A fully customizable microarray to interrogate virtually any target across any species to fit your unique study needs.
Sample throughput
Number of samples
Number of markers
The Infinium HTS iSelect Custom BeadChips provide access to virtually any marker in the genome to fit unique research needs.
Custom genotyping panels of 3072 to 700K markers per sample can be created in a 24-sample format. Interrogate virtually any target (eg, SNPs, CNVs, indels) to enable focused genotyping applications tailored to specific projects.
Increase efficiency and cost effectiveness of custom studies by combining existing marker sets with new, unique content with the Infinium iSelect+ option.
Process data directly in Illumina GenomeStudio software to provide streamlined genotype calling, analysis, and reporting.
| Assay type | Infinium HTS |
|---|---|
| Automation capability | Automated array loader, Liquid handling robot(s) |
| Description | The Infinium HTS iSelect Custom BeadChip enables researchers to design a fully customized high-throughput screening panel to interrogate virtually any marker in the genome for virtually any species to fit their research needs. |
| Input quantity | 200 ng |
| Instruments | iScan System |
| Method | Custom array |
| Nucleic acid type | DNA |
| Number of markers | 700K custom markers max |
| Number of samples | 24 samples per array |
| Sample throughput | 5760 samples per week max (with 2 iScan systems, 1 AutoLoader 2x, and 2 Tecan robots over an 8-hour day) |
| Specialized sample types | FFPE tissue |
| Species category | Drosophila, Any species, Shrimp, Mammalian, Tomato, Bovine, Mouse, Canine, Yeast, Rice, Zebrafish, Ovine, Hamster, Chicken, Porcine, Human, Rat, Equine, Plant, Virus, Maize, Nematode, Bacteria, Soybean |
| Technology | Microarray |
| Variant class | Single nucleotide polymorphisms (SNPs), Germline variants, 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.
Optimized reagent kit that provides increased cluster density and read length, improving sequencing quality scores compared to earlier versions.
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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