Epigenomics Profiling Services

RNA-seq Profiling Services

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:

Small non-coding RNA including miRNA

Post-transcriptional regulation of gene expression
Novel transcripts and differentially-expressed small RNAs
miRNAs involved in regulation of onco- and tumor-suppressor gene expression
Differential miRNA expression

mRNA analysis

Protein-coding RNA with specific poly A selection
Cancer-related mRNA signatures
Aberrant mRNA translation in cancer pathogenesis
Gene expression profiling and identification of differentially expressed genes (DEG)
Epigenetic mechanism of gene expression (transcriptome plus H3K36me3 and H3K4me3 marks)
Functional annotation of coding genes

Long non-coding RNA and whole transcriptome

Explore the effects of transcription factor binding through ChIP-seq analysis of a multitude of TFs including:

Analysis of whole transcriptome and RNAs larger than 200nt with optional rRNA depletion
Non-protein coding RNAs involved in chromatin remodeling & transcriptional/post-transcriptional regulation

Products

RNA-seq services

Diagenode uses proprietary ligation-free CATS-based technology for RNA-seq library preparation Read more about CATS Ideal for low input samples includin...

CATS White paper

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