Infinium Global Screening Array-24 Kit

The Infinium Global Screening Array-24 v3.0 BeadChip is a next-generation genotyping array for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research.Read More...
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Fixed Content

Infinium Global Screening Array-24 v3.0 Kit (48 Samples)

20030770

Infinium Global Screening Array-24 v3.0 Kit (288 Samples)

20030771

Infinium Global Screening Array-24 v3.0 Kit (1152 Samples)

20030772


Add-On Content

Infinium Global Screening Array-24+ v3.0 Kit (48 Samples)

20030773

Infinium Global Screening Array-24+ v3.0 Kit (288 Samples)

20030774

Infinium Global Screening Array-24+ v3.0 Kit (1152 Samples)

20030775

Product Highlights

全球人群内容

Infinium Global Screening Array-24 v2.0 BeadChip综合了多种族的全基因组内容、精选的临床研究变异以及用于精准医疗研究的质量控制(QC)标记。

该芯片选择了全基因组内容以获得高推断准确性,实现在千人基因组计划中的全部26种人群中最小等位基因频率>1%。临床研究内容包括已确定与疾病具有关联的变异、相关的药物基因组学标记和基于ClinVar、NHGRI、PharmGKB和ExAC数据库精选的外显子内容。质量控制内容使在大规模基因组学和筛查应用中识别和追踪样本成为可能。

广泛应用

在商业发布前就已售出可用于550多万份样本的BeadChip,该芯片的全球应用将人类疾病研究人员、医疗网络、消费者基因组学公司和基因组学服务供应商连接了起来,有助于推动发现。

广泛的临床研究应用

该芯片为疾病风险分析研究、药物基因组学研究、健康状态鉴定以及复杂疾病发现等临床研究应用提供了基因组学工具。

Global Screening Array的第3版利用了最新发布的相关的临床研究筛查标记,这些标记来自ClinVar、CPIC和PharmGKB。

随着ClinVar等主要的数据库在不断地快速添加新的变异,Illumina也会不断更新GSA检测的变异,并确保变异的相关性。发布的Infinium GSA-24 v3.0 BeadChip更新了ACMG 59基因中发现的关键变异。全世界越来越多的精准医疗研究项目正在利用这些变异来筛选人群,用于以下应用:

  • 研究ClinVar指定的“致病”和“可能致病”变异在表型发生的可能性中的作用和此类等位基因在特定人群中的频率,以此来研究疾病风险
  • 能让程序将精心设计的检测集中用于标记为具有有趣或可疑发现的特定样本,对样本进行分层以节省成本。
  • 激励参与,通过生成结果为参与者提供价值,扩展项目的样本量和探索能力。
可靠的实验分析方法和高通量工作流程

芯片支持唾液、血液和口腔拭子等样本类型的基因分型和CNV检出。其形式支持每周处理数千份样本,群体规模研究工作流程为3天。

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Frequently Purchased Together

规格

产品比较

Infinium Global Screening Array-24 Kit Infinium Multi-Ethnic Global-8 Kit Infinium Omni2.5-8 Kit
Description An economical next-generation genotyping array that enables population-scale genetics, translational research, variant screening studies, and precision medicine research by combining highly optimized multiethnic genome-wide content, curated clinical research variants, and QC markers. With content from a variety of resources, this multiethnic array allows researchers to detect both common and rare variants across the most commonly studied 5 superpopulations in order to impute variants in a vast number of subpopulations. 8-sample arrays with high throughput and optimized tag SNP content, including full support of copy number variation applications, designed to be highly customizable and maximally informative for studying diverse world populations.
Number of Markers Fixed markers: ~ 654,027
Custom marker add-on capacity: Up to 50,000
Fixed markers: 1,779,819
Custom marker add-on capacity: Up to 245,000
Fixed markers: ~2,381,000, Custom marker add-on capacity: None
Number of Samples 24 samples per array 8 samples per array 8 samples per array
Sample Throughput ~5760 samples/week max per iScan (throughput and scan times may vary based on laboratory and system configurations.) ~1728 samples/week max per iScan (throughput and scan times may vary based on laboratory and system configurations.) ~1728 samples/week per iScan (max throughput and scan time may vary based on lab and system configurations)
技术 微阵列芯片 微阵列芯片 微阵列芯片
核酸类型 DNA DNA DNA
物种类别 人类 人类 人类

方法特异的工作流程示例

 

Case Studies and Feature Articles

Scalable High-Throughput Array Enables Ethnic Chinese Genome Database Development
Scalable High-Throughput Array Enables Ethnic Chinese Genome Database Development

Fast Infinium array analysis and broad genome coverage support personal genetic testing services and database development.

Read Interivew
Bringing Meaning to Genetic Information
Bringing Meaning to Genetic Information

MyDNA recently began partnering with Illumina customers using the Global Screening Array and Asian Screening Array in their genetic test offerings.

Read Interview
A Genetic Data Matchmaking Service for Researchers
A Genetic Data Matchmaking Service for Researchers

Sano Genetics connects researchers with valuable information about rare disorders while protecting individual's privacy.

Read Interview
Genetic Testing Services Gain a Presence in India

The Global Screening Array and iScan System are helping Mapmygenome bring consumer genomics to a rapidly growing Indian population.

Read Article
Genetic Testing Services Gain a Presence in India
基因panel和芯片查找工具

芯片是一种很有价值的变异检测工具。借助基因panel和芯片查找工具,您可以用基因组位置或变异ID搜索人类芯片,或查找其他物种的芯片。

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基因panel和芯片查找工具

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