Omics Research

Genomics

Unlock the wealth of genetic information revolutionizing the life sciences.

What is Genomics?

Genomics is the study of gene sequence and expression.

Ongoing advancements in sequencing and profiling techniques enable life science professionals to understand 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?

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Identify Basis of Disease

Compare normal and diseased populations to find targets for therapeutic research.

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Map Gene Regulation

Determine not only sequence but also interactive regulatory information.

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Explore the Whole Genome

With massively parallel next-generation sequencing, you can get all the information at once.

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Offer Precision Medicine

Introduce new ways to prevent, diagnose, and treat disease on a personalized level.

Genomics Methods

Whole-Genome Sequencing

Best for:
Insight into the entire DNA sequence, both coding and noncoding regions for basic research, drug discovery, or clinical use.
Benefits:

Rapid, accurate CAP/CLIA or RUO whole-genome NGS provides the widest coverage

Whole-Exome Sequencing

Best for:
Sequencing the 2% of the whole genome that accounts for 85% of known, disease-related genetic variants
Benefits:
Efficient, cost-effective way to identify rare genetic variations and improve diagnostic testing

Targeted Sequencing

Best for:
Sequencing distinct genetic regions of interest rather than the whole genome
Benefits:
In-depth, selective sequencing yields specific insights cost-effectively

Sanger Sequencing

Best for:
Sequencing small DNA regions in a limited number of samples, such as PCR products, plasmid DNA, and BACs
Benefits:
Rapid, highly accurate sequencing that is supported by experts and competitively priced

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

PSO Bold!

How can Psomagen services streamline your next genomics project?

More Omics PSOlutions

Of the hundreds of NGS methodologies available, we curate the most productive, efficient, reliable, and reproducible platforms for you.

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Transcriptomics

A more complete picture of various disease states. Take a closer look at both coding and noncoding RNA — mRNA, smRNA, lncRNA, and more — with a variety of sequencing strategies.

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Metagenomics

A new understanding of the world’s biosphere. Discover the biological diversity in environmental and microbial samples and their evolution and function.

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Epigenomics

More ways to elucidate gene expression. Find solutions such as ATAC and ChIP-seq to further investigate how protein and nucleic acid interact.

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Proteomics

A novel way to predict and understand human illness. Go beyond the nucleic acid map and identify and quantify the protein biomarkers that are the hallmarks of disease.