Security & Data Storage
MASTR Reporter
It provides optimized, automated, and simultaneous variant calling of SNVs, indels, and CNVs to ultimately provide the correct results. In addition, it provides a user-friendly dashboard to review quality of the entire workflow. MASTR Reporter is available for both somatic and germline use.
- NGS Software
Product Details
- Online application: Easily access through encrypted connection with web browser
- Simple workflow: From DNA sample to report
- High quality data: Integrated quality control to measure, monitor and optimize your complete workflow
- Reliable variant calls: All software parameters are optimized specifically for SureMASTR panels enabling fast and reliable variant calling (SNVs, indels and CNVs)
- Transparent data analysis: Layered information from variant to sequencing reads, which allows for deep analysis of the data
- Metrics and analytics: For traceability and audits
- Safe data: Stringent data security. Software developed with ISO 13485 and IEC 62304 compliance
- Automation of the analysis and interpretation: Automatic upload from the sequence server to MASTR Reporter and from MASTR Reporter to Alissa Interpret is possible
- Customizable filtering: Restrict analysis results to a selection of genes or screening variants, quickly and cost-effectively
Our Technology
Recent advances in various areas of clinical medicine, diagnostics and genetic testing have created a significant opportunity for the development of high value genetic tests to enable the practice of personalized medicine.The availability of affordable Next-Generation Sequencing systems provides the foundation on which PCR based technologies can be applied to address a wide range of unmet needs.
Learn MoreMultiplex PCR
Multiplex PCR is a molecular biology technique for the amplification of multiple genomic targets in a single PCR experiment.
Learn MoreMASTR: Multiplex Amplification of Specific Targets for Resequencing
MASTR assays offer an innovative combination of premixed PCR primers in a ready-to-use kit, enabling enhanced target amplification for DNA-based diagnostics.
Learn More- Brochures
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SureMASTR Assays General brochure US/CA/ROW
The Ready-to-use SureMASTR catalog assays analyze the genes that matter in a simple, efficient and reliable way.
- Brochures
- English
- 22 Oct 2018
- 2.85 MB
MASTR Reporter Brochure 5991-9314EN
MASTR Reporter Analysis solution for SureMASTR assays
- Brochures
- English
- 22 Oct 2018
- 1.83 MB
- FAQs
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MAQ-S
Tool for automated analysis of data generated with our Multiplex Amplicon Quantification (MAQ) assays.
MAQ Design
Tool to assist you in developing a personal MAQ assay to analyze your CNV region of interest.
Thomas von Känel
Chef du Service de Génétique Médicale,, Hôpital du Valais, Switserland
"CNV detection can reveal potential testing pitfalls like allelic dropouts! Here, MASTR Reporter gave two clear deletion signals in BRCA1/2. MLPA did not reveal a CNV. Sanger sequencing identified two rare variants in the primer binding sites of the NGS reactions but did not reveal a pathogenic variant in the alleles that were not amplified in the NGS testing."
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