What is Sanger Sequencing?

Sanger sequencing, also known as the dideoxy chain termination method, remains the gold standard for DNA sequencing. Developed by Frederick Sanger, this technique uses dideoxynucleotides (ddNTPs) to terminate DNA synthesis at specific points, generating fragments of varying lengths that are separated by capillary electrophoresis to determine the exact order of nucleotides (A, T, C, G).

Despite the rise of Next-Generation Sequencing (NGS), Sanger sequencing continues to be preferred for its unmatched accuracy (99.99%), long reads, simplicity, and cost-effectiveness in small-to-medium scale projects.

Why Choose Sanger Sequencing?

Sanger sequencing is the method of choice when you need:

  • High-accuracy confirmation of variants identified by NGS
  • Long contiguous reads (up to 1000 bp)
  • Sequencing of difficult templates (GC-rich regions, hairpins, repetitive sequences)
  • Low-throughput, targeted sequencing of 1–100 samples
  • Microbial identification and genotyping
  • CRISPR editing validation and plasmid verification

Our Advanced Sanger Sequencing Capabilities

At Yaazh Xenomics, we combine cutting-edge capillary electrophoresis systems with proprietary protocols to deliver superior quality results:

  • Read length: Up to 1000 bases per reaction (higher than standard 800 bp)
  • Excellent performance on challenging templates including GC-rich and hairpin structures
  • High-throughput processing in 96-well format
  • Free universal primers (vector primers) included
  • Expert troubleshooting and free technical consultation with every project

Comprehensive Sanger Sequencing Services We Offer

  • Single-read Sanger DNA sequencing
  • Plasmid sequencing (small & large constructs)
  • PCR product sequencing (purified & unpurified)
  • Primer walking projects
  • Bacterial identification via 16S rRNA sequencing
  • Fungal & Yeast identification via 18S rRNA, ITS, or 26S rDNA
  • Microbial identification services
  • Gene and genomic region re-sequencing
  • Cloning verification (PCR products & DNA fragments)
  • DNA isolation from various sources (including large constructs)
  • Primer design and synthesis
  • PCR amplification and purification
  • Genotyping and DNA fragment analysis
  • Library services (normalized cDNA, shotgun, cosmid/fosmid)

Typical Applications of Our Sanger Sequencing Services

  • Confirmatory sequencing after NGS
  • Clinical & diagnostic variant validation
  • Microbial taxonomy and identification
  • Pharmaceutical and biotech quality control
  • Synthetic biology and construct verification
  • CRISPR-Cas9 editing efficiency analysis
  • Plant, animal, and human genomic research
  • Food safety and environmental microbiology

Why Researchers & Industries Trust Yaazh Xenomics for Sanger Sequencing

  • State-of-the-art facility in Coimbatore with experienced molecular biologists
  • Consistent, publication-ready high-quality data
  • Fast turnaround time with reliable delivery
  • Competitive pricing for academic, industrial, and clinical clients
  • Full support from sample submission to data analysis
  • Seamless integration with other services like NGS, qPCR, and bioinformatics

Exceptional Benefits Of Sanger Sequencing

Assured Quality

We cater to high-quality sequencing of upto 1000 bases/reaction read length as opposed to 800 bases. We leverage cutting-edge and proprietary technology too.

Consistent Results

We deliver consistent, solid data on templated like GC-rich areas, hairpins and more. With Yaazh Xenomics, you can always be assured of precise results.

Dependable Team

We utilise trained team members with universal and free vector primers for DNA analysis. They have the expertise and experience to offer you reliable and accurate data.

Quick Turnaround

We offer you a quick turnaround time, troubleshooting and free advice with each analysis. Whatever be the assistance you need, we will be happy to help.

Quick Sanger DNA Sequencing Process

The samples Yaazh uses for the Sanger DNA sequencing include plasmid, cosmid, genomic DNA, purified PCR products, un-purified PCR products, and single-stranded phage DNA.

01

We use chain termination PCR to make manifold copied of the DNA sequence under observation. Each oligonucleotide copy terminates at random length using a 5’-ddNTP.

02

We perform gel electrophoresis on the DNA samples. On application of a current, the negatively charged oligonucleotides move towards the other end of the gel matrix.

03

We read the gel to determine the DNA sequence of the sample. Because the synthesised DNA direction is 5’ to 3’, every last dideoxy-nucleotide correspond to a specific nucleotide in the original sample. 

Ready to Sequence Your DNA Samples?

Contact our expert team today for a free consultation, custom quote, or sample submission guidelines.

Phone: +91 99431 32020 | +91 95002 45454

Address:
Module No. 103, TICEL BIOPARK Phase – III, 1st Floor,
Maruthamalai Road, Coimbatore - 641046, Tamil Nadu, India

Also serving clients from Visakhapatnam and across India.

Single read sequencing
Microbial identification
Fungal Identification (18S rRNA or ITS)
Bacterial Identification (16S rRNA)
Cloning of PCR products
DNA fragments cloning
Primer walking projects
High-throughput sequencing (MTP in 96 well formats)
Yeast Sequencing (18S or ITS or 26s rDNA)
PCR amplification and purification
Primer design & synthesis
Genes and/or genomic regions re-sequencing
DNA isolation, including large constructs
Small Plasmid & Large Plasmid Sequencing
Library services (normalised cDNA, shotgun, cosmid/fosmid)

The Specialist In Sanger Sequencing

Would you like to avail our expert Sanger DNA sequencing services? Talk to us for professional assistance.

Contact Us
Yaazh Xenomics,
Module No. 103,
TICEL BIOPARK Phase – III,
1st floor, Maruthamalai Road,
Coimbatore - 641046.
Tamil Nadu, India
Yaazh Xenomics,
No.9-6, Sritej Nagar,
Anandapuram,
Visakhapatnam -531022.
Andhra Pradesh
Yaazh Xenomics,
Ground Floor, Plot No.17-R1,
120 feet Road,
Vivekananda Nagar,
Sambakulam, Madurai - 625 007,
Tamil Nadu. Indi

Yaazh Xenomics is a leading biotechnology company based in Coimbatore, Tamil Nadu, India, specializing in comprehensive genomic solutions. As a DNA testing laboratory, we offer a broad spectrum of services, including DNA sequencing, RNA Sequencing, Sanger Sequencing, 16s rRNA, 18s rRNA, ITS, COI, RBCL, Matk gene Sequencing for DNA Barcoding, gene expression analysis, SNP analysis, Next-Generation Sequencing (NGS), Various Medical Genome testing, Exome Sequencing, Gut Microbiome Test, Metagenome Sequencing, Whole Genome Sequencing (WGS), Transcriptome Sequencing using advance NGS platforms like Nanopore, Illumina, MGI, Thermo. Also, we provide advance Bioinformatics, Customized Bioinformatics and a variety of other genetic testing and Molecular testing.

 

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