簡(jiǎn)要描述:Illumina公司基因芯片、二代測(cè)序NGS測(cè)序儀及相關(guān)測(cè)序試劑盒等產(chǎn)品Illumina/TruSight Tumor 15 (Library Prep Only)/OP-101-1002/1 Ea
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品牌 | illumina/美國(guó)因美納 | 貨號(hào) | OP-101-1002 |
---|---|---|---|
規(guī)格 | 1 kit | 供貨周期 | 兩周 |
主要用途 | 小型全基因組測(cè)序 組合試劑 試劑盒 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
"Illumina/TruSight Tumor 15 (Library Prep Only)/OP-101-1002/1 Ea
" OP-101-1002 Illumina 產(chǎn)品編號(hào): OP-101-1002美 元 價(jià): $0.00會(huì) 員 價(jià): 待定品 牌: Illumina產(chǎn) 地: 美國(guó)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:
TruSight Tumor 15 uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 15 genes that are commonly mutated in solid tumors. It accurately detects low-frequency variants from 20 ng of starting DNA and is optimized for formalin-fixed, paraffin-embedded (FFPE) tumor tissue.
View the Gene List
Featuring a rapid workflow that can be easily integrated into lab procedures, this panel offers a single assay for accurate, economical, and rapid analysis of solid tumors.
This TruSight Tumor panel offers:
Comprehensive workflow: Assess 15 genes with one simple workflow instead of single, iterative gene testing with polymerase chain reaction (PCR)
Efficient: Rapid turnaround with only 3.5 hours of hands-on time, going from DNA to data in approximately 36 hours
Relevant gene content for solid tumors: Somatic variants selected from relevant industry guidelines1,2, key opinion leaders3,4, and pharmaceutical research
Sensitive variant detection from low DNA input: Accurate somatic variant detection of 5% allele frequency using 20 ng DNA from FFPE tissue samples
TruSight Tumor 15 Sample Datasets
3 human reference samples and 5 FFPE-exacted DNA samples from lung, colon, melanoma, and breast tumors were prepared using TruSight Tumor 15. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 150 bp read length configuration with dual indexing. The total yield was 7.6 Gb with 94.9% of bases at or above Q30.
Browse the data in BaseSpace Sequence Hub:
View Run
View Project
Access to this data requires a BaseSpace Sequence Hub login.
Register for BaseSpace Sequence Hub
Specifications:
Assay Time 7 hours
Hands-On Time 3.5 hours
Input Quantity 20 ng
System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq
Specialized Sample Types FFPE,Low Input
Technology Sequencing
Variant Class Somatic Variants,Insertions-Deletions (indels)
Species Category Human
Cancer Type Solid Tumor
Method Amplicon Sequencing,Targeted DNA Sequencing
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