With its exceptional accuracy and unbiased lens, researchers are shifting to NGS to expand the scale and discovery power of their genomics studies. Rather than being limited to sequencing one or a few regions at a time, researchers are now able to expand the scope and impact of their experimental studies.
Key advantages of NGS include:
For variant screening studies with a high number of samples, NGS is the most efficient and cost-effective approach for the sequencing of tens to thousands of genes compared to conventional methods.
"When you’re studying something that’s completely new or uncharacterized, you need a much bigger picture. In our project, there was a lot of uncertainty about what mechanisms are influencing our pathways. And given how little we knew about the mechanisms, we needed to use a broader approach like NGS to more fully understand the mechanism in its entirety.”
NGS offers the power to sequence vast amounts of genetic material at a fraction of the time and cost of traditional methods, allowing for deeper exploration in your lab.2-5 Learn more about how NGS compares to the following traditional molecular biology methods:
Illumina NGS combines the power of traditional reading and counting applications. Identify full sequences and quantify expression changes in thousands of transcripts in a single assay with NGS.6-10
Curious about using NGS for your research? While adopting a new technology may seem intimidating, we’ve created a comprehensive, yet easy-to-follow guide for bringing NGS into your lab. You’ll learn about NGS methods, workflows, data analysis solutions, and more in this step-by-step guide to getting started with NGS.
Download eBookIf 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.
Benchtop sequencers are a great starting point for new users. They offer features such as operational simplicity, preconfigured data analysis workflows, onboard secondary analysis, and fast workflows for a variety of popular applications such targeted sequencing. Learn more about the types of sequencers and how to choose one.
Learn about the three main steps in the NGS workflow: library preparation, sequencing, and data analysis.
Thanks to technology innovations, NGS is much more affordable. These resources will help you outline all costs and plan your experimental budget.
A comprehensive list of tutorials designed to help you understand key concepts in NGS. With videos, online training, and knowledge articles, we’ll guide you through tips and best practices for library prep, sequencing, and data analysis.
We’d love to discuss your current sequencing methods and see how NGS can complement or replace them. One of our specialists would be happy to discuss your research goals and NGS questions.