RNA sequencing (RNA-Seq) is revolutionizing the study of the transcriptome. A highly sensitive and accurate tool for measuring expression across the transcriptome, it is providing researchers with visibility into previously undetected changes occurring in disease states, in response to therapeutics, under different environmental conditions, and across a broad range of other study designs.
RNA-Seq allows researchers to detect both known and novel features in a single assay, enabling the detection of transcript isoforms, gene fusions, single nucleotide variants, and other features without the limitation of prior knowledge.
RNA-Seq with next-generation sequencing (NGS) is increasingly the method of choice for researchers studying the transcriptome. It offers numerous advantages over gene expression arrays.
Find out how Illumina NGS technology works and what types of experiments it enables.
Learn about 7 key RNA-Seq methods. Find out how they differ to help you determine the method most appropriate for your research.
A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
Generate RNA-Seq protocols tailored to your specific workflow.
Delivers the power of high-throughput sequencing with the speed, simplicity, and affordability of a benchtop instrument.
Researchers are using RNA-Seq to reveal how lncRNAs could be used to identify, measure, and treat cancer.Read Customer Interview
Researchers are using 16sRNA to investigate the genomes of microbes and improve our understanding of human health, disease, and microbial evolution.Read Interview
Learn about read length and depth requirements for RNA-Seq and find resources to help with experimental design.Read Technical Bulletin
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