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HumanExome BeadChip

 

The HumanExome BeadChip provides coverage of functional exonic variants. The >250,000 markers on this BeadChip were selected from >12,000 whole exome and whole genome sequences, and represent SNPs in RefSeq genes, nonsynonymous SNPs and SNPs in coding regions (including UTR’s).

 

The array was consortium designed with the goal of enabling a bridge between GWAS genotyping for common variants and exome sequencing for relatively rare variants.

 

• Detailed Information on Array Design
• Specific SNP Information

 

The content of HumanExome BeadChip can be customized with the ability to add additional SNPs. In addition, the core content of the HumanExome array can be added to all GWAS arrays.

 

• Additional Information on the HumanExome BeadChip

 

 

Array	SNPs per Sample	Samples per Array	Comments
Illumina HumanExome	>240,000	12	Coverage of putative functional exonic variants selected from 12,000 Exome and whole genome sequences

 

 

 

 

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Illumina BeadChips

 

See our Services page for a full description of what is included for all study types

 

 

See our Sample Requirements page for detailed specifications for each product