RNA-Seq Services

Introduction

mRNA-Seq : targeting poly(A) RNA provides a sensitive option lowly expressed coding transcripts
Whole Transcriptome : RNA sample are enriched for both mRNA and non-coding RNAs to provide a comprehensive view of the transcriptome
Low Input Whole Transcriptome : RNA-Seq for samples with limited quantities of RNA, including small tissue biopsies and FACS sorted cells
Small RNA : targets small regulatory RNAs such as miRNA for profiling and discovery.

Summary

RNA sequencing (RNA-Seq) is powerful method for qualitative and quantitative analysis of the transcriptome of any organism. RNA-Seq is used for differential gene expression, detection of alternate splicing and characterisation of novel transcripts.

CD Genomics has already updated its technology platforms to mainstream NGS, long-read sequencing, and microarray instruments. We continue to strive to offer the same reliable services to pharmaceutical and biotechnology companies, as well as academia and government agencies, for all your sequencing or array needs. If you are interested, please contact us directly for assistance.