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Sanger Sequencing
Sanger Sequencing is a cost-effective method for determining the nucleotide sequence of DNA. GENEWIZ Sanger sequencing services are award-winning, providing high-quality results, industry-leading customer service and fast turnaround times at competitive prices. GENEWIZ from Azenta Life Sciences is the partner of choice for academic, pharmaceutical, biotechnology, and government institutions around the world.
We are well-equipped to handle DNA sequencing of all complexities including single tube, high-throughput, direct bacterial colony, or glycerol stock DNA sequencing projects. Our mission is to eliminate bottlenecks, improve productivity, and advance your research progress.
GENEWIZ Sanger Sequencing Service
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Sanger Barcodes and Services
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Sanger-EZ
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Direct Colony Sequencing
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ITR Sequencing
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Primer Walking
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Low Concentration Plasmid Sequencing
▼Pre-Mixed and Pre-Defined Tubes
▼Pre-Mixed and Pre-Defined Plates
▼Primers
▼Primer Walking
Sanger Sequencing Features & Benefits
Clever, Convenient Logistics – Contact us to locate a GENEWIZ dropbox near you for free shipping. GENEWIZ will provide you with suitable logistical resources according to your barcode order and priority choice.
Easy Online Ordering – Simply order sequencing barcodes online in CLIMS or activate and assign available prepaid barcodes while placing your online order in your CLIMS account.
Quick Turnaround Times
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Standard
Data reported next business day after samples are received at GENEWIZ. -
Express
Data reported by 12 pm next business day after sample drop off at your nearest GENEWIZ dropbox*

Sanger Sequencing Quick Tips Guide
Learn from the Sanger experts how you can get the most of your DNA Sequencing. Whether you’re troubleshooting a tough sequencing reaction, perfecting PCR visualization, or learning to clean up and refine your PCR products, these resources are designed to help you get the best results.
• Volume 1: Producing Robust, Single-band PCR Product
• Volume 2: PCR Clean-up of Single-band PCR
• Volume 3: Salvaging Nonspecific PCR Products
• Volume 4: PCR Visualization by Gel Electrophoresis
• Volume 5: Troubleshooting a Bad Sequencing Reaction from a PCR Template

Blog | Troubleshooting DNA Templates with Sanger Sequencing
Sanger sequencing is highly effective for testing small targeted genomic regions and for validating results from NGS. However, as with all sequencing technologies, there are limitations and needs for troubleshooting. Read on to learn about the three basic troubleshooting steps we recommend to start with.

Blog | Ensure Complete Plasmid Validation on Your First Attempt with Oxford Nanopore Sequencing
Explore the cutting-edge realm of genomic research with Oxford Nanopore Sequencing (ONT), and how this innovative Next Generation Sequencing technology offers real-time, long-read capabilities, revolutionizing our approach to decoding genetic information.

Webinar | From Base Pairs to Breakthroughs: Understanding Sanger and Oxford Nanopore Sequencing
While Sanger sequencing remains the gold standard for accurate DNA sequencing, advancements in sequencing technology, such as Oxford Nanopore Technology (ONT), have provided a cost-effective, long-read alternative for analysis. In this workshop, delve into the considerations of each technique and discover how to interpret their resulting sequencing data effectively so you can capture the benefits of both approaches for your specific needs.

Blog | Analyzing Sanger Sequencing Data
The output for Sanger sequencing is typically a chromatogram, also known as a trace or ab1 file, and a text-based sequence file. Although the latter may seem to hold all the relevant information—after all, the point of sequencing is to get a sequence—the former can’t be ignored. Here, we provide a guide to understanding Sanger sequencing data.