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Overview
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MGIEasy Exome Capture V5 Probe Set not only covers the regions of traditional exome probes, but also ensures the comprehensive capture of coding sequences related to various diseases by targeted design, e.g. reproductive, neonatal, cardiovascular and cerebrovascular, hereditary tumors/deafness, monogenic, medication safety, personal genome, immunodeficiency, mitochondrial defects etc. The primary targets with a design size of 69Mb include: CCDS, GENCODE, RefSeq, miRbase and MGI Clinical Database. As a universal exome capture probe set, it is compatible with both of MGI and otherngS platforms.
Features
• Probe regions 69Mb
The databases used for probe design include CCDS, GENCODE, RefSeq, miRBase and so on. It also ensures the comprehensive capture of coding sequences related to various diseases by targeted design, e.g. reproductive, neonatal, cardiovascular and cerebrovascular, hereditary tumors/deafness, monogenic, medication safety, personal genome, immunodeficiency, mitochondrial defects etc.
• More comprehensive gene coverage
455 genes can be 100% covered.
• Superior coverage and uniformity
When the mean sequencing depth is 100X, 96% of the regions can reach coverage of 20X.
• Stable and efficient capture rate
The capture rate is over >60% (by reads).Please contact us at for specific academic pricing.
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- Properties
- Applications
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Overview