Transcriptome analysis enables characterisation of coding and non-coding RNAs present in cells or tissues as well as comparison of gene expression or RNA isoform levels between different conditions. With deep sequencing it is also possible to characterise de novo transcriptomes and coding variants. According to your needs, we offer either full or partial service for transcriptome analysis by using next-generation sequencing based solutions:

• total RNA
• polyA+ RNA, mRNA
• small RNA, miRNA
• targeted RNA panel

The service includes QC analysis of nucleic acids, library preparation, next-generation sequencing and QC analysis of the raw data. The cost of the service depends e.g. on application, number of samples and required sequencing depth. For further information please fill in our NGS Project Request Form or send an email to ffgc@bioscience.fi, and we will contact you as soon as possible.