AmpliSeq:AmpliSeq for Illumina Custom DNA Panel

AmpliSeq for Illumina Custom DNA Panel

AmpliSeq for Illumina Custom DNA Panel

AmpliSeqforIlluminaCustomDNAPanel.Targetedcustomresearchpanelsoptimizedforsequencingspecifictargetsorgenomiccontentofinterest.ReadMore.。其他文章還包含有:「AmpliSeqforIlluminaCustomDNAPanel...」、「AmpliSeqforIlluminaMyeloidPanel」、「AmpliSeqforIlluminaOn」、「AmpliSeqforIlluminaReady」、「AmpliSeqforIlluminaSequencingSolution」、「IonAmpliSeqDesigner」、「IonAmpliSeqNGSPanels」

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AmpliSeq for Illumina Custom DNA Panel ...
AmpliSeq for Illumina Custom DNA Panel ...

http://www.gtbiotech.com.tw

【illumina】AmpliSeq for illumina Custom Panels · 客製化試劑套組,使用DesignStudio線上平台免費進行設計 · 只需1~100 ng DNA/RNA樣品 · 適用於FFPE、血液檢體 · 可搭配 ...

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AmpliSeq for Illumina Myeloid Panel
AmpliSeq for Illumina Myeloid Panel

https://www.illumina.com

AmpliSeq for Illumina Myeloid Panel. Targeted panel to investigate 40 DNA genes, 29 RNA fusion driver genes, and 5 gene expression levels associated with ...

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AmpliSeq for Illumina On
AmpliSeq for Illumina On

https://www.illumina.com

AmpliSeq for Illumina On Demand panels provide a choice of > 5000 pretested genes with known content relevant for inherited disease research, ...

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AmpliSeq for Illumina Ready
AmpliSeq for Illumina Ready

https://www.illumina.com

Ready-to-Use AmpliSeq panels provide a fast and cost-effective way to start your research instead of spending time designing amplicons and target selections ...

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AmpliSeq for Illumina Sequencing Solution
AmpliSeq for Illumina Sequencing Solution

https://www.illumina.com

AmpliSeq chemistry allows researchers to analyze hundreds of genes simultaneously with ultra-high multiplexed PCR with 12 to more than 24,000 amplicons in a ...

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Ion AmpliSeq Designer
Ion AmpliSeq Designer

https://www.ampliseq.com

A free design tool that helps you obtain custom assay designs based on PCR target selection.

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Ion AmpliSeq NGS Panels
Ion AmpliSeq NGS Panels

https://www.thermofisher.com

Ion AmpliSeq technology is globally recognized as the gold-standard, amplicon-based enrichment method for targeted next-generation sequencing (NGS).