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DNA sequencing reagent kit AmpliSeq™ 20019160
NGSfor mutation detectionfor cancers

DNA sequencing reagent kit
DNA sequencing reagent kit
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Characteristics

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

Description

Product Highlights The AmpliSeq for Illumina Comprehensive Cancer Panel provides a targeted resequencing solution for analyzing somatic mutations across 409 genes with known associations to cancer. Key features include: Relevant Gene Content Target all-exon coverage of 409 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 below 5% frequency using local or cloud analysis The Comprehensive Cancer Panel 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. This panel detects variants within multiple cancer types, including lung, colon, breast, ovarian, melanoma, and prostate malignancies. The ready-to-use panel saves you the time and effort of identifying targets, designing primers, and optimizing panels.

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