Services
RNA sequencing (RNAseq) provides unbiased, specific, and sensitive quantification of coding and non-coding RNA transcripts. Also, the alterations such as splice variants, gene fusions, mutations, and RNA editing events.
RNAseq is the preferred method for numerous clinical applications including:
CellCarta leverages the power of next-generation sequencing (NGS) by using the NovaSeq X Plus , NovaSeq 6000, and NextSeq 550Dx platforms.
Our offering spans from RNA extraction, library preparation, and sequencing, to data analysis and reporting.
To further support your findings, we provide orthogonal result validation using quantitative PCR and digital PCR.
Depletion of unwanted RNA molecules from the total RNA investigated is also offered.
For targeted gene expression studies for specific mRNA, microRNA, or lncRNA genes or gene panels, off-the-shelf assays for almost all genes are available here at CellCarta.
We also offer numerous gene expression panels (mRNA, microRNA, and lncRNA) for a broad range of pathways and disease states.
For genes where no off-the-shelf assay is available, assays can be developed with custom primers.
| Application | Library kit used |
|---|---|
| RNA capture | TruSeq® Stranded mRNA Library Prep (Illumina®) |
| small RNA | NEBNext® Multiplex Small RNA Library Prep Kit for Illumina® |
| RNA capture | TruSeq® RNA exome library (Illumina®) RNA Prep with Enrichment, (L) Tagmentation kit (Illumina®) |
| High-throughput RNAseq | QuantSeq 3’ mRNA-Seq Library Prep Kit FWD for Illumina® |
| Total RNA | SMARTer® Stranded Total RNA-Seq Kit (Takara Bio) |
| Custom Capture | Design of custom capture probes |
Based on your sequencing needs, our team can develop a customized sequencing workflow which can be applied to various sample types, like-
Get insights on the mode of action underlying induced cellular phenotypes, reveal potential compound-induced toxicities or off-target effects, and compound similarities with our high throughput molecular cellular phenotyping service.
To bridge the demand between expression data of genes for a few samples by classic RNA sequencing and for thousands of samples at low cost by qPCR, our team developed a high-throughput shallow 3’ RNA sequencing method using crude cell lysates.
The workflow can process up to 384 cell lysates without the need for RNA extraction.
Data is shared through Savanna, our proprietary data visualization app to help you visualize and compare data points.
Contact us to learn more about our high throughput RNA Sequencing Services for pre-clinical compound screening
RNA profiling has emerged as a powerful tool to investigate the biomarker potential of human biofluids.
Our team published an RNA sequencing method using a dedicated RNA library kit to properly quantify extracellular RNA content and provide the complete transcriptome of a wide range of biofluids.
Learn more about performance assessment of total RNA sequencing of human biofluids and more.
Our expertise in RNA sequencing is showcased in numerous publications: