GAIA ClinicalTM

Unlock the potential of Clinical Metagenomics Data

overview

What You'll Get

GAIA CLINICALTM is a cloud-based solution leveraging proprietary algorithms for accurate pathogen detection from human samples.

Coverage & Confidence Metrics

Sequentia Biotech’s dual-algorithm workflow ensures reliable microbial identification by assessing both genome coverage and read distribution.

Pathogen reporting

Accurately detect and report the presence of pathogens down to the species level (depending on NGS method).

Presence of AMR markers reporting

Detection and reporting of antimicrobial resistance (AMR) genes present in the dataset, helping to assess the potential for antimicrobial resistance.

WORKFLOW

How it works

Complex bioinformatics, made simple. In just a few clicks, your analysis runs automatically and your results are ready to explore and download.

1.Upload your samples

Easily upload and centralize large datasets in a single, organized file manager.

2.Analyze your data in real time

Execute analyses automatically with live status tracking.

3.Visualize and explore your results

Navigate and interpret results through advanced visualization tools.

4.Download & share the results

Export results or share secure access with collaborators.

Publications

GAIA CLINICALTM featured in scientific research and publications as the metagenomics data analysis tool

Everything you need, unified in one platform with Sequentia Hub

GAIA CLINICALTM is powered by Sequentia Hub, a connected ecosystem of bioinformatics solutions. One platform, flexible access to all solutions.

designed to meet your needs

Ready to enhance your analysis with GAIA CLINICALTM?

Reproducibility

Ensure results reproducibility with stable validated algorithms.

Intuitive and user-friendly

No bioinformatics knowledge required.

Customer support

Access expert assistance when you need it.

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.

For research use only

This product is For Research Use Only (RUO). Not for use in diagnostic procedures.