Analyse sequencing data using validated bioinformatics workflows without installing multiple bioinformatics tools
and leverage secure, scalable cloud computing to run analyses efficiently.
Select an analysis, upload your sequencing data, run the pipeline in the cloud, and download your results from anywhere using only an internet connection.
Research teams spend too much time installing and configuring tools, provisioning compute resources, and executing repetable analysis workflows instead of focusing on genomic insights.
Upload your sequencing data through your web browser and run it using validated bioinformatics workflows. There is no software to install, configure, or maintain. Analyses are pre-built and ready to use without the need of techical skills.
Every workflow is built using widely adopted open-source bioinformatics tools that are described in reviewed publications. Tool versions and configuration are managed and fully citable.
Whether you are analysing a single sample or hundreds, our AWS infraestructure provides cloud computing resources scale automatically to match your analysis computer needs. There is no infrastructure to manage.
Every analysis generates interactive reports and downloadable output files, enabling researchers to review results, perform downstream analyses, and integrate findings into their existing research workflows.
One platform, five steps. Follow a transparent workflow from your initial upload to downloadable results for downstream research.
Validated, open-source workflows pre-configured by bioinformatics specialists.
Upload FASTQ files directly. No local installation or scripting required.
Processed on AWS infrastructure, encrypted in transit and at rest.
Structured, explorable results — built for scrutiny, not just presentation.
CSV tables and output files, ready for downstream analysis or publication.
Genomix Cloud supports both ready-to-use analyses and custom pipeline integration, enabling research teams to run the workflows they need without managing complex infrastructure. All analyses are intended for Research Use Only.
Start with validated workflows developed and tested for reliable genomic analysis.
Identify and compare bacterial and viral genomes, uncovering variations, insights, and functional annotations.
These pipelines are planned for future development, prioritised based on research needs.
Taxonomic profiling, functional annotation, and diversity analysis for complex microbial communities.
RoadmapSomatic variant calling, copy number analysis, and mutational signature extraction from tumour sequencing.
RoadmapStatistical parentage testing using 2bRAD-Seq with probabilistic genotyping-by-sequencing for forensic applications.
RoadmapRNA-Seq alignment, differential expression analysis, assembly, and single-cell RNA workflows.
RoadmapDon’t see the analysis you need? Work with our team to integrate your existing pipeline
or develop support for a new workflow tailored to your research requirements.
“Every research team has different analytical needs. We built Genomix Cloud to provide a flexible foundation for genomic analysis—combining validated workflows with the ability to integrate new pipelines and adapt to evolving research requirements.”
Genomix Cloud Team
Join the early users exploring a new way to run bioinformatics pipelines. Sign up for a free trial — no credit card required.