Custom OneSeq
客製化 OneSeq
Comprehensive, all-in-one detection of genome-wide CNVs, copy-neutral LOH (cnLOH), SNPs, and indels in one target enrichment capture.
Study both CNVs and mutations for your constitutional studies using one assay. OneSeq’s CNV backbone targets a functional copy number resolution of 300 kb in the genome-wide backbone, with an even higher resolution of 25-50 kb targeted in disease associated regions as defined by ClinGen. The targeting of genomic regions with high minor allele frequency SNPs allows for detection of copy neutral LOH at 5 Mb resolution.
產品資訊
- For copy number determination, experimental DNA samples are run side-by-side with a human reference DNA sample.
- Providing you the flexibility you need, OneSeq’s custom solution allows you to add your targeted regions of interest to the CNV backbone.
產品列表
| 貨號 | 產品 | 數量 | |
|---|---|---|---|
| 5190-8705 | OneSeq + Custom (1-499kb XT) | 16 rxns | |
| 5190-8887 | OneSeq + Custom (1-499kb XT) | 96 rxns | |
| 5190-8888 | OneSeq + Custom (1-499kb XT) | 96 rxns Auto | |
| 5190-8889 | OneSeq + Custom (0.5-2.9Mb XT) | 16 rxns | |
| 5190-8890 | OneSeq + Custom (0.5-2.9Mb XT) | 96 rxns | |
| 5190-8891 | OneSeq + Custom (0.5-2.9Mb XT) | 96 rxns Auto | |
| 5190-8892 | OneSeq + Custom (3-5.9Mb XT) | 16 rxns | |
| 5190-8893 | OneSeq + Custom (3-5.9Mb XT) | 96 rxns | |
| 5190-8894 | OneSeq + Custom (3-5.9Mb XT) | 96 rxns Auto | |
| 5190-8895 | OneSeq + Custom (6-11.9Mb XT) | 16 rxns | |
| 5190-8896 | OneSeq + Custom (6-11.9Mb XT) | 96 rxns | |
| 5190-8897 | OneSeq + Custom (6-11.9Mb XT) | 96 rxns Auto |
OneSeq Custom
- CNV Backbone (comprised of 300kb functional copy number resolution genome-wide, with higher resolution of 25-50kb in disease-associated ClinGen regions, and cnLOH as small as 5Mb)
- Add up to 12Mb of your gene targets via SureDesign
- For larger designs, please contact your local Agilent representative for more information
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