Infinium Multi-Ethnic EUR/EAS/SAS-8 Kit

A cost-effective array for understanding complex disease in diverse human populations, focused on European, East Asian, and South Asian populations. Read More...
Select Product(s)

Infinium Multi-Ethnic EUR/EAS/SAS-8 v1.0 Kit (16 samples)

20001100

Price
 
 

Infinium Multi-Ethnic EUR/EAS/SAS-8 v1.0 Kit (48 samples)

20001101

Price
 
 

Infinium Multi-Ethnic EUR/EAS/SAS-8 v1.0 Kit (96 samples)

20001102

Price
 
 

Infinium Multi-Ethnic EUR/EAS/SAS-8 v1.0 Kit (384 samples)

20001103

Price
 
 

Infinium Multi-Ethnic EUR/EAS/SAS-8+ v1.0 Kit (16 samples)

20001104

Infinium Multi-Ethnic EUR/EAS/SAS-8+ v1.0 Kit (48 samples)

20001105

Infinium Multi-Ethnic EUR/EAS/SAS-8+ v1.0 Kit (96 samples)

20001106

Infinium Multi-Ethnic EUR/EAS/SAS-8+ v1.0 Kit (384 samples)

20001107

Product Highlights

The Infinium Multi-Ethnic EUR/EAS/SAS-8 Kit provides a multi-purpose, multi-ethnic genotyping array focused on European, East Asian, and South Asian populations. With > 1.4 million expertly selected markers, it enables identification of genetic associations with common and rare traits, providing insight to epidemiologists, health care researchers, population geneticists, and genomic researchers.

Expert-selected content

This kit combines expertly selected markers and content from the most popular Illumina commercial arrays with the most current genomic information. Researchers can detect both common and rare variants across European, East Asian, and South Asian populations and impute variants in a vast number of subpopulations.

Maximized imputation accuracy

Consortium partners developed content for this multi-ethnic EUR/EAS/SAS genotyping array using tagging strategies with the power to perform more effective association studies in European, East Asian, and South Asian populations. The novel algorithm selects population-specific and transethnic tag SNPs that maximize imputation accuracy, as imputation has become a standard practice in the interpretation of genotyping data and allows for more accurate statistical inference of genotypes not directly genotyped.

Learn More About Human Genotyping

Specifications

Method-Specific Workflow Example

 

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