Contact us

MICK ClinicalTM

Cloud IVD Software for Gastrointestinal Pathogens

Bring speed and clarity to gastrointestinal pathogen screening with a cloud-based CE-IVD software solution, compliant with the IVDR.

Book a demo
Contact us
overview

Automated NGS-based screening for selected gastrointestinal pathogens

MICK Clinical is a CE-marked in vitro diagnostic (IVD) cloud software supporting laboratories and healthcare institutions with efficient screening of selected gastrointestinal microorganisms.

By automating the analysis of raw sequencing data, MICK Clinical enables:

Efficient screening

One workflow supports the screening of multiple selected gastrointestinal microorganisms in a single report.

No added manual workload as testing volumes increase.

Earlier insights compared to sequential testing approaches.

Why NGS?

Main value of using NGS

Tap each category to compare methods

Pathogen Coverage

Traditional

Limited to predefined targets (one panel at a time)

NGS

Broad, comprehensive detection of multiple pathogens in a single run

Traditional

Multiple sequential tests may be needed

NGS

One workflow covers many organisms simultaneously

Traditional

Reliable but can be slower if multiple tests are required

NGS

Streamlined, faster overall diagnosis process

Add Your Heading Text Here

Pathogen Coverage

Workflow Efficiency

Turnaround Time

Traditional Methods (PCR / Culture)

Limited to predefined targets (one panel at a time)

Multiple sequential tests may be needed

Reliable but can be slower if multiple tests are required

Next-Generation Sequencing (NGS)

Screening of key selected pathogens within a single workflow

Scales with high-throughput NGS workflows

Streamlined, faster overall diagnosis process

KEY FEATURES

Reasons why you should work with MICK CLINICALTM

Seamless workflow integration

Easily integrates into existing NGS workflows, removing slow manual data handling.

Clinically validated

Demonstrated an overall sensitivity of 91.7% and specificity of 99.5% in a clinical validation study.

Rapid turnaround

Delivers reliable results within hours, accelerating decision-making.

Secure by design

Developed under GDPR framework, and hosted on ISO 27001– and SOC 2–compliant cloud infrastructure.

Clinical Context

Clinically validated.
Performance you can trust

MICK Clinical has been clinically validated to support reliable screening of key gastrointestinal microorganisms. In a clinical validation study, the software demonstrated an overall sensitivity of 91.7% and a specificity of 99.5%, confirming its strong clinical performance.

Designed for routine clinical laboratory use

Supports diagnosis by providing clear, standardised screening results for gastrointestinal pathogens.

Automation-driven workflow

Seamlessly integrates into NGS workflows using raw FASTQ data from faecal samples.

IVDR-ready and CE-marked

Developed and validated in accordance with Regulation (EU) 2017/746 (IVDR) for in vitro diagnostic medical devices.

MICK Clinical™ is intended for professional use only. The test has been validated for use in symptomatic individuals aged 18-64. MICK Clinical™ is not intended for comprehensive virulence gene detection.

Compliance & Security

Built on recognised security standards to protect data and ensure compliance.

Our compliance with the General Data Protection Regulation (GDPR, EU 2016/679) ensures that all personal data are processed lawfully, transparently, and securely, in accordance with the highest standards of privacy and data protection.

Our accreditation according to the ISO 13485:2016 standard ensures that the design, development, production, and distribution of medical devices comply with the highest quality and safety standards.

ISO 13485:2016 Certified by Notified Body TÜV SÜD Product Service GmbH (NB 0123).

CE 0123 - Edited

Our CE-IVD marking certifies that MICK CLINICAL comply with the European Union’s strict regulatory requirements for safety, performance, and reliability.

CE-IVD conformity assessed according to Regulation (EU) 2017/746 (IVDR). Certified by Notified Body TÜV SÜD Product Service GmbH (NB 0123).

publications

MICK CLINICALTM trusted in scientific research and peer-reviewed publications

View all publications

A Comprehensive Benchmark of GAIA 3 for 16S rRNA Taxonomic Classification

Read more

Impact of live black soldier fly larvae supplementation on laying hen performance, stress levels and excreta microbiota

Read more

MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing

Read more

ALWAYS AHEAD

Ready to enhance your analysis with MICK CLINICALTM?

Request a demo

Your Questions Answered

Genome assembly

The complexity of genomes (human and non-human), which requires exceptional analytical power.

The heterogeneity and variable quality of omics data, along with the lack of standardized protocols.

The need for robust computational tools to process the sheer volume of data from high-throughput technologies.

The difficulty of translating complex data into applicable results tailored to each stakeholder’s unique needs, which demands the highest level of scientific and technical expertise.

Request a demo

Leave us your details and one of our specialists will get in touch with you as soon as possible.

By clicking send, you agree to our Privacy Policy. Sequentia Biotech will use your details to respond to your inquiry and manage the ongoing dialogue with you. You can unsubscribe from marketing communications at any time

Contact our team

Leave us your inquiry, and we will get back to you shortly.

By clicking send, you agree to our Privacy Policy. Sequentia Biotech will use your details to respond to your inquiry and manage the ongoing dialogue with you. You can unsubscribe from marketing communications at any time

Speak to a specialist

Leave us your details and one of our specialists will get in touch with you as soon as possible.

By clicking send, you agree to our Privacy Policy. Sequentia Biotech will use your details to respond to your inquiry and manage the ongoing dialogue with you. You can unsubscribe from marketing communications at any time

Speak to a specialist

Leave us your details and one of our specialists will get in touch with you as soon as possible.

By clicking send, you agree to our Privacy Policy. Sequentia Biotech will use your details to respond to your inquiry and manage the ongoing dialogue with you. You can unsubscribe from marketing communications at any time