Infinium Multi-Ethnic Global-8 Kit

A cost-effective array for understanding complex disease in diverse human populations.Read More...
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Fixed Content

Infinium Multi-Ethnic Global-8 v1.0 Kit (16 samples)

WG-316-1001

Infinium Multi-Ethnic Global-8 v1.0 Kit (48 samples)

WG-316-1002

Infinium Multi-Ethnic Global-8 v1.0 Kit (96 samples)

WG-316-1003

Infinium Multi-Ethnic Global-8 v1.0 Kit (384 samples)

WG-316-1004


Add-On Content

Infinium Multi-Ethnic Global-8+ v1.0 Kit (16 samples)

WG-316-1011

Infinium Multi-Ethnic Global-8+ v1.0 Kit (48 samples)

WG-316-1012

Infinium Multi-Ethnic Global-8+ v1.0 Kit (96 samples)

WG-316-1013

Infinium Multi-Ethnic Global-8+ v1.0 Kit (384 samples)

WG-316-1014

Product Highlights

The Infinium Multi-Ethnic Global-8 Kit provides a true multi-purpose, multi-ethnic genotyping array. With > 1.7 million expertly selected markers, it enables identification of genetic associations with common and rare traits, providing insight across diverse populations 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 the most commonly studied 5 major super-populations and impute variants in a vast number of subpopulations.

Maximized imputation accuracy

Consortium partners developed content for this multi-ethnic global genotyping array using tagging strategies with the power to perform more effective association studies in diverse 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.

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规格

产品比较

Infinium Multi-Ethnic Global-8 Kit Infinium Omni2.5-8 Kit Infinium Omni5-4 Kit
变异种类 拷贝数变异(CNV), 插入缺失, 生殖系变异, 单核苷酸多态性(SNP), 结构变异 拷贝数变异(CNV), 插入缺失, 生殖系变异, 单核苷酸多态性(SNP), 结构变异 拷贝数变异(CNV), 插入缺失, 生殖系变异, 单核苷酸多态性(SNP), 结构变异
技术 微阵列芯片 微阵列芯片 微阵列芯片
方法 全基因组基因分型芯片 全基因组基因分型芯片 全基因组基因分型芯片
标记物数量 固定标记物:1,779,819
定制标记物扩展容量:多达245,000
固定标记物:2,338,671 固定标记物:4,284,426
核酸类型 DNA DNA DNA
物种类别 人类 人类 人类
特殊的样本类型 FFPE组织 FFPE组织
系统兼容性 iScan