Precision Genomics for Clinical Confidence
The IVDNGS™ Clinical NGS Panel and Library Preparation Kit is a comprehensive, high-performance solution designed for clinical next-generation sequencing (NGS) applications. Developed for in vitro diagnostic (IVD) use, this kit enables accurate detection of clinically relevant mutations, gene fusions, copy number variations, and more — empowering clinicians with actionable insights for personalized medicine.
From sample to sequencing-ready libraries, the IVDNGS™ kit ensures optimal performance, high sensitivity, and reproducibility across a broad range of clinical samples, including FFPE tissue, blood, and cfDNA.
Targeted NGS panels for oncology, hereditary diseases, and infectious disease diagnostics
Streamlined library prep protocol with minimal hands-on time
High coverage uniformity and sequencing depth
Compatible with Illumina® and Ion Torrent™ platforms
Includes validated primer sets, enzymes, and index adapters
Designed under ISO13485 and IVD guidelines for clinical reliability
Cancer Genomics (Solid Tumors, Liquid Biopsy)
Hereditary Disease Testing (BRCA1/2, Cardiomyopathies, etc.)
Pharmacogenomics
Pathogen Detection & Surveillance
Rare Disease Research
| Parameter | Details |
|---|---|
| Input DNA/RNA | 10–200 ng (depends on panel) |
| Sample Types | FFPE, blood, saliva, cfDNA, fresh frozen tissue |
| Turnaround Time | 6–8 hours (library prep) |
| Panel Types | Pre-designed & customizable targeted panels |
| Platform Compatibility | Illumina®, Ion Torrent™ |
| Storage Conditions | -20°C |
| Shelf Life | Up to 12 months |
| Certifications | IVD compliant, ISO13485 certified |
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