Order the NovaSeq X Series
Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.
This 4-sample BeadChip array, optimized for genome-wide genotyping and CNV studies, covers > 4.3 million variants.
Sample throughput
Number of samples
Number of markers
The semi-custom Omni5-4+ kits (catalog numbers WG-313-5005, WG-313-5006, WG-313-5007, and WG-313-5008) have been discontinued. Also, the prior non-custom kit versions (WG-313-5001, WG-313-5002, WG-313-5003, and WG-313-5004) have been replaced with the v1.2 catalog numbers shown in the add-to-cart area.
The Infinium Omni5-4 BeadChip array (formerly known as the HumanOmni5-4 Beadchip Kit) delivers delivers comprehensive coverage of the genome, leveraging powerful tagSNPs selected from the International HapMap and 1000 Genomes Projects that target genetic variation down to 1% minor allele frequency (MAF).
Using the proven iScan System, this four-sample BeadChip offers high-throughput sample processing, with optimized content for whole-genome genotyping and copy number variation (CNV) studies.
Automation capability | Liquid handling robots, Automated array loader |
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Description | A high-density array that provides exceptional coverage of common, intermediate, and rare SNPs while leveraging powerful tag SNPs and offering optimized content for whole-genome genotyping and copy number variation studies. |
Input quantity | 400 ng DNA |
Instruments | iScan System |
Method | Genome-wide genotyping array |
Nucleic acid type | DNA |
Number of markers | Fixed markers: 4,284,426, Custom marker add-on capacity: None |
Number of samples | 4 samples per array |
Sample throughput | >460 samples per week (estimate for 2 iScan Systems, 1 AutoLoader 2.x, 3 Infinium Automated Pipetting Systems, and a 5-day work week) |
Specialized sample types | FFPE tissue |
Species category | Human |
Technology | Microarray |
Variant class | Single nucleotide polymorphisms (SNPs), Germline variants, Structural variants, Insertions-deletions (indels), Copy number variants (CNVs) |
Large-scale genotyping with microarrays can identify variants associated with disease risk in large cohorts or populations.
With targeted resequencing, a subset of genes or a genomic region is isolated and sequenced, which can conserve lab resources.
Microarray data analysis and experimental design
Find microarray data analysis tools and tips to help you to visualize and analyze microarray data and facilitate data analysis for large experiments.
Infinium Omni5-4 Kit | Infinium Global Diversity Array-8 Kit | |
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Automation capability | Liquid handling robots, Automated array loader | Liquid handling robots, Automated array loader |
Description | A high-density array that provides exceptional coverage of common, intermediate, and rare SNPs while leveraging powerful tag SNPs and offering optimized content for whole-genome genotyping and copy number variation studies. | 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. |
Input quantity | 400 ng DNA | 200 ng DNA |
Instruments | iScan System | iScan System |
Method | Genome-wide genotyping array | Genome-wide genotyping array |
Nucleic acid type | DNA | DNA |
Number of markers | Fixed markers: 4,284,426, Custom marker add-on capacity: None | 1,825,277 fixed markers. Custom marker add-on capacity: Up to 175K. |
Number of samples | 4 samples per array | 8 samples per array |
Sample throughput | >460 samples per week (estimate for 2 iScan Systems, 1 AutoLoader 2.x, 3 Infinium Automated Pipetting Systems, and a 5-day work week) | ~1728 samples per week |
Specialized sample types | FFPE tissue | Blood, FFPE tissue, Buccal swabs, Saliva |
Species category | Human | Human |
Technology | Microarray | Microarray |
Variant class | Single nucleotide polymorphisms (SNPs), Germline variants, Structural variants, Insertions-deletions (indels), Copy number variants (CNVs) | Single nucleotide polymorphisms (SNPs), Loss of heterozygosity (LOH), Chromosomal abnormalities, Structural variants, Copy number variants (CNVs) |
Infinium® Omni5-4 v1.2 Kit (16 samples)
20005150
The Infinium Omni5-4 v1.2 BeadChip can process 4 samples and analyze ~ 4.3M loci. Each package contains 4 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 16 DNA samples.
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Infinium® Omni5-4 v1.2 Kit (48 samples)
20005151
The Infinium Omni5-4 v1.2 BeadChip can process 4 samples and analyze ~ 4.3M loci. Each package contains 12 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 48 DNA samples.
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Infinium® Omni5-4 v1.2 Kit (96 samples)
20005152
The Infinium Omni5-4 v1.2 BeadChip can process 4 samples and analyze ~ 4.3M loci. Each package contains 24 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 96 DNA samples.
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Infinium® Omni5-4 v1.2 Kit (384 samples)
20005153
The Infinium Omni5-4 v1.2 BeadChip can process 4 samples and analyze ~ 4.3M loci. Each package contains 96 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 384 DNA samples.
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