RNA-seq is a revolutionary technique that examines the total cellular content of RNAs, the transcriptome, using deep-sequencing technologies. Obtaining data about the transcriptome allows to connect the information on a genome with its functional protein expression. It provides great insights into cell development mechanisms and disease-associated modifications.
Our Epigenomics Profiling Services helps you to complete your transcriptomic profiling analysis using next-generation sequencing (NGS). Our experienced scientists will help you designing your RNA-seq experiments based on the ultimate goal of your transcriptomic profiling analysis, carefully take your samples in, generate meaningful RNA-seq libraries, and deliver high quality data. Our bioinformatic experts will closely work with you to provide standard and customized analysis with comprehensive publication-ready figures.
High-Throughput 3’mRNA-seq Service
High-throughput 3’mRNA-seq is an attractive solution to perform comparative gene expression analysis on a large number of samples. It utilizes the prop...
mRNA-seq is the method of choice to efficiently detect and precisely quantify coding RNAs present in a biological sample under specific circumstances. Accura...
Small RNA-seq Service
Small RNA-seq is the method of choice to investigate the regulatory network of small non-coding RNAs (<200 nt length), including but not limited to miRNA ...
Total RNA-seq Service
Exploring the whole transcriptome allows to gain insight of potential transcriptional and regulatory network mechanisms. With Total RNA-seq services, we wi...
Bioinformatics Data Mining Service
New! Data mining using machine learning (AI) for unique epigenetic data insights Watch the webinar to gain insights on how data mining can be applied ...