom 2.0 Reagent kits
•Two GeneTitan? Consumables Kits   
Please Inquire
901788
Axiom® Genome-Wide PanAFR Genotyping Bundle
Sufficient for 96 gDNA samples, includes:
•One Axiom GW PanAFR Array Plate Set
•Three Axiom 2.0 Reagent kits
•Three GeneTitan? Consumables Kits   
Please Inquire
901606
Axiom® GeneTitan® Consumables Kit
Contains all GeneTitan® Instrument consumables required to process one Axiom® Array Plate    Please Inquire
901758
Axiom® 2.0 Reagent Kit
Includes all reagents (except isopropanol) to process 96 reactions    Please Inquire
     

Axiom® Genome-Wide Population-Optimized Human Arrays are genotyping panels that offer the best genetic coverage of rare and common variants for genome-wide disease association studies.

Don't see what you're looking for? Learn how to create an Axiom® myDesign™ Array tailored for your study >

Benefits of Axiom Genome-Wide Population-Optimized Arrays:

Each array plate was designed to achieve ~90% genomic coverage (r2 >0.8) in each target population, while covering markers with MAF of 1-5% in areas such as:

  • Critical biological categories (e.g., coding SNPs)
  • Biological processes (e.g., drug metabolizing genes)
  • Disease categories (e.g., cardiovascular disease, cancer, immunity/inflammation, MHC, and CNS)
  • Common and rare SNPs and insertions/deletions (indels) from the International HapMap Project, 1000 Genomes Project, and published disease associations
  • Genotype-tested genomic content proven to give informative and reliable results
  • Markers preselected for coverage in critical biological categories, such as coding SNPs, and biological pathways, such as drug metabolizing or cardiovascular genes
  • High sample pass rate, call rate, and reproducibility
  • Compatible with the Axiom® 2.0 Reagent Kit, GeneTitan® MC Instrument, automated or manual workflow, and Genotyping Console™ Software

Maximum Genome-Wide Coverage Arrays

These array plates are designed to maximize whole-genome coverage of common and rare alleles, including SNPs within 10 kb of genes.

  • Axiom® Genome-Wide CEU 1 Array Plate - The first cost-effective array to maximize coverage of rare variants (MAF >1%) for European populations
  • Axiom® Genome-Wide ASI 1 Array Plate - The first array designed to maximize genomic coverage of rare alleles (MAF >1%) of a consensus East Asian (JPT+CHB) genome
  • Axiom® Genome-Wide CHB 1 & CHB 2 Array Plate Set - Axiom Genome-Wide CHB 1 Array Plate maximizes genomic coverage of common alleles (MAF >5%) of the Han Chinese genome. Axiom Genome-Wide CHB 2 Array Plate is designed to target rare variants (MAF 2-5%) as a complement to Axiom Genome-Wide CHB 1 Array Plate. Axiom Genome-Wide CHB 1 & CHB 2 Array Set Bundle enables the most comprehensive commercially available genome-wide coverage in CHB populations.
  • Axiom® Genome-Wide PanAFR Array Plate Set - The first array to offer pan-African genomic coverage, with ≥90% genetic coverage of common and rare variants (MAF >2%) of the Yoruba (West African) genome and >85% coverage of common and rare variants (MAF >2%) of the Luhya and Maasi (East African) genomes. This array set also offers high genomic coverage (>85%) in admixed populations with West African ancestry.

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