See what's possible with third generation sequencing technologies. With long-read sequencing, it's easier than ever to access large, complex DNA and RNA regions.
What Can You Do?
Comprehensive Genome Assembly
Reconstruct or generate de novo genomes with fewer errors and areas of uncertainty, even in areas of high homology.
Obtain a complete and accurate representation of each copy of the genome or region of interest.
Reach difficult to detect genomic regions, like high GC regions or large insertion-deletion areas. Link phenotypes to novel genes and causative variants.
Get methylation data from your sample without extra steps or protocols. Take simultaneous advantage of haplotype-phased and variant-called genomic information.
Long-Read Best Practices
We accept numerous sample types for our long-read technology, not limited to:
- Cultured cells and bacteria
Regardless of the starting material, it is possible to attain high quality, accurate results. We also offer extraction services for your convenience.
Each SMRT Cell can produce up to 90 Gb of total long-read sequencing data, a phased 30x whole human genome, up to 80 million full-length RNA isoforms, and approximately 170 HQ-MAGs from a human gut microbiome sample.
Standard report includes sequence data and QC results. Depending on your needs, we can include variant calling, mapped files, methylation information and more.
Why Our Clients Choose Psomagen
Superior Data Quality
Exceeds manufacturer benchmarks
Starting at one week for sequencing projects
Sequencing and customer support in Rockville, MD
Ph.D. Level Support
Expert assistance every step of the way, with real-time project updates through our online system
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