Next-Generation Sequencing (NGS)
Unlocking Genomic Insights for Precision Science
Our Next-Generation Sequencing (NGS) platform empowers cutting-edge research, diagnostics, and discovery through high-throughput, accurate, and data-rich genomic analysis. By decoding DNA and RNA at unprecedented speed and scale, we enable scientists, clinicians, and innovators to uncover genetic variations that drive health, disease, and human diversity.
Our integrated bioinformatics pipeline ensures high-quality data interpretation — from variant calling to annotation and visualization. We translate complex genomic data into clinically and scientifically meaningful insights, empowering faster decision-making and impactful research outcomes.
Every sequencing project is conducted under strict quality control protocols, ensuring accuracy, reproducibility, and regulatory compliance. Our processes adhere to international standards in genomic research and clinical validation.
What We Do
We utilize advanced sequencing technologies to deliver comprehensive genomic insights that support everything from medical diagnostics to translational and forensic research.
- Whole Genome Sequencing (WGS): Comprehensive analysis of an organism’s entire genetic makeup to identify mutations, variants, and hereditary patterns.
- Whole Exome Sequencing (WES): Targeted sequencing of protein-coding regions to pinpoint disease-causing mutations.
- Targeted Gene Panels: Focused analysis of specific genes associated with known diseases or traits for clinical and research applications.
- Transcriptome (RNA) Sequencing: Understanding gene expression and regulation in various biological and disease contexts.
- Metagenomics & Microbiome Studies: Exploring microbial diversity and its impact on health and environment.
Powering Discovery and Innovation
NGS is transforming how we approach medicine, biology, and forensic science. Our sequencing solutions support a wide range of applications, including:
- Disease gene discovery and clinical diagnostics
- Personalized and precision medicine
- Biomarker identification and drug development
- Forensic DNA profiling and human identification
- Agricultural and environmental genomics
Frequently Asked Questions
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1.What is Next-Generation Sequencing (NGS)?
Next-Generation Sequencing (NGS) is an advanced DNA and RNA sequencing technology that allows millions of genetic fragments to be analyzed simultaneously. It provides comprehensive insights into genetic variations, mutations, and expression patterns—making it a cornerstone of modern genomics, diagnostics, and research.
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2.How does NGS differ from traditional sequencing methods?
Unlike traditional Sanger sequencing, which processes one DNA fragment at a time, NGS can sequence millions of fragments in parallel. This results in faster turnaround times, higher accuracy, and lower costs per sample—enabling large-scale genomic studies and personalized medicine applications.
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3.How accurate and reliable are NGS results?
Our sequencing workflows follow international quality standards and include multiple layers of validation to ensure accuracy, reproducibility, and traceability. Data quality metrics such as read depth, coverage, and variant accuracy are continuously monitored for every run.
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4.Can NGS be used for clinical diagnostics?
Yes. NGS is widely used in clinical genetics and precision medicine to detect hereditary conditions, guide targeted therapies, and monitor disease progression. All clinical sequencing is performed under strict ethical and regulatory compliance to ensure patient safety and data integrity.