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当前位置: 首页 > 产品中心 > Biochip > Illumina/TruSight肿瘤170 Kit plus Watson for Genomics/20018622/1 Ea
商品详细Illumina/TruSight肿瘤170 Kit plus Watson for Genomics/20018622/1 Ea
Illumina/TruSight肿瘤170 Kit plus Watson for Genomics/20018622/1 Ea
Illumina/TruSight肿瘤170 Kit plus Watson for Genomics/20018622/1 Ea
商品编号: 20018622
品牌: Illumina
市场价: ¥0.00
美元价: 0.00
产地: 美国(厂家直采)
公司:
产品分类: 芯片
公司分类: Biochip
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

ProductHighlights:

TruSightTumor170,anext-generationsequencingassaydesignedtocover170genesassociatedwithcommonsolidtumors,isanenrichment-basedtargetedpanelthatsimultaneouslyanalyzesDNAandRNA,coveringawiderangeofgenesandvarianttypes.Thecomprehensivenatureprovideslaboratorieswithadeepviewintothegeneticsofcancer.

  • ComprehensiveCoverageofCancer-RelatedVariants
    Assessmentoffusions,splicevariants,insertions/deletionsandsingle-nucleotidevariants(SNVs),andamplificationsinoneassayusingDNAandRNAcreatesefficienciesinsampleusage,time,andcost.
  • AccurateResultsfromLow-QualitySamples1
    Variantdetectionwithaslittleas40ngDNAandRNAinput,andaslowas5%mutantallelefrequency,maximizestheresultsfrompreciousformalin-fixedparaffin-embedded(FFPE)samples.
  • Integrated,StreamlinedWorkflow
    DNAandRNAarepreparedinparallelwithanintegratedworkflowfollowingDNAshearing/CDNAsynthesis.

Specifications:

AssayTime~2days(LibraryPrep)
Hands-OnTime~10.5hours
InputQuantity40ngDNAand/orRNA
MethodTargetedRNASequencing,TargetedDNASequencing
VariantClassSingleNucleotidePolymorphisms(SNPs),GeneFusions,SomaticVariants,StructuralVariants,Insertions-Deletions(indels),CopyNumberVariants(CNVs)
SpecializedSampleTypesFFPE,LowInput
SystemCompatibilityNextSeq550,NextSeq500,HiSeq2500
TechnologySequencing
SpeciesCategoryHuman
CancerTypeSolidTumor

ScientificPosters:

AACR2017:TruSightTumor170andTumorMutationalBurden

ResultsofanalysisindicatethatTruSightTumor170,withcomprehensivecoverageofcancer-relatedgenes,showshighconcordancewithwholeexomesequencingforaccurateassessmentoftumormutationalburden.

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AACR2017:TruSightTumor170andSolidTumorProfilingAnalyticalPerformancewithFFPESamples

StandardextractionsfromFFPEembeddedsamplesprovidesufficientmaterial(40ng)in>95%ofsamplesthatwereextractedbyIllumina.ThisdatashowsthattheTruSightTumor170panelisarobustassaythatgeneratespassingsampleQCdatain>85%ofsampleswithvaryingquality,andin>95%ofsamplesthathavequalitymetricsthatfallwithintherecommendationsforthekit.

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AACR2017:TruSightTumor170forSmallNucleotideVariationsandGeneAmplificationsinFFPEDNASamples

TruSightTumor170canachievehighsensitivityandspecificityforthedetectionofsomaticvariants(smallvariantsandCNVs)fromDNAextractedfromFFPEtissues.

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AACR2017:TruSightTumor170forFusionsandSpliceVariantsinFFPERNATumorSamples

ThroughexamininglimitofdetectioninthecontextofRNAexpression,thisstudyshowsthatTruSightTumor170provideshighsensitivityandspecificityinRNAvariantcallingdownto5copiesoftranscriptperngofinput.

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品牌介绍
基因组服务Illumina提供了多样化的服务组合,以支持广泛的基因组应用。无论您是进行基于人群的大规模基因分析研究,进行癌症研究还是推进育种计划,Illumina和我们的合作伙伴都能为您提供所需的解决方案。借助久经考验的Illumina NGS和阵列技术以及科学专家网络,客户越来越有能力加快发现机会。Illumina服务网络提供了一个从样品到数据的解决方案,可以保证交付高质量的数据,从而帮助您以前所未有的速度和效率找到答案。Illumina还提供许多其他服务,包括核心实验室计划,服务合作伙伴关系,分析和数据管理解决方案以及财务解决方案。