What Is Genomics?
Genomics is the study of gene sequence and expression of organisms.
Ongoing advancements in sequencing and profiling techniques enable life science professionals to analyze how genes are expressed and interact with the environment and proteins.
Why Is Studying Genomics Important?
Genomics has revolutionized modern research, drug discovery, patient profiling, animal and agricultural science, and therapeutic administration.
It benefits all fields of biological research, especially in oncology, neurology, cardiovascular, and pulmonary indications, and makes precision medicine possible.
What Can You Do?
Identify Basis of Disease
Compare normal and diseased populations to find targets for therapeutic research.
Map Gene Regulation
Determine not only sequence but also interactive regulatory information from both coding and non-coding regions.
Explore the Whole Genome
With massively parallel next-generation sequencing, you can get all the information at once.
Offer Precision Medicine
Introduce new ways to prevent, diagnose, and treat disease on a personalized level.
Genomics Tools
Whether you need a broad overview or a select region of your sample's genetic content, there's a tool for you! We offer the following genomics services:
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
Ph.D. 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
Quotes From Our Clients
More samples, cheaper cost, faster results. What more could we ask for? ...That we get the results back faster than we do for on-campus work is just icing on the cake.
Daniel Deatherage, Ph.D.
University of Texas at Austin
Pricing was very competitive and cheaper than other sequencing providers (mostly academic sequencing core facilities) that I considered. I would definitely use their service again and am lining up my next amplicon library to do so.
Nathan Ahlgren, Ph.D.
Clark University
If there is no index or mismatch index, they notify in advance before sending the final result, and correct the missing/mismatched index through discussion.
Sae Woong Park, Ph.D.
Weill Cornell Medicine
Genomics in Action
More Omics PSOlutions
Of the hundreds of NGS methodologies available, we curate the most productive, efficient, reliable, and reproducible platforms for you.
