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Service

This section provides basic information about Service

DNA Analysis (GWAS, DMET)

Overview

DNA Link, Inc., the only service provider which is officially authorized by both Affymetrix and Agilent as a Certified Service Provider (CSP) in Korea, offers a wide range of SNP and expression profiling service. DNA Link guarantees the highest quality service through systematic quality control according to CSP standards since 2006. Moreover, DNA Link’s research team is very experienced with knowhow from performing many national projects and services, including analysis of more than 50,000 arrays.

Example for workflow & requirement

Genome wide Human SNP Array 6.0

  • Benefit
  • Being the most widely used SNP array in Korea, SNP 6.0 is a 1.8M array which contains 906,600 SNP probes and 946,000 non-polymorphic probes, and enables SNP and CNV analysis simultaneously.

  • Workflow
  • Sample requirement
  • DNA Amount: 500ng
    DNA Qualification: 260/280 1.8~2.0, 260/230 ratio of over 1.5, (by gel image) no RNA, no degradation

  • Turnaround timew
  • DNA QC: 2~3 days
    5 days for 48 arrays



Axiom® Genome-Wide Human Arrays

  • Benefit
  • Axiom® Genome-Wide Human Arrays is comprised of validated SNP contents from 800 million SNPs database of 1000 genome project, HapMap project, and dbSNP, which will maximize the efficiency of the experiment. Custom array production is also available

  • Workflow
  • Sample requirement
  • DNA Amount: 200ng
    DNA Qualification: 260/280 1.8~2.0, 260/230 ratio of over 1.5, (by gel image) no RNA, no degradation

  • Turnaround timew
  • DNA QC: 2~3 days
    5 days for 96 arrays



DMET Plus Assay

  • Benefit
  • Being the first array to be compromised of contents mainly associated with drug metabolism, DMET (Drug Metabolizing Enzymes and Transporters) Plus Panel can be applied for many fields, such as pharmacogenetics and clinical studies

  • Workflow
  • Sample requirement
  • DNA Amount: 1200ng
    DNA Qualification: 260/280 1.8~2.0, 260/230 ratio of over 1.5, (by gel image) no RNA, no degradation

  • Turnaround timew
  • DDNA QC: 2~3 days
    5 days for 48 arrays



Genome-Wide Genotyping for Human Disease Research

Affymetrix is a leading provider of microarray solutions for targeted and genome-wide applications. Our powerful portfolio includes arrays, reagents, instruments, and informatics tools that enable you to detect common and rare single nucleotide polymorphisms (SNPs), copy number variants, and other genetic variations that can contribute to complex diseases.

Targeted Genotyping Analysis for Human Disease Research

With target genotyping solutions, you can genotype specific sets of targeted SNPs to uncover the basis of complex human and animal genetics.

Agrigenomics Solutions

Flexible optimized solutions provide breeders and researchers with powerful cost-effective genotyping tools to identify, validate, and screen complex genetic traits for leveraging the highest economic value of the herd or plant. Our portfolio of robust, highly reproducible, and scalable products facilitates marker-trait associations, GWAS, and QTL analyses–all of which fast track your genomic selection programs. Our comprehensive solutions for animal and plant genotyping offer the ability to customize your genotyping arrays for commercially significant species.

Model Organisms and Companion Animals

Model organisms and companion animals are valuable for comparative genomics research, evolutionary biology, and continue to play a critical role in deciphering the molecular mechanisms underlying human disease and agricultural crop improvement.

Molecular Cytogenetics

Join the resolution revolution. Get performance that exceeds industry guidelines for specificity, sensitivity, and resolution. Be confident in identifying chromosomal aberrations.

OncoScan™ FFPE Assay Kits

Genome-wide copy number in 48 hours

Arrays and Assays

Copy Number Analysis

Affymetrix provides a suite of products designed for researchers exploring the role of copy number in human disease. The Genome-Wide Human SNP Array 6.0 provides copy number estimates for more than 1.8 million markers on a single array, more than half of which are non-polymorphic probes selected for their linear response to copy number and genomic position.

DMET Plus Solution

The broadest coverage, single pharmacogenetic assay that enables the most rapid genetic analysis of the involvement of metabolic pathways in drug metabolism.

Arrays and Assays

Cartridges

Resequencing Analysis

Focus your research with GeneChip® CustomSeq® Resequencing Arrays—the most efficient and cost-effective way to quickly interrogate large amounts of sequence in a single experiment.