Dashboard preview of Digital PCR Geeng Application
Preview du système de validation d'échantillons de l'application
Preview de l'écran de gestion des séries et des runs

Rethinking Precision Medicine Through the Eyes of Biologists

DIAGNOW a comprehensive platform
that empower Biologists Expertise

Design by users for users

Discover Diagnow
What we offer

An intelligent software that assists in interpreting genomic health data.

01

Designed by expert end-users

Who understand the real-world challenges faced by molecular biologists.

02

Fully customizable solution

Tailored to your lab’s specific workflows and needs.

03

A one-stop-shop of biology

Centralizing all your biological data and analysis tools in one place.

04

Plug and Play approach

For easy integration into lab software environments.

Applications

Unlock the Power of DIAGNOW in Your Field of Expertise

Genetic Diseases

Oncology

Infectious Diseases

Biotech

Biopharma

Animal Health

Environment

+ Other field

Genetic Diseases

Oncology

Infectious Diseases

Biotech

Biopharma

Animal Health

Environment

+ Other field

Genetic Diseases

Oncology

Infectious Diseases

Biotech

Biopharma

Animal Health

Environment

+ Other field

Image of a biologist, working on a computer, and an interface that allow user to drop file to consult analysis results
What we know As biologists

What you are facing, we have faced too !

Need of customization

We often feel limited by the tools available

Understanding Complex Analytical Workflow

We know the importance of mastering every step of an analysis, especially when innovating

The deeper the expertise, the harder it is to transmit

We understand that expertise locked in silos creates risks and bottlenecks.

Data fragmentation and accessibility challenges

We manage heterogeneous data scattered across systems, which limits its usability
Diagrams illustrating how Geeng simplifies the comprehension of multichannel data.
Our platform centralizes all your data and makes it more readable and understandable for your teams.
Solution

Features That Solve 
Real Problems

Customization and Modular Workflow Engine

Tailor each step to your lab’s logic — no code needed

Expert DataViz for decision-making

Put your data to work — your way

Automated Traceability

Built-in checkpoints, alerts, and audit trails
Contact Us

Geeng Team

+ 13 COLLABORATORS

co-founder

Dr Alexandra Lespagnol, PhD

Molecular Biologist & Cancer Biology Specialist

CO-founder / CEO

Pr Marie de Tayrac

University Prof. & Hospital Practitioner

CO-founder

Florent Denoual, MSc

Bioinformatician

NEW to digital pcr

Meet the next evolution of interpreting Droplet Digital PCR Data

Continuous monitoring of positive, negative & blank controls

App Screen of the main dashboard of DPCR Application

Automatic pre‑validation to streamline analysis and power each steps

App Screen of the samples validation screen of DPCR Application

Easily monitor your laboratory’s activity and optimize your workflows

App Screen of the listing of the series and runs in cards display

Design your own internal workflows with a user-centered solution. Stay ahead with the freedom to add new kits

App Screen of the listing of the series and runs in cards display
Trusted By
Experts & institutions
01
04
Image of Cedric Pastoret
I particularly value the interface’s intuitive design, which streamlines the analysis of run quality metrics and internal controls, including automated bioinformatics checks. The clear, interactive visualization of variants, enriched by data from public databases and predictive tools, greatly facilitates interpretation. The ability to flag pathogenic variants for direct report integration, with persistent annotation across samples, is a key strength that optimizes our time and enhances focus on novel findings.
Dr Cédric Pastoret
Molecular Biology Lead, Hematology Laboratory
Image of Dr Galibert
The tools developed are highly appreciated by biologists, especially the validation interface, which greatly reduces interpretation time while maintaining high diagnostic quality. This fully integrated solution eliminates redundant data entry and ensures a smooth, coordinated workflow between technicians and biologists. It enhances our diagnostic capacity—crucial in a context where rapid results can significantly reduce the loss of opportunities for patients.
Pr Marie-Dominique Galibert
Head of Cancer Genetic Laboratory
Image of Vincent Thibault
The deployment of this 'intelligent' interface allowed us to recruit staff without prior experience in these techniques, who were quickly trained to perform both technical and biological validation of results. I was personally impressed by how quickly the interface was deployed, as well as by its ease of use and robustness.
Pr Vincent Thibaut
Head of Virology Laboratory
Image of Cedric Pastoret
I particularly value the interface’s intuitive design, which streamlines the analysis of run quality metrics and internal controls, including automated bioinformatics checks. The clear, interactive visualization of variants, enriched by data from public databases and predictive tools, greatly facilitates interpretation. The ability to flag pathogenic variants for direct report integration, with persistent annotation across samples, is a key strength that optimizes our time and enhances focus on novel findings.
Dr Cédric Pastoret
Molecular Biology Lead, Hematology Laboratory
Image of Dr Galibert
The tools developed are highly appreciated by biologists, especially the validation interface, which greatly reduces interpretation time while maintaining high diagnostic quality. This fully integrated solution eliminates redundant data entry and ensures a smooth, coordinated workflow between technicians and biologists. It enhances our diagnostic capacity—crucial in a context where rapid results can significantly reduce the loss of opportunities for patients.
Pr Marie-Dominique Galibert
Head of Cancer Genetic Laboratory

All Platforms. 

Fully Compatible.
Completely Trustworthy.

Intuitive Interface

Design and optimize your workflow with ease.

Analytical Control

Precisely monitor operations and analytical indicators.

Security & Access

HDS or on‑premise hosting, compliant with ISO 27001 and FAIR.

Decision Support

Structured approach for reliable, consistent decisions.

Sample Validation

Validate samples via configurable workflows.

Clinical Monitoring

Track patients and continuously integrate clinical data.

Extensible Testing

Incorporate any genomic test, regardless of supplier.

Regulatory Compliance

Meet GDPR requirements and IVDR regulations.
All applications
designed with clinical-grade robustness

Creative &

Tech
Geniuses

To kick-start the development of Geeng, we have assembled a technical team of passionate problem-solvers capable of embodying our vision. This team ensures the creation of cutting-edge software solutions and builds the foundations for Geeng’s success. Together, we turn ambitious ideas into reality, one line of code at a time.

Everything you need to know 
before getting started.

  • What is DIAGNOW for biology decision making?

    DIAGNOW is a cloud-based or on-premise software solution designed for analysis and interpretation of genomic and multiplex biological data (dPCR and NGS). It is dedicated to assist biologists in their daily practice. Designed to support a wide range of laboratory environments, it empowers teams in clinical diagnostics, as well as those in bioproduction and quality control, with robust data analysis and interpretation workflows providing high decision-support capabilities. For healthcare professionals it empowers diagnosis, patient monitoring (coming soon), clinical variant interpretation and therapeutic decision-making. It integrates advanced bioinformatics, AI-driven system expertise, and knowledge-based prioritization to accelerate precision medicine and biological workflows.

  • Does DIAGNOW support digital PCR (dPCR) data analysis and interpretation?

    Yes, DIAGNOW is fully compatible with digital PCR (dPCR) workflows. It enables secure import, visualization, and interpretation of dPCR data for applications such as rare mutation detection, methylation quantification and copy number variation analysis. Results can be integrated with other omics data or reported independently for high-sensitivity clinical or QC applications.

  • Is DIAGNOW compatible with NGS data formats like WES, WGS, and targeted panels?

    Yes, DIAGNOW will soon fully supports next-generation sequencing (NGS) data including whole-genome sequencing (WGS), whole-exome sequencing (WES), targeted gene panels. It will allow SNV/INDELs, copy number variant (CNV), structural variants (SV) analysis but also additional biomarkers such as Microsatellite instability (MSI) and tumor mutational burden (TMB)... It will accept standard file formats such as VCF and tab-delimited files for streamlined processing. For end-to-end analysis, it is built to support pipelines starting from FASTQ and BAM files.

  • What are the benefits of choosing a cloud-based or on-premise deployment?

    Cloud deployment offers scalability, automatic updates, and global access, ideal for distributed teams. On-premise installation ensures maximum control over sensitive data, compliance with internal IT policies, and integration with secure hospital or laboratory infrastructure. However, it requires internal IT resources for deployment, maintenance, and system updates.

  • Can the platform integrate with LIMS or hospital EMR systems?

    Yes, DIAGNOW features a robust API that allows seamless integration with Laboratory Information Management Systems (LIMS), Electronic Medical Records (EMRs), and other healthcare IT platforms to ensure automated workflows and data consistency across systems.

  • Is the platform compliant with HIPAA, GDPR, ISO 27001, IVDR, and FDA 21 CFR Part 11 standards for medical data?

    Yes. Our platform is designed to comply with key international and European regulatory standards including HIPAA, GDPR, and FDA 21 CFR Part 11. We are actively pursuing full certification under the EU IVDR (In Vitro Diagnostic Regulation). For cloud deployments, we offer hosting on ISO 27001-certified and sovereign European cloud infrastructures that comply with EU data protection laws and France's HDS (Hébergement de Données de Santé) requirements for health data. Whether deployed in the cloud or on-premise, the platform guarantees secure data storage, encryption, access control, full audit trails, and compliance with both international and national standards for medical and health data processing.

  • Can clinical genomic reports be customized to fit laboratory branding and workflows?

    Yes, you can fully customize reports with your lab’s logo, templates, preferred terminology, and reporting style. The system also supports multilingual output and structured formats suitable for clinical records and patient communication.

  • What kind of training and support is available for clinical laboratories?

    We offer comprehensive onboarding, user training sessions, live technical support, and access to detailed documentation and video tutorials. Our customer success team ensures your lab is confident and effective from day one.

Unlock actionable 
insights from your genomic data.

Contact Us
2 biologists working and smiling on computer