Why choose Amplicon Suite?
Targeted design
Amplicon Suite is CE-IVD marked software for fast and accurate variant calling and annotation of NGS data, specifically tailored for our specialized gene panels.
Actionable insights
Amplicon Suite streamlines NGS data analysis, providing a seamless journey from FASTQ files to actionable results through a user-friendly interface, eliminating the need for extensive bioinformatics expertise.
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Key features of Amplicon Suite
Amplicon Suite is certified as an in-vitro diagnostic medical device, complying with EC 98/79/EEC. The software is intended for use withour specialized gene panels.
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User-friendly interface
Navigate the software effortlessly, even without prior bioinformatics experience thanks to is intuitive design.
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Tailored solution
Amplicon Suite is designed to meet the unique requirements of each assay, it incorporates application-specific features, ensuring precision and efficiency.![AS_CNV AS_CNV](https://devyser.com/hubfs/AS_CNV.png)
Comprehensive variant analysis
Provides quality for variant calling and annotation of SNVs, indels and CNVs, ensuring reliable results.
One pipeline for each Devyser product
- Devyser CFTR: Facilitate screening for specific mutations with a pre-defined screening list.
- Devyser Thalassemia: Enhanced CNV calling with two complementary techniques.
- Devyser LynchFAP: Deep dive into pseudogenes and gene conversions of PMS2.
- Devyser BRCA, BRCA PALB2 and HBOC: Separate pipelines to tailor specific needs.
- Devyser FH: Unique listing of polygenic and statin response markers.
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Contact us
Want to know more about Advyser Solid organs or other post-transplant monitoring products?
Complete the form below and we will be in touch promptly.
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Ready to explore the full potential?
Dedicated software makes analyzing test results quick, easy and trouble-free. This means a streamlined, end-to-end process with unmatched reliability and transparency for lab personnel. You can request a personalized demo today and find out how our software can streamline your NGS data analysis.