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Data Sheet
Axiom™
myDesign™
Targeted Genotyping Array Plates
Targeted genotyping, tailored for your study
Axiom™
myDesign™
Targeted Genotyping (TG) Array Plates
are fully customizable panels that can be optimized with
the most relevant genomic markers for your fine mapping,
candidate gene, and SNP validation studies, as well as for
developing your own focused panels for routine screening.
Axiom myDesign TG Array Plates enable you to:
n	 Easily select relevant SNPs from our database of 11
million validated common and rare variants
n	 Create panels of 1,500 to 500,000 markers per sample
n	 Generate rapid, robust results
n	 Conduct genome-wide association studies (GWAS)
and candidate gene studies on the same platform
n	 Receive your array more quickly than any custom array
on the market
Introduction
Whether exploring interesting regions after your genome-wide
association study, validating novel SNPs from your sequencing
experiment, or ramping up your candidate gene project, Axiom
myDesign TG Array Plates are the newest innovation from
Affymetrix to accelerate your focused genotyping studies.
Based on the universal workflow of the Axiom™
Genotyping
Solution, Axiom myDesign TG Array Plates offer the confidence
of validated genomic content and unprecedented flexibility to
design an optimal panel for your study.
Axiom myDesign TG Array Plates provide:
n	 The most comprehensive content – Tailor your custom
arrays using the Axiom™
Genomic Database, the world’s
largest database of validated genomic content from the
human genome spanning four major populations (CEU,
JPT, CHB, and YRI). The database contains more than 11
million rare and common variants from sources such as
the International HapMap Project, the 1000 Genomes
Project, the NHGRI Database of Published Associations,
and other initiatives.
n	 Uniquely relevant markers – Choose the most relevant
markers based on population, linkage disequilibrium (LD,
measured by r2
), and minor allele frequency (MAF) to
maximize statistical power for the study. Genomic markers
are further classified by SNP type, biological process, or
previous disease association GWAS.
n	 Superior results – Have confidence in your data with
millions of validated markers. Each variant has been
extensively validated in a large number of biological samples
to ensure that the SNP is not due to sequencing error, the
minor allele can be reliably detected, and has undergone
rigorous functional testing to ensure highly reliable and
reproducible performance. Data quality was assessed against
the HapMap 270 diversity panel to confirm call rate, sample
pass rate, concordance, and reproducibility.
n	 Unmatched scalability – Create fully customized panels
containing 1,500 to 500,000 markers using validated content
from Affymetrix, or submit novel target sequence from
other sources. This industry-leading scalability provides more
options to maximize genetic coverage across the genome or
within specific gene regions to support SNP validation, fine
mapping, or candidate gene studies.
n	 Accelerated discovery – Process more than 750
samples per week using the fully automated workflow
based on the Axiom™
2.0 Reagent Kit and the GeneTitan®
Multi-Channel Instrument.
Easy to select, easy to design
Designing an Axiom myDesign TG Array Plate is easy. Register
online at www.affymetrix.com/mydesign to access the Axiom
Design Center, your gateway to SNP selection and array design
using the Axiom Genomic Database.
All design requests are submitted online, and the Affymetrix
Bioinformatics Services team will help you create your custom
Axiom panel. You can submit gene, region, sequence, or probe
ID. The design and ordering process is outlined in detail in
the Axiom™
myDesign™
Array Plate Design Guide, available at
www.affymetrix.com.
www.affymetrix.com Please visit our website for international distributor contact information.
For Research Use Only. Not for use in diagnostic procedures.
P/N DNA00627 Rev. 1
©Affymetrix, Inc. All rights reserved. Affymetrix®
, Axiom™
, Command Console®
, DMET™
, GeneAtlas™
, GeneChip®
, GeneChip-compatible™
, GeneTitan®
, Genotyping Console™
, myDesign™
, NetAffx®
,
OncoScan™
, Powered by Affymetrix™
, Procarta®
, and QuantiGene®
are trademarks or registered trademarks of Affymetrix, Inc. All other trademarks are the property of their respective owners.
Products may be covered by one or more of the following patents: U.S. Patent Nos. 5,445,934; 5,744,305; 5,945,334; 6,140,044; 6,399,365; 6,420,169; 6,551,817; 6,733,977; 7,629,164; 7,790,389
and D430,024 and other U.S. or foreign patents. Products are manufactured and sold under license from OGT under 5,700,637 and 6,054,270.
Affymetrix, Inc. Tel: +1-888-362-2447  Affymetrix UK Ltd. Tel: +44-(0)-1628-552550  Affymetrix Japan K.K. Tel: +81-(0)3-6430-4020
Panomics Products Tel: +1-877-PANOMICS www.panomics.com  USB Products Tel: +1-800-321-9322 www.usb.affymetrix.com
Table 2: Validated markers by biological category.
Marker category No. of validated markers
By marker type
Coding SNPs (cSNPs) 88,922
	 Synonymous cSNPs 43,860
	 Non-synonymous cSNPs 52,251
Splicing and untranslated regions (UTR) 111,001
Genic 3,991,806
miRNA/mtDNA 405
Chromosome X/chromosome Y 249,608/2,647
Insertions/deletions (in/dels) 34,708
By biological process and disease
Major histocompatibility complex (MHC) 22,148
Drug metabolizing genes/ADMET 50,455
Inflammation and immunity pathway 57,922
Cardiovascular 68,479
NHGRI disease-associated 3,299
Cancer 107,422
Table 3: Markers by commercially available panel.
Panel
No. of
validated
markers
Axiom™
Genome-Wide ASI Array Plate 600,307
Axiom™
Genome-Wide CEU Array Plate 587,352
Affymetrix®
Genome-Wide Human SNP Array 5.0 384,766
Affymetrix®
Genome-Wide Human SNP Array 6.0 769,824
Illumina Infinium Human660W-Quad BeadChip 470,852
Illumina Infinium Human1M-Duo BeadChip 811,252
Illumina HumanOmniExpress BeadChip 586,993
Illumina HumanOmni1 BeadChip 779,796
Ordering information
Part
number
Description Details
Axiom™
myDesign™
Targeted Genotyping Array Plates
000799 Axiom™ myDesign™ TG Array Plate, 1x96 format Includes one 96-array plate of one array type containing 1,500 to 500,000 markers per sample
Axiom™
Reagent Kits
901758 Axiom™
2.0 Reagent Kit Includes all reagents (except isopropanol) to process 96 gDNA samples
901606 GeneTitan®
Consumables Kit Includes GeneTitan®
plastic consumables to process one 96-array plate
Axiom™
Services
0000740 Axiom™
Genotyping Services
Sample processing and data generation services for gDNA samples (minimum 1,000 samples) using the
Axiom Genotyping Solution
*Reagent kits do not include Beckman plastic consumables required to run the assay on the Beckman Biomek®
FXP
Target Prep Express System.
Table 1: Markers in the Axiom™
Genomic Database (millions).
Total polymorphic markers by population
Total markers
by population
Total no. of
markers by MAF
No. of
validated markers
No. of taggable
markers with r2
>0.8
CEU
Rare (0<MAF<5%)
6.11
1.67 1.46 0.21
Common (MAF≥5%) 4.44 3.26 1.18
JPT + CHB
Rare (0<MAF<5%)
5.63
1.61 1.44 0.17
Common (MAF≥5%) 4.02 2.98 1.04
YRI
Rare (0<MAF<5%)
8.71
2.73 2.43 0.3
Common (MAF≥5%) 5.99 4.7 1.29
Total 11.0 8.8 2.2

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Axiom™ myDesign™ Targeted Genotyping Array Plates

  • 1. Data Sheet Axiom™ myDesign™ Targeted Genotyping Array Plates Targeted genotyping, tailored for your study Axiom™ myDesign™ Targeted Genotyping (TG) Array Plates are fully customizable panels that can be optimized with the most relevant genomic markers for your fine mapping, candidate gene, and SNP validation studies, as well as for developing your own focused panels for routine screening. Axiom myDesign TG Array Plates enable you to: n Easily select relevant SNPs from our database of 11 million validated common and rare variants n Create panels of 1,500 to 500,000 markers per sample n Generate rapid, robust results n Conduct genome-wide association studies (GWAS) and candidate gene studies on the same platform n Receive your array more quickly than any custom array on the market Introduction Whether exploring interesting regions after your genome-wide association study, validating novel SNPs from your sequencing experiment, or ramping up your candidate gene project, Axiom myDesign TG Array Plates are the newest innovation from Affymetrix to accelerate your focused genotyping studies. Based on the universal workflow of the Axiom™ Genotyping Solution, Axiom myDesign TG Array Plates offer the confidence of validated genomic content and unprecedented flexibility to design an optimal panel for your study. Axiom myDesign TG Array Plates provide: n The most comprehensive content – Tailor your custom arrays using the Axiom™ Genomic Database, the world’s largest database of validated genomic content from the human genome spanning four major populations (CEU, JPT, CHB, and YRI). The database contains more than 11 million rare and common variants from sources such as the International HapMap Project, the 1000 Genomes Project, the NHGRI Database of Published Associations, and other initiatives. n Uniquely relevant markers – Choose the most relevant markers based on population, linkage disequilibrium (LD, measured by r2 ), and minor allele frequency (MAF) to maximize statistical power for the study. Genomic markers are further classified by SNP type, biological process, or previous disease association GWAS. n Superior results – Have confidence in your data with millions of validated markers. Each variant has been extensively validated in a large number of biological samples to ensure that the SNP is not due to sequencing error, the minor allele can be reliably detected, and has undergone rigorous functional testing to ensure highly reliable and reproducible performance. Data quality was assessed against the HapMap 270 diversity panel to confirm call rate, sample pass rate, concordance, and reproducibility. n Unmatched scalability – Create fully customized panels containing 1,500 to 500,000 markers using validated content from Affymetrix, or submit novel target sequence from other sources. This industry-leading scalability provides more options to maximize genetic coverage across the genome or within specific gene regions to support SNP validation, fine mapping, or candidate gene studies. n Accelerated discovery – Process more than 750 samples per week using the fully automated workflow based on the Axiom™ 2.0 Reagent Kit and the GeneTitan® Multi-Channel Instrument. Easy to select, easy to design Designing an Axiom myDesign TG Array Plate is easy. Register online at www.affymetrix.com/mydesign to access the Axiom Design Center, your gateway to SNP selection and array design using the Axiom Genomic Database. All design requests are submitted online, and the Affymetrix Bioinformatics Services team will help you create your custom Axiom panel. You can submit gene, region, sequence, or probe ID. The design and ordering process is outlined in detail in the Axiom™ myDesign™ Array Plate Design Guide, available at www.affymetrix.com.
  • 2. www.affymetrix.com Please visit our website for international distributor contact information. For Research Use Only. Not for use in diagnostic procedures. P/N DNA00627 Rev. 1 ©Affymetrix, Inc. All rights reserved. Affymetrix® , Axiom™ , Command Console® , DMET™ , GeneAtlas™ , GeneChip® , GeneChip-compatible™ , GeneTitan® , Genotyping Console™ , myDesign™ , NetAffx® , OncoScan™ , Powered by Affymetrix™ , Procarta® , and QuantiGene® are trademarks or registered trademarks of Affymetrix, Inc. All other trademarks are the property of their respective owners. Products may be covered by one or more of the following patents: U.S. Patent Nos. 5,445,934; 5,744,305; 5,945,334; 6,140,044; 6,399,365; 6,420,169; 6,551,817; 6,733,977; 7,629,164; 7,790,389 and D430,024 and other U.S. or foreign patents. Products are manufactured and sold under license from OGT under 5,700,637 and 6,054,270. Affymetrix, Inc. Tel: +1-888-362-2447  Affymetrix UK Ltd. Tel: +44-(0)-1628-552550  Affymetrix Japan K.K. Tel: +81-(0)3-6430-4020 Panomics Products Tel: +1-877-PANOMICS www.panomics.com  USB Products Tel: +1-800-321-9322 www.usb.affymetrix.com Table 2: Validated markers by biological category. Marker category No. of validated markers By marker type Coding SNPs (cSNPs) 88,922 Synonymous cSNPs 43,860 Non-synonymous cSNPs 52,251 Splicing and untranslated regions (UTR) 111,001 Genic 3,991,806 miRNA/mtDNA 405 Chromosome X/chromosome Y 249,608/2,647 Insertions/deletions (in/dels) 34,708 By biological process and disease Major histocompatibility complex (MHC) 22,148 Drug metabolizing genes/ADMET 50,455 Inflammation and immunity pathway 57,922 Cardiovascular 68,479 NHGRI disease-associated 3,299 Cancer 107,422 Table 3: Markers by commercially available panel. Panel No. of validated markers Axiom™ Genome-Wide ASI Array Plate 600,307 Axiom™ Genome-Wide CEU Array Plate 587,352 Affymetrix® Genome-Wide Human SNP Array 5.0 384,766 Affymetrix® Genome-Wide Human SNP Array 6.0 769,824 Illumina Infinium Human660W-Quad BeadChip 470,852 Illumina Infinium Human1M-Duo BeadChip 811,252 Illumina HumanOmniExpress BeadChip 586,993 Illumina HumanOmni1 BeadChip 779,796 Ordering information Part number Description Details Axiom™ myDesign™ Targeted Genotyping Array Plates 000799 Axiom™ myDesign™ TG Array Plate, 1x96 format Includes one 96-array plate of one array type containing 1,500 to 500,000 markers per sample Axiom™ Reagent Kits 901758 Axiom™ 2.0 Reagent Kit Includes all reagents (except isopropanol) to process 96 gDNA samples 901606 GeneTitan® Consumables Kit Includes GeneTitan® plastic consumables to process one 96-array plate Axiom™ Services 0000740 Axiom™ Genotyping Services Sample processing and data generation services for gDNA samples (minimum 1,000 samples) using the Axiom Genotyping Solution *Reagent kits do not include Beckman plastic consumables required to run the assay on the Beckman Biomek® FXP Target Prep Express System. Table 1: Markers in the Axiom™ Genomic Database (millions). Total polymorphic markers by population Total markers by population Total no. of markers by MAF No. of validated markers No. of taggable markers with r2 >0.8 CEU Rare (0<MAF<5%) 6.11 1.67 1.46 0.21 Common (MAF≥5%) 4.44 3.26 1.18 JPT + CHB Rare (0<MAF<5%) 5.63 1.61 1.44 0.17 Common (MAF≥5%) 4.02 2.98 1.04 YRI Rare (0<MAF<5%) 8.71 2.73 2.43 0.3 Common (MAF≥5%) 5.99 4.7 1.29 Total 11.0 8.8 2.2