Solution reagent kit AmpliSeq™ Library PLUS

sample preparationfor PCRblood sample

The AmpliSeq for Illumina Custom RNA Fusion Panel enables detection of fusion genes and gene expression profiling in 12 to 1200 gene targets in a single assay. Targeted panels can be designed from a menu of over 1000 well-annotated fusion genes and > 20,000 human RefSeq genes using DesignStudio—a web-based assay design software tool. Key features include: Fast Gene Fusion Detection Prepare libraries in 6 hours with < 1.5 hours hands-on time. Results are available in < 2 days. Low-Quality, Low-Quantity Sample Input Obtain high-quality data even when starting with minimal input from formalin-fixed, paraffin-embedded (FFPE) tissues. RNA-to-Analysis Solution Take advantage of a comprehensive workflow that spans library preparation, sequencing, and analysis. An AmpliSeq for Illumina Custom RNA Panel is part of an integrated workflow that includes AmpliSeq for Illumina polymerase chain reaction (PCR)-based library preparation, Illumina sequencing by synthesis (SBS) chemistry and next-generation sequencing (NGS) technology, and automated analysis. Specifications Automation capability - Liquid handling robots Cancer type - Hematologic, Solid tumor Strand specificity - Non-stranded Technology - Sequencing Variant class - Gene fusions, Transcript variants