Next Generation Sequencing (NGS) has revolutionized genomic research, enabling rapid and high-throughput sequencing of DNA and RNA. This technology allows researchers to analyze entire genomes, transcriptomes, and epigenomes with unprecedented speed and accuracy. NGS is widely used in various fields, including medical research, clinical diagnostics, and personalized medicine. It facilitates the identification of genetic variations, gene expression profiling, and the discovery of novel biomarkers. With its ability to generate vast amounts of data, NGS has become an essential tool for advancing our understanding of genetics and improving healthcare outcomes.
Transcriptome profiling, gene expression, alternative splicing. mRNA/Total RNA
Transcriptomee profiling, gene expression, alternative splicing. mRNA/Total RNA
For profiling miRNAs and other small non-coding RNAs
Targeted 16S/ 18S/ ITS and Shotgun Sequencing
Variant analysis across entire genome
Bacterial, viral, fungal genome assembly and annotatio
Focused on protein-coding region
Custom panels for specific disease pathways or biomarker discovery
We handle the complete workflow so you can focus on discovery
High-quality sample collection and rigorous quality control to ensure reliable results.
Efficient extraction of DNA/RNA to maintain integrity and purity for downstream applications.
Preparation of high-quality libraries tailored to your sequencing needs.
State-of-the-art sequencing using Illumina platforms for accurate and high-throughput data.
Comprehensive data analysis to extract meaningful insights from your sequencing data.
Timely delivery of analyzed data and detailed reports to support your research goals.
Comprehensive bioinformatics solutions that transform raw sequencing data into clear, actionable insights
Your study, your way- customized analysis pipelines for discovery.
From figures to findings- complete support for your publication journey
Integrate exome, transcriptome, and epigenome data for deeper insights
