A powerful, cost-effective genotyping microarray for large-scale genetic studies and pharmacogenomics in East Asian populations.
Sample throughput
Number of samples
Number of markers
The Infinium Asian Screening Array Kit contains 24-sample BeadChips plus reagents for population genetic studies in East and Southeast Asian populations.
This microarray was designed in collaboration with leading institutions. Content includes a genome-wide backbone using clinical research variants, QC markers, a discovery panel, and custom add-on content.
This microarray builds on the commercial success of the Infinium Global Screening Array. > 20M samples of Illumina Infinium arrays have been ordered by a global community of users.
Genotyping and CNV calling are supported for multiple sample types (eg, saliva, blood, buccal swabs, and FFPE samples). The high-throughput workflow maximizes sample processing while minimizing costs, instrumentation, lab space, and hands-on time.
Predesigned booster content is available as an optional add-on.
| Assay type | Infinium HTS |
|---|---|
| Automation capability | Automated array loader, Liquid handling robot(s) |
| Description | Advanced genotyping array that provides a high-value, scalable, and cost-effective solution for population-scale genetic studies, variant screening, and precision medicine research in East and Southeast Asian populations. |
| Input quantity | 200 ng gDNA |
| Instruments | iScan System |
| Method | High-throughput genotyping array, Genome-wide genotyping array |
| Nucleic acid type | DNA |
| Number of markers | Fixed markers: ~ 660,000, Custom marker add-on capacity up to 50,000 |
| Number of samples | 24 samples per array |
| Sample throughput | ~2304 samples per week (estimate assumes 1 iScan System, 1 AutoLoader, 2 Tecan robots, and a 5-day work week) |
| Specialized sample types | Blood, FFPE tissue |
| Species category | Human |
| Technology | Microarray |
| Variant class | Single nucleotide polymorphisms (SNPs), Structural variants, Insertions-deletions (indels), Copy number variants (CNVs) |
Advanced chemistry, optics, and informatics combine to deliver exceptional sequencing speed and data quality, outstanding throughput, and scalability.
Reagent kits that provide increased cluster density and read length for the MiSeq System, improving sequencing quality scores compared to v1 kits.
Enable CGP with a large pan-cancer panel covering all major variant classes plus gene signatures (TMB, MSI, and HRD) from FFPE tissue.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
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