AmpliconSEQ empowers your research with high-precision, targeted NGS for actionable genetic insights. Achieve faster results, lower costs, and unmatched sensitivity—tailored to your exact needs.
Amplicon sequencing (AmpliconSEQ) is a high-precision next-generation sequencing (NGS) method designed to analyze specific DNA regions. By selectively amplifying target sequences using PCR before sequencing, AmpliconSEQ enables accurate detection of genetic variations, microbial community profiling, and mutation analysis. 
How AmpliconSEQ Works
→Target Selection & Primer Design – Specific primers are designed to bind to the DNA regions of interest, ensuring precise targeting of genetic sequences.
→PCR Amplification – The selected regions are amplified using polymerase chain reaction (PCR), generating high-quality DNA fragments for sequencing.
→Library Preparation – Unique sequencing adapters and barcodes are added to the amplified DNA, allowing for multiplexing and efficient sequencing.
→Next-Generation Sequencing (NGS) – The prepared libraries are loaded onto an NGS platform, where millions of DNA fragments are sequenced in parallel.
→Data Processing & Analysis – Bioinformatics tools process the raw sequencing data to identify genetic variations, mutations, or microbial species composition.
Why Choose AmpliconSEQ?
- Cost-Effective – Focuses on relevant genomic regions, reducing sequencing costs.
- High Sensitivity – Enables ultra-deep sequencing to detect low-frequency variants.
- Comprehensive Coverage – Analyzes hundreds to thousands of amplicons in a single run.
- Versatile – Adaptable for applications such as microbial diversity studies and genetic variant detection.
- Fast & Efficient – Provides rapid turnaround times for results.
At Hy Laboratories, we specialize in providing expert-driven AmpliconSEQ solutions tailored to your research needs. Contact us today to learn how our advanced sequencing services can enhance your genetic studies!
For more information: Dr. Ronen Hoff
ronenh@hylabs.co.il | 054-6610304