Mytho develops customised NGS panels, advanced sequencing solutions and optimised bioinformatics pipelines to support clinical and research applications.
Mytho develops customised NGS panels, advanced sequencing solutions and optimised bioinformatics pipelines to support clinical and research applications.
Customised solutions in the most innovative field of molecular biology.
Mytho develops customised NGS panels, advanced sequencing solutions and optimised bioinformatics pipelines for clinical and research applications. We support diagnostic and R&D teams in the analysis of complex genomic data, enabling the generation of reliable insights, deeper interpretations and more efficient workflows.
Mytho offers NGS sequencing solutions and bioinformatics tools that enable laboratories and clinical teams to analyse complex genomic data in a personalised manner.
We support professionals with the design and supply of customised panels for the generation of reliable and interpretable insights.
Thanks to customised NGS panels and optimised pipelines, Mytho enables the detection of even low-frequency genomic variants, improving the depth and quality of analysis compared to standard workflows.
Automated bioinformatics processes reduce manual steps and accelerate the design of new panels.
The design of custom panels and the integration of standardised pipelines ensure consistency between different runs, reducing variability and facilitating the management of the sequencing process.
Our four NGS pillars
Custom NGS panels
Targeted genetic design and optimised coverage for specific targets.
Integrated bioinformatics
Modular pipelines, advanced annotations, and intelligent filters.
Flexibility
Models and algorithms for interpreting and adapting specific and unique requests.
Scalability & compatibility
Multi-platform support for laboratories and research teams.
Areas where Mytho brings real value
Molecular oncology
Analysis of driver mutations, genomic signatures, and targeted panels to support studies on therapeutic targets and monitoring of tumour variants.
Rare diseases
Highly specific NGS panels for complex gene sets and critical regions, with optimised pipelines to identify rare variants with high sensitivity.
Screening
Extended sequencing solutions for neonatal, paediatric or at-risk population screening for the early detection of risk conditions.
Precision medicine
Support for the integration of genomic data for the definition of biomarkers and predictive signatures useful for guiding therapeutic decisions and research protocols.
Compatible technologies and advanced bioinformatics
Compatible technologies and advanced bioinformatics
Modular pipelines
Flexible, adaptable processes designed to evolve.
Our pipelines combine independent modules to manage targeted NGS analysis, targeted sequencing, and complex workflows. The modular structure allows for precision, consistency, and continuous updating, minimising the impact on laboratory activities.
Cross-platform compatibility
A single architecture, infinite integrations.
Strong design, quality in synthesis.
Consistent uniformity, every session.
We utilise the best production processes and industrial partners for probe synthesis, ensuring uniformity and precision in every run and maximising depth in every flow cell.
Versioning & quality
Control, traceability and stability of the workflow.
Each pipeline is versioned and monitored to ensure reproducibility and consistent quality. Data governance ensures documented processes, verifiable parameters and secure management of information assets, which are essential for collaborative projects and long-term analysis.