Amplicon Suite
Amplicon Suite is a standalone software (SW) for the detection of genetic variants in human specimens.
Its intended function is to provide an aid for the diagnosis of various conditions, by means of an evaluation of the specimen and the provision of information about the specimen, including the presence/absence of genetic variants and their functional annotation. Moreover Amplicon Suite can be used for research purposes to analyze data obtained from both commercial and custom molecular diagnostic assays.
From sample to result
Custom analysis
NGS analysis
Amplicon Suite
NGS data analysis
SmartSeq provides integrated analysis of NGS data and develops tools for the analysis, visualisation and exploration of data.
Bioinformatics services
We offer a complete service of custom bioinformatics analysis, database customization and implementation, wet and dry support for RNASeq, metagenomics and SNPs identification.
Sequencing services
SmartSeq team offers to customers both in-house and outsourced NGS sequencing services. Please do not hesitate to contact us for further details.
How does Amplicon Suite work?
For its intended use, Amplicon Suite does not target a specific disease but is rather an aid for diagnosis of several pathologies, both depending on genetic factors or depending on external pathogens influence, such as:
- Breast and ovarian cancer (CE-IVD validated analysis)
- Cystic Fibrosis (CE-IVD validated analysis)
- Thalassemia (CE-IVD validated analysis)
- Familial Hypercholesterolemia
Amplicon Suite operates automatically through a user friendly interface that allows the user to easily upload data, run analysis and explore results.
Downloads
Instructions for use
Enter access code found in the lower right corner of the label on the kit box.
Certificates
Download a specific Batch Release Certificate (BRC) below.
Guidelines and handbooks (7)
Addendum to handbook Devyser SeqStudio allele-specific products 7-B908 v2023-03-30 (English)
489 kb pdf
Addendum to handbook Devyser VeritiPro allele-specific products 7-B906 v2023-03-31 (English)
82 kb pdf
Product information (1)
Software settings (7)
Safety data sheets (1)
Data tables (1)
Enter access code found in the lower right corner of the label on the kit box.
Download a specific Batch Release Certificate (BRC) below.
Addendum to handbook Devyser SeqStudio allele-specific products 7-B908 v2023-03-30 (English)
489 kb pdf
Addendum to handbook Devyser VeritiPro allele-specific products 7-B906 v2023-03-31 (English)
82 kb pdf
Addendum to IFU Devyser allele-specific products VeritiPro 7-B905 v2023-03-31 (English)
110 kb pdf
Addendum to IFU Devyser SeqStudio allele-specific products 7-B907 v2023-03-30 (English)
510 kb pdf
Disclaimer
The following page includes CE-IVD validated products intended for use by healthcare professionals only. These products do not give professional advice; physicians and other healthcare professionals who use these tools should exercise their own clinical judgment as to the information they provide.