The Infinium Global Diversity Array with Carrier Screening Content-8 v2.0 Kit offers superb coverage of high-value clinical research variants.
Pan-ethnic, expanded disorder coverage in one assay
The Infinium Global Diversity Array with Carrier Screening Content-8 v2.0 Kit features updated content, including screening coverage of 602 specific genes utilizing the 45K ACMG-recommended variants on a 1.8M genome-wide backbone to provide comprehensive coverage across high-value regions. A single assay can detect sequence and structural variation, significantly reducing hands-on time. Built on proven Infinium LCG technology, this automation-compatible assay can run up to 1728 samples per week using a single iScan System.
Access to Igentify Analyze software
The Infinium Global Diversity Array with Carrier Screening Content-8 v2.0 Kit is performs effectively with Igentify Analyze software for simplified data analysis. This easy-to-use software enables researchers to build a custom panel, confirm findings, and analyze results from raw microarray data. The Igentify Analyze software uses specialized algorithms to identify historically difficult-to-call variants.
| Infinium Global Diversity Array with Carrier Screening Content-8 v2.0 Kit | Infinium Global Diversity Array-8 Kit | Infinium Global Screening Array-24 Kit | |
|---|---|---|---|
| Assay Type | Infinium LCG | Infinium LCG | Infinium HTS |
| Automation Capability | Automated Array Loader, Liquid Handling Robots | Automated Array Loader, Liquid Handling Robots | Automated Array Loader, Liquid Handling Robots |
| Description | The Infinium Global Diversity Array with Carrier Screening Content-8 BeadChip expands carrier screening studies and features over 45K high-impact markers on the Global Diversity Array backbone. The Igentify Analyze software simplifies analysis, enabling high detection rates for key disorders. | The 8-sample Infinium Diversity Array provides targeted coverage of more than 4800 key genes across the genome. Approximately 1.8M markers are included on the BeadChip for high exonic coverage in regions of disease relevance, providing highly accurate copy number variation calls, and an average resolution of 1.5Mb. | 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. |
| Method | Genome-Wide Genotyping Array | Genome-Wide Genotyping Array | Genome-Wide Genotyping Array, High-Throughput Genotyping Array |
| Nucleic Acid Type | DNA | DNA | DNA |
| Number of Samples | 8 samples per array | 24 samples per array | |
| Specialized Sample Types | Blood | Blood, Buccal Swabs, FFPE Tissue, Saliva | Blood, Buccal Swabs, FFPE Tissue, Saliva |
| Species Category | Human | Human | Human |
| System Compatibility | iScan | iScan | iScan |
| Variant Class | Copy Number Variants (CNVs), Single Nucleotide Polymorphisms (SNPs), Structural Variants | Chromosomal Abnormalities, Copy Number Variants (CNVs), Loss of Heterozygosity (LOH), Single Nucleotide Polymorphisms (SNPs) |
Comprehensive, pan-ethnic microarrays capture clinically significant variants at the population level with high accuracy.
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