RNA sequencing (RNA-Seq) technology enables rapid profiling and deep investigation of the transcriptome, for any species. This approach offers a number of advantages compared to microarray analysis, a legacy technology often used in gene expression studies.
Benefits of RNA-Seq vs microarrays
Many researchers start their NGS journey with RNA sequencing, which provides insight into gene expression levels across sample types. This video provides a high-level overview of the RNA sequencing workflow.
"mRNA-Seq offers improved specificity, so it’s better at detecting transcripts, and specifically isoforms, than microarrays. It’s also more sensitive in detecting differential expression and offers increased dynamic range."
This animated video takes you through the Illumina total RNA sequencing workflow covering the advantages of RNA-Seq over other RNA analysis methods, such as qPCR and gene expression arrays. Discover why RNA-Seq is a powerful sequencing method for visibility into previously undetectable changes in gene expression.
If NGS is a good fit for you, the next steps are to consider which applications and methods you’d like to perform, and choose an instrument that matches your expected output and application needs.
Thanks to its scale and unbiased discovery power, researchers can use NGS in a variety of basic and translational research areas. By providing a deeper view into a variety of biological systems using diverse sample types, you can expand the scope of your studies and find the answers to your boldest research applications.
The portion of NIH grant funding allocated to new RNA sequencing vs gene expression microarray-inclusive grants has been trending towards RNA-Seq technology for the last several years. Publication trends demonstrate the rapid adoption and increasing impact of RNA-Seq–based research.
This video covers key considerations for experiment planning and sample preparation kit options for RNA input.
In the second part of our RNA-Seq video webinar series, we dive into best practices for Illumina RNA kits.
In this webinar, we discuss the user-friendly RNA-Seq analysis options available on BaseSpace, a data management and data analysis hub.
For an in-depth look at NGS compared to to other methods, download our Getting Started with NGS eBook. This eBook outlines key differences, recommended methods/applications, sample workflows, and more.
This eBook highlights discoveries powered by modern transcriptomics and epigenetics methods that are impacting our understanding of biology and disease.
Transcriptomics, the characterization of the complete set or a designated subset of RNA transcripts produced by the genome, is an accessible entry point for using NGS, given its versatility across use cases and well-established workflows.
Benchtop sequencers are a popular way of getting started with NGS. This resource is a great place to learn about benchtop sequencing capabilities, instruments, and popular applications and methods for each.
Sequencing RNA as well as DNA is giving researchers an extra dimension of information, and pointing oncologists towards potential avenues for treatment.
Find simple, customized RNA-Seq workflows and RNA kits for your experiment.
If you have questions about NGS for your specific research focus, we’d love to help. Our specialists can answer any questions and recommend the best solution for your setup.