Targeted RNA-Seq allows the analysis of transcripts of interest including those resulting from alternative splicing or gene fusion events and uses fewer sequencing reads than would be required in the context of global analysis
SMARTer Target RNA Capture for Illumina
Documents and resources
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NGS Library preparation tool for sequencing of small RNAs with high sensitivity and minimal bias
The best-in-class tools for rapid and accurate RNA-seq from the entire transcriptome
High sensitive approach to TCR and BCR sequencing
Prepare libraries in as little as one hour by fully automated NGS Library Prep System