Seamless NGS is a software platform for automated analysis and management of next-generation sequencing experiments. It provides easy access to advanced bioinformatics protocols for the detection of SNVs, InDels, Copy Number Variants and RNA Fusions.
Investigate genetic variations for NGS-based panels from various kit and machine manufacturers.
Comply with S1-Guideline by the German Society of Human Genetics (GfH) during analysis and quality control
Deploy the software locally, allowing usage with stringent regulatory compliances and security requirements.
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.
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.
Comprehensive information about DNA variants, their annotation and effects is directly available. Various sorting and filtering options enable fast result interpretation.
Intuitive sequence visualization has been tighly integrated into Seamless NGS to help with reducing false postives and increasing certainity in problematic variant calls.
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.
|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)|
The BRCA1/2 analysis workflow in the Seamless NGS software convinced us with its ease of use and the fast evaluation of the detected variants. We participated successfully in a QuIP round-robin test, achieving a full score (20/20 points), thus confirming the high accuracy of the genetic testing software. Therefore, Seamless NGS is a qualified data analysis tool. With its help, we could successfully establish NGS-based BRCA1/2 testing in our routine diagnostics.