It provides an end-to-end INLab solution, from sample preparation to automated data analysis, enabling fast, accurate, and cost-effective genetic testing. Key Features & Technologies 1. Embedded NGS System: Combines sequencing, bioinformatics, and reporting in a single streamlined platform. 2.Fully Automated Workflow: Reduces human error and increases efficiency by automating sample preparation, sequencing, and data interpretation. 3.Scalable Throughput: Supports various sequencing volumes, making it suitable for small labs and large-scale clinical settings. 4.Integrated Quality Control: Ensures high-precision sequencing with real-time monitoring of sample integrity and sequencing performance. The INLab NGS Solution is ideal for: 1.Leukemia and Oncology Precision Medicine: Accelerates the identification of actionable mutations for personalized treatment strategies. 2.Clinical Diagnostics: Provides rapid and reliable genetic insights to support medical decision-making. 3.Pharmaceutical R&D: Enhances drug development and companion diagnostics through deep genomic analysis. 4.Decentralized Testing: Enables hospital-based and lab-based NGS testing, reducing reliance on centralized sequencing facilities. Problems Solved 1.Delays in Diagnosis: Significantly shortens turnaround time, allowing clinicians to make faster treatment decisions. 2.Complex NGS Data Interpretation: One-click NGS analysis software simplifies the analysis, making it accessible to non-bioinformatics experts. 3.High Costs of NGS: An embedded, cost-efficient solution that lowers operational and reagent costs. 4.Scalability & Accessibility: Bridges the gap between centralized and decentralized testing by making NGS technology more accessible to hospitals and research centers. With INLab NGS Solution, precision medicine is now faster, smarter, and more accessible, transforming how genetic testing is performed for better patient outcomes