RNA sequencing uses next-generation sequencing (NGS) to uncover the presence and quantity of RNA for gene expression profiling across the transcriptome. Diagenode utilizes the unique capture and amplification by tailing and switching (CATS) methodology for generating RNAseq libraries which is optimal for low or degraded inputs including those from liquid biopsies, FFPE, exosomes, serum, or plasma.
Ideal for low input samples including patient samples
Proven to detect more transcripts than any other commercial method
Full range of RNA-seq services and RNA-seq analysis including the quantification of known transcripts:
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