Next-Generation Sequencing

What is Next Generation Sequencing?

Next Generation Sequencing (NGS) is a modern sequencing technology that enables the rapid and parallel sequencing of genetic material with high precision. Compared to traditional methods, NGS is faster, more cost-effective, and capable of generating massive volumes of data. With this technology, millions of DNA or RNA molecules can be sequenced simultaneously.

High-Throughput Data Generation: Millions of reads can be produced in a single run.
Time and Cost Efficiency: Offers faster results at a lower cost than conventional methods.
Broad Range of Applications: Enables genomic, transcriptomic, epigenetic, and metagenomic studies.
High Accuracy and Sensitivity: Detects even rare variants with high precision.
Personalized Medicine: Supports patient-specific diagnosis and treatment planning, especially in cancer and rare diseases.

Advantages of Our NGS Service

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What is Next Generation Sequencing Application Areas

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Clinical Genomics: Detection of disease-causing mutations and genetic disorders
Viral and Microbial Genome Analysis: Outbreak tracking, variant detection, and metagenomic profiling
Transcriptome Analysis (RNA-Seq): Gene expression profiling, alternative splicing, and lncRNA discovery
Cancer Research: Somatic mutation screening and targeted therapy development
Agricultural and Livestock Genomics: Genetic diversity analysis and species identification
Forensic and Population Genetics: Individual identification, ancestry, and population structure studies

Why Choose us

Specialist in aviding clients of financial challenges

Expertise You Can Trust

✅ Experienced team in molecular biology and bioinformatics

Powerful Infrastructure

✅ High-capacity sequencing platforms and robust infrastructure

Flexible Analysis Solutions

✅ Customizable analysis packages for clinical and research needs

Rapid & Reliable Delivery

✅ Fast turnaround time and reliable reporting

All Your Questions Answered About Our NGS Service!

We accept a wide variety of sample types including blood, tissue (fresh or FFPE), saliva, buccal swabs, viral RNA, bacterial cultures, and environmental DNA. Sample preparation requirements are shared in our submission guidelines.

For standard library prep, we usually require 50–200 ng of high-quality nucleic acid. For low-input or degraded samples (e.g., FFPE), optimized protocols are available—please contact us before submitting.

Exome sequencing is used to diagnose a wide range of genetic-based diseases. These include:
✔️ Rare Genetic Disorders: Diseases that manifest from birth or have a genetic origin
✔️ Cancer Genetics: Investigating the relationship between genetic mutations and cancer
✔️ Neurological Disorders: Neurodegenerative diseases like Alzheimer’s and Parkinson’s
✔️ Hereditary Metabolic Disorders: Diseases like phenylketonuria and albinism
✔️ Vision and Hearing Loss: Genetic-related vision or hearing impairments

Exome sequencing usually takes between 3 to 6 weeks to complete. After sample collection, DNA preparation, sequencing, and bioinformatics analysis take time. Additionally, quality control steps are implemented to ensure the accuracy of the results. The results are delivered to you in the specified format as soon as possible.

WGS results are delivered in the following formats:
✔️ FASTQ: Raw sequencing data
✔️ BAM: Mapped genome data
✔️ VCF: Variant (mutation) analysis file Additionally, bioinformatics analysis reports and interpreted genetic data can be provided upon request.