Total RNA-seq--stranded whole transcriptome sequencing
NOTE: We are updating the names and formats of several of our NGS RNA-seq kits. Details of the changes are provided on the relevant product pages for these kits. See a complete list of kits with new names and the existing kits they will replace here.
RNA-seq can be used to understand the complex biology of gene regulation and assist in understanding gene expression from a wide range of different sample types. With our stranded RNA-seq kits, you can access valuable stranded gene expression data on coding and noncoding transcripts from a wide range of samples and inputs. SMART technology has been incorporated into several of our kits to perform RNA-seq using a random priming approach. This approach can help in developing a better understanding of biology in a number of different applications, including:
- Interrogating sequences that are not polyadenylated, such as noncoding regulatory RNAs or degraded RNAs from FFPE or plasma
- Providing strand information for more accurate measurement of RNAs from overlapping genes
- Giving information on splice variants from genes of varying length
Cancer transcriptome analysis with total RNA-seq
Learn how our products can help you uncover biomarkers from a broad range of sample types, including FFPE RNA, cell-free RNA, and extracellular vesicles.
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