簡要描述:Sequencing Kits/ Microarray Kits/Informatics ProductsIllumina/TruSight Cancer MiniSeq Kit/20005612/1 Ea
詳細介紹
品牌 | illumina/美國因美納 | 貨號 | 20005612 |
---|---|---|---|
規(guī)格 | 1 kit | 供貨周期 | 兩周 |
主要用途 | 小型全基因組測序 組合試劑 試劑盒 | 應用領域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
"Illumina/TruSight Cancer MiniSeq Kit/20005612/1 Ea
" 20005612 Illumina 產(chǎn)品編號: 20005612美 元 價: $0.00會 員 價: 待定品 牌: Illumina產(chǎn) 地: 美國公 司: Illumina, Inc.產(chǎn)品分類: 其它>其它試劑>芯片公司分類: Clinical Research Products "Product Highlights:
Targeting genes previously linked to a predisposition towards cancer.
Developed in collaboration with Professor Nazneen Rahman and team at the Institute of Cancer Research (ICR), London
Targets 94 genes and 284 SNPs associated with a predisposition towards cancer
TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources.
The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatIBLe with TruSight Rapid Capture.
TruSight Cancer Sample Datasets
6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30.
Browse the data in BaseSpace Sequence Hub:
View Run
View Project
* Note that access to this data requires a BaseSpace Sequence Hub login.
Register for BaseSpace Sequence Hub
Specifications:
Assay Time 1.5 days
Input Quantity 50 ng
System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500
Specialized Sample Types Low Input
Technology Sequencing
Species Category Human
Variant Class Germline Variants
Cancer Type Pan-Cancer
Method Targeted DNA Sequencing
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