Omics Research
Genomics

Sanger Sequencing

Streamline operations with this “Gold Standard of Sequencing” service’s fast turnaround time, quality results, and competitive pricing.

What is Sanger Sequencing?

Sanger Sequencing is the oldest proven process of sequencing regions of DNA by using oligonucleotide primers and chain termination.

It is commonly selected to sequence polymerase chain reaction (PCR) products, plasmid DNA, and bacterial artificial chromosomes (BAC).

Why is Studying Sanger Sequencing Important?

The original sequencing method preceding NGS, Sanger sequencing is still useful as a low-cost, high accuracy method for interrogating small DNA regions in a limited number of samples.

What Can You Do?

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Confirm Clones

Verify correct insertion and orientation into plasmid and bacterial artificial chromosome (BAC) backbones.

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Use Capillary Electrophoresis

Get quicker, more accurate services via automated capillary electrophoresis sequencing (CES).

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Access Sequencing Expertise

Enlist Psomagen’s expert help as needed before, during, and after service.

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Get Simplified Ordering

Learn how Psomagen’s barcode-based ordering system reduces form fills.

Tools for Sanger Sequencing

Standard Sanger Sequencing

Best for:
Successfully sequencing samples (premixed or as separate template/primer) including PCR products, plasmids, and BACs in single tubes or 96-well plates
Benefits:
State-of-the-art robotics and instrumentation deliver fast turnaround times, quality results, and competitive pricing

Custom Sanger Sequencing

Best for:
Projects such as 16S rRNA and primer walking
Benefits:
Thanks to 20 years of know-how, a large genomics facility, and advanced DNA sequencing technology (ABI 3730s), you get high-quality sequencing data for projects, large and small

EZ-Seq Sample Labeling

Best for:
Simplifying your DNA sequencing order for premixed samples.
Benefits:
Pre-paid, barcode label-based ordering system means you can get rapid processing and data generation without inputting lines and lines of information on an order form

Quotes From Our Clients

"Their service is always on time. They are super patient with orders."

Rajav Soni

Manufacturing Associate
Moderna

"It's my great pleasure to use them. I've been a customer of Psomagen for a long time and for all of my supplies. I cannot express in words how satisfied I am. My orders are always on time and the staff services are so friendly and efficient. They are very helpful when I have questions and are generous with giving any kind of information. I appreciate Psomagen sequencing and all they do for me. I hope we will be together for our whole tenure. They definitely did a wonderful job!"

Amit Kumar Singh, Ph.D.

NCI/NIH

"I have used Psomagen for sequencing my clones for a site-directed mutagenesis screen. I enjoy the speed of delivery and the fact that I get my results before I wake up the next day. Customer care is present to answer all questions and is quick to resolve issues. I believe this is value for the money."

Samuel Adeleye

Researcher
Rutgers University, New-Brunswick

Ready for the Next Step?

Here's a little information on our ordering process.

If you're already a customer, you can skip to ordering by clicking below.

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Request a Consultation or Quote

Get in touch with your local field team and start designing a project. We’ll help drive your research forward with the right tools for your investigative needs.

Let's Talk!

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Create, Manage and Track Your Project

At this step you'll be able to keep an eye on all the various methods and platforms we’re using to ensure your starting material will produce the most in-depth information possible. It’s easy to get in touch with us if you have a question or concern.

Reach Out!

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Get Your Data and Analysis Reports

Securely access your raw data and view detailed analyses specific to your scientific question all in one place. Then reach out to our bioinformatics scientists to dig deeper into the results.

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Go to Our Customer Portal

Ready to get started on a new project or check in on an existing one? Do that — and more in our customer portal.

Let's Go!

Just Say PSO!

Do you need rapid, accurate Sanger processing that is competitively priced?

Step One Sanger, Step Two NGS

While Sanger sequencing is tried and true, some projects require the massively parallel sequencing provided by our NGS offerings.

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Whole-Genome Sequencing

The best way to gain insight into the entire DNA sequence. Select rapid, accurate CAP/CLIA or RUO whole-genome NGS for the widest coverage of both coding and noncoding regions

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Whole Exome Sequencing

A way to study the 2% of the genome that contains 85% of known genetic variants. Gain efficiency through top tools and technologies that focus on the exome, a key player in numerous disease states.

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Targeted Sequencing

For investigating a specific region of DNA or asking a pointed research question. Choose advanced solutions for targeted sequencing including amplicon and hybrid capture technologies.

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RNA Sequencing

How to access the wealth of data in “the other nucleic acid.” Look to the transcriptome for a more direct view of what is being expressed and affecting patient health.