What Is Next-Generation Sequencing?
Next-generation sequencing moves beyond what's possible for Sanger sequencing with massively parallel, high-throughput technology. The development of this technology has made it faster, more affordable, and more accessible for accurate profiling of the genome, transcriptome, or proteome.
Whether you're exploring methylation, DNA-protein interactions, genetic variants, RNA splicing, or the microbiome, there's an NGS tool for you!
Why Is NGS Important?
Cost-effective NGS has aided research and clinical applications, particularly when we have no prior knowledge about the sample. NGS makes it possible to analyze genomes at a new level that enhances the capabilities of scientific research.
What Can You Do?
Get High-Throughput Results
Read more DNA base pairs in less time and at a lower cost than with Sanger sequencing.
Identify Basis of Disease
Compare normal and diseased populations to find targets for therapeutic research.
Investigate Biology at Multiple Levels
Explore elements of the genome, transcriptome, or proteome for the insights your project needs.
Develop Therapeutics
Identify disease biomarkers and gain valuable insights for translational research.
On-Going Promotions
We're always adding new deals — check in often for updated promotions!
Why Our Clients Choose Psomagen
Superior Data Quality
Exceeds manufacturer benchmarks
Fast Turnaround
Starting at one week for sequencing projects
US-Based Processing
Sequencing and customer support in Rockville, MD
PhD-Level Support
Expert assistance every step of the way, with real-time project updates through our online system
Automated Workflows
Increase scalability and improve reproducibility
CLIA-Certified, CAP-Accredited Labs
Clinical research options available (inquire for more information)
Complete Sequencing Solutions
From extraction to data analysis, with many sample types accepted
