Infinium Global Screening Array-24 Kit

Genotyping array providing a scalable, cost-effective solution for population genetics, pharmacogenomics studies, and precision medicine research.

5760

Sample throughput

24 sample…

Number of samples

654,027 f…

Number of markers

See full details in the specifications table

Overview

The Infinium Global Screening Array-24 BeadChip is an advanced, scalable, and cost-effective solution for population-scale genetic studies.

Key features

  • Multiethnic genome-wide content selected for high imputation accuracy of > 1% across all 26 1000 Genomes Project Populations

  • High-throughput processing of hundreds to thousands of samples per week with a 3-day workflow for population-scale studies

  • Clinical research applications include disease risk profiling studies, pharmacogenomics research, wellness characterization, and complex disease discovery

Optimized global content

Clinical research content in v3.0 includes variants with established disease associations, relevant pharmacogenomics markers, and curated exonic content derived from ClinVar, NHGRI, PharmGKB, and ExAC databases.

Widely adopted

Over 15 million samples of the Global Screening Array have been ordered by researchers, healthcare networks, consumer genomics companies, and genomic service providers.

Broad applications

Precision medicine research initiatives around the world use the Global Screening Array to study disease risk, stratify samples, and incentivize participation across a large variety of clinical applications.

Specifications

Required products

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FAQs

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NovaSeq X Series ordering

Advanced chemistry, optics, and informatics combine to deliver exceptional sequencing speed and data quality, outstanding throughput, and scalability.

MiSeq Reagent Kit v3

Optimized reagent kit that provides increased cluster density and read length, improving sequencing quality scores compared to earlier versions.

TruSight Oncology 500

Enable CGP with a large pan-cancer panel covering all major variant classes plus gene signatures (TMB, MSI, and HRD) from FFPE tissue.

Illumina DNA Prep

A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.

References
  1. The 1000 Genomes Project. http://www.1000genomes.org. Accessed May 20, 2020.
  2. PharmGKB, The Pharmacogenomics Knowledgebase. www.pharmgkb.org. Accessed May 20, 2020.

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