DNA Sequencing Services in India
End-to-End, High-throughput DNA sequencing workflows - fast TAT, superior data quality, advanced bioinformatics, and free consultation for every step of your research.
What is DNA Sequencing?
DNA sequencing determines the exact order of nucleotide bases (A, G, C, and T) in a DNA molecule. From single-gene sequencing to whole genomes, finding genetic variations is the key to disease studies, evolutionary biology, and personalized healthcare.
Our DNA Sequencing Methods & Technologies
- Sanger Sequencing – Gold Standard for PrecisionTargeted sequencing for known regions, gene fragments and clone inserts. Industry optimized for fast turnaround high quality reads.
- 96-Well Plate High-Throughput SequencingAutomated error free robotic liquid handling pipelines for large scale 96 well plate projects.
- Hybrid & Long-Read DNA SequencingCombining easy short reads with long accurate reads (PacBio/Nanopore) for de novo assemblies, resolving repetitive regions and structural variations.
End-to-End DNA Sequencing Workflow
Consultation & Design
Free project consultation (Sanger vs NGS), experimental design and budgeting.
Sample Prep & QC
DNA extraction from diverse sample types and stringent QC checks.
Library Prep
Library construction and precise quantification.
Sequencing
Sanger reads on ABI 3730xl, NGS on Illumina NovaSeq/MGI/PacBio platforms.
Data Analysis
Primary, secondary (alignment, variant calling) and tertiary (interpretation) analysis.
Delivery & Support
Raw data, final reports and post-delivery consultation.
Sanger vs. NGS: Which Method?
Sanger Sequencing Advantages
- High accuracy for short sequences (~1000 bp)
- Fast turnaround time (24-48 hours)
- Cost-effective for small scale projects
- Best for validating known variants
When to Choose NGS Over Sanger
- High-throughput scale (millions of sequences)
- Whole genome, exome, metagenomics
- Unbiased discovery of novel variants
Applications of Our Services
Why Choose Yaazh Xenomics?
- Ph.D. scientists providing free consultation on experimental design
- Fastest TAT in India (Sanger: 24-48h, NGS: 3-5 weeks)
- ISO 9001:2015 & NABL Compliant state-of-the-art lab in Tamil Nadu
- Transparent pricing with no hidden costs
Sanger Sequencing
Rapid, highly accurate reads for plasmid verification, PCR products, and simple sequences.
De Novo Sequencing
Assembling genomes from scratch using advanced long-read technologies like PacBio.
Difficult Templates
Specialized protocols for GC-rich, repetitive, or secondary structure-heavy DNA.
Get Your DNA Sequencing Project Started
Include us early in the loop for free project consultation. Let our experts design your study.
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