Transcriptomic analysis

With the Illumina sequencing technology, ServiceXS is able to offer various services, including transcriptome sequencing, gene expression profiling and DeepCAGE.

Gene Expression profiling by sequencing is a truly unbiased approach for discovery and quantification, in contrast to microarray profiling. Different approaches to transcriptome profiling offers a genome-wide overview of gene expression, cSNPs, novel transcripts, novel isoforms, alternative splice sites, allele-specific expression, miRNAs, rare transcripts, and transcription start sites.

Transcriptome analysis is ideal for the characterization of splice variants, coding SNPs, and relative expression levels of transcripts in one experiment, profiling rare transcripts, and RNA discovery. With mRNA Seq, you can identify full-length polyA transcript isoforms.

Applications:

• (de novo) Whole Transcriptome Sequencing: Find uncharacterized transcripts, coding disease associated SNPs, update genome annotations with accurate localization of UTRs and exons or simply measure gene expression levels.
• small RNA analysis: Discover rare small RNA/miRNAs without previous sequence information in any species: an unbiased discovery and quantification method for microRNA analysis.
• DeepCAGE: Genome wide analysis of 5'-ends of mRNA transcripts.

For more information on these services, please contact us to discuss your future project, or go to our inforequest NGS form.