Order the NovaSeq X Series
Advanced chemistry, optics, and informatics combine to deliver exceptional speed and data quality, outstanding throughput and scalability.
This BeadChip array covers > 4.3 million whole-genome variants down to 1% minor allele frequency (MAF), plus novel functional exonic variants.
Sample throughput
Number of samples
Number of markers
The semi-custom Omni5Exome-4+ kits (catalog numbers WG-313-5014, WG-313-5015, WG-313-5016, and WG-313-5017) have been discontinued. Also, the prior non-custom kit versions (WG-313-5010, WG-313-5011, WG-313-5012, and WG-313-5013) have been replaced with the v1.3 catalog numbers shown in the add-to-cart area.
The HumanOmni5Exome-4 BeadChip Kit has been renamed to Infinium Omni5Exome-4 Kit. Kits with either name on the label contain the same quality reagents and follow the same workflow.
The Infinium Omni5Exome-4 BeadChip array delivers comprehensive coverage of the genome, providing functional exonic content for whole-genome genotyping and copy number variation (CNV) studies. The BeadChips include optimized tag single nucleotide polymorphisms (SNPs) targeting genetic variation down to 1% minor allele frequency (MAF).
Using the proven iScan array scanner and integrated analysis software, these BeadChips offer optimized tag SNPs, exonic content, and fully supported CNV analysis. Combined with convenient packaging and a streamlined PCR-free protocol, these kits provide a comprehensive DNA analysis solution.
Assay type | Infinium LCG Quad |
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Automation capability | Liquid handling robots, Automated array loader |
Description | A high-density array that provides coverage of common, intermediate, and rare SNPs using functional exonic content, for genome-wide genotyping and copy number variation studies. |
Input quantity | 400 ng DNA |
Instruments | iScan System |
Method | Exome array |
Nucleic acid type | DNA |
Number of markers | Fixed markers: 4,548,474, Custom marker add-on capacity: None |
Number of samples | 4 samples per array |
Sample throughput | ~544 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) |
Match your chosen kit size to the number of samples you run at a time. Each kit is processed as a single batch and is not designed to be divided across multiple experiments. If you are processing several low-throughput batches, order multiple small kits.
Microarrays and Array Techniques
Illumina microarrays offer high-quality data and exceptional genomic coverage to propel genomic studies of any size.
Large-scale genotyping with microarrays can identify variants associated with disease risk in large cohorts or populations.
Complex and Genetic Disease Research
Comprehensive array and next-generation sequencing solutions to accelerate research of various genetic complex diseases.
The HUNT Biobank and Lifandis AS provide access to biological samples and corresponding clinical data from more than 250,000 individuals in the Norwegian population using Illumina off-the-shelf and custom Infinium HumanExome BeadChips.
Infinium Omni5Exome-4 Kit | Infinium Exome-24 Kit | |
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Assay type | Infinium LCG Quad | Infinium HTS |
Automation capability | Liquid handling robots, Automated array loader | Liquid handling robots, Automated array loader |
Description | A high-density array that provides coverage of common, intermediate, and rare SNPs using functional exonic content, for genome-wide genotyping and copy number variation studies. | Study putative functional exonic variants that consist of >240,000 markers representing European, African, Chinese, and Hispanic individuals, and a range of common conditions, from type 2 diabetes to cancer, psychiatric disorders, and more. |
Input quantity | 400 ng DNA | 200 ng DNA |
Instruments | iScan System | iScan System |
Nucleic acid type | DNA | DNA |
Number of markers | Fixed markers: 4,548,474, Custom marker add-on capacity: None | 244,883 fixed markers. Custom marker add-on capacity: Up to 400,000 (with + kit versions). |
Number of samples | 4 samples per array | 24 samples per array |
Sample throughput | ~544 samples per week (estimate for 2 iScan Systems, 1 AutoLoader 2.x, 3 Infinium Automated Pipetting Systems, and a 5-day work week) | ~2304 samples per week (estimate for 1 iScan System, 1 AutoLoader 2.x, 2 Infinium Automated Pipetting Systems, and a 5-day work week) |
Specialized sample types | FFPE tissue | FFPE tissue |
Species category | Human | Human |
Variant class | Single nucleotide polymorphisms (SNPs), Germline variants, Structural variants, Insertions-deletions (indels), Copy number variants (CNVs) | Single nucleotide polymorphisms (SNPs), Germline variants, Structural variants, Insertions-deletions (indels), Copy number variants (CNVs) |
Infinium® Omni5Exome-4 v1.3 Kit (16 samples)
20005140
The Infinium Omni5Exome-4 v1.3 BeadChip can process 4 samples and analyze ~4.5M loci. Each package contains 4 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 16 DNA samples.
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Infinium® Omni5Exome-4 v1.3 Kit (48 samples)
20005141
The Infinium Omni5Exome-4 v1.3 BeadChip can process 4 samples and analyze ~4.5M loci. Each package contains 12 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 48 DNA samples.
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Infinium® Omni5Exome-4 v1.3 Kit (96 samples)
20005142
The Infinium Omni5Exome-4 v1.3 BeadChip can process 4 samples and analyze ~4.5M loci. Each package contains 24 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 96 DNA samples.
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Infinium® Omni5Exome-4 v1.3 Kit (384 samples)
20005143
The Infinium Omni5Exome-4 v1.3 BeadChip can process 4 samples and analyze ~4.5M loci. Each package contains 96 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling and detecting 384 DNA samples.
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