Software
Multiple Applications
Investigate genetic variations for NGS-based panels from various kit and machine manufacturers.
Medical Guideline
Comply with S1-Guideline by the German Society of Human Genetics (GfH) during analysis and quality control
Local Installation
Deploy the software locally, allowing usage with stringent regulatory compliances and security requirements.
Features
Save time and effort
The software is optimized for fast and automated routine usage in diagnostic labs. Our end-to-end software moves you rapidly from data generation to interpretation.
Stringent Quality Control
Seamless NGS gives you all measures to assess the quality of each sample quickly and intuitively. Tracking of quality of certain panels/protocols over time allows you to evaluate your wet lab efforts.
Clear Result Presentation
Comprehensive information about DNA variants, their annotation and effects is directly available. Various sorting and filtering options enable fast result interpretation.
Interactive Data Exploration
Intuitive sequence visualization has been tighly integrated into Seamless NGS to help with reducing false postives and increasing certainity in problematic variant calls.
Streamlined Variant Interpretation
Assign own pathogenicity classifications to easily keep track of observed variants. New variants can be ranked according to historical classifications and include a complete audit trail.
Feature Overview
| Push-Button Analysis | High Data Security and Privacy | ||
| Up to 50% Time Saving per Sample | Enhanced Quality Control | ||
| In-House Variant Database | Clear Visualization | ||
| Easy-To-Use with Large Gene Panels | Highly Customizable | ||
| Professional Bioinformatics Support | Following the S1-Guideline (by GfH) |
