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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.

test tube 1213

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.



Instructions for use

Enter access code found in the lower right corner of the label on the kit box.

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Download a specific Batch Release Certificate (BRC) below.

Guidelines and handbooks (7)

CFTR - Best Practice Guidelines (EU) (English)


Accessory Pack Devyser CFTR Core version 2018-08-20 (English)


Data Analysis Using GeneMapper 2018-12-10 (English)


Handbook Devyser CFTR 68 EN v2022-06-29 (English)


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 Handbook Devyser CFTR 68 Relative signal assessment 7-B914 (English)

89 kb pdf

Product information (1)

Flyer: Devyser CFTR 68 (English)


Software settings (7)

Fragment Analysis Using ABI PRISM 310_2020-06-15 (English)


Fragment Analysis Using ABI 3730 & 3730xL 2020-06-15 (English)


Fragment Analysis Using ABI 3130 & 3130xL 2020-06-15 (English)


Fragment Analysis Using ABI 3500 & 3500xL 2020-06-15, c2021-01-19 (English)


Devyser CFTR 68 (Sep)_POP7_GM4-5_2020-10-12 ()


Fragment analysis using SeqStudio v2023-02-13 (English)


Devyser Seqstudio Settings v.2022-12-29 (English)

4 kb

Safety data sheets (1)

SDS Devyser FA products 7-A429 v2024-01-10 (English)

569 kb pdf

Data tables (1)

Table: Reported insertions and deletions Devyser CFTR 68_2020-06-11 (English)


Enter access code found in the lower right corner of the label on the kit box.

product card


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.