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 setting up software and servers, and not enough time on the science itself.
Upload your data through a secure link and run it with ready-to-use, validated workflows. Nothing to install or maintain, and no technical skills needed.
Every workflow uses trusted, widely-used open-source tools backed by published research. We manage technical configuration for you.
Whether you’re analysing one sample or hundreds, our cloud infrastructure scales automatically to match computing needs.
Every analysis gives you an interactive report and downloadable files, ready to review, reuse, or plug into your own pipeline.
| Building it yourself | With Genomix Cloud |
|---|---|
| Install dependencies | Upload FASTQ |
| Configure tools | Run validated workflow |
| Manage databases | Review report |
| Write scripts | Download results |
| Troubleshoot failures | |
| Maintain versions | |
| Manage compute |
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 through a secure link. 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.
Join the early users exploring a new way to run bioinformatics pipelines. Sign up for a free trial — no credit card required.