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NGS reagent kit AmpliSeq™20019109
for DNA sequencingfor mutation detectionfor cancers

NGS reagent kit
NGS reagent kit
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Characteristics

Applications
NGS, for DNA sequencing, for mutation detection, for cancers, for PCR, FFPE tissues, blood sample, for nucleic acids
Tested parameter
for genes

Description

Product Highlights The AmpliSeq for Illumina Comprehensive Panel v3 offers coverage of key cancer genes, including kinase domains and genes involved in DNA repair. Relevant Gene Content Target 161 unique cancer-associated genes Fast, Streamlined Workflow Prepare sequencing-ready libraries in a single day from as little as 1 ng of high quality or 10 ng of formalin-fixed, paraffin-embedded (FFPE) input samples Accurate Data Detect somatic mutations down to 5% frequency using local or cloud-based analysis The Comprehensive Panel v3 is part of an integrated workflow that includes AmpliSeq for Illumina polymerase chain reaction (PCR)-based library preparation, Illumina sequencing by synthesis (SBS) next-generation sequencing (NGS) technology, and automated analysis. The panel content spans hotspot regions, full-length genes, copy number genes, and inter- and intragenic gene fusions. This ready-to-use panel saves you the time and effort of identifying targets, designing primers, and optimizing panels.

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