Sequencing Services

Our Sequencing Services offer comprehensive and high-precision solutions for a variety of applications, including genomic research, diagnostics, and personalized medicine. We specialize in:

Sanger Sequencing – Reliable and accurate for small-scale projects, including gene mutation analysis and variant identification.
Next-Generation Sequencing (NGS) – High-throughput sequencing for whole-genome sequencing, RNA sequencing, exome sequencing, and metagenomics.
Nanopore Sequencing – Real-time, long-read sequencing for complex genomic regions, structural variants, and large genomes.
With advanced bioinformatics support, we provide data analysis, interpretation, and insights, empowering researchers and healthcare professionals to explore the genome in-depth, uncover genetic variations, and drive innovation across multiple industries.

First Generation Sequencing

The approach employed here relies on Sanger sequencing, a method that utilizes chain-termination reactions to decipher DNA sequences. The process entails breaking the DNA into fragments, synthesizing ...
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Second Generation Sequencing

Next-generation sequencing (NGS) is a cutting-edge technology that allows researchers to rapidly sequence DNA and RNA with unprecedented speed and accuracy. Unlike traditional Sanger sequencing, NGS e...
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Third Generation Sequencing

(also known as Oxford Nanopore Sequencing) is a newer and more advanced method of DNA sequencing that offers improved accuracy, faster processing time, and lower cost compared to previous generations ...
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