Build, Validate & Scale Nextflow with Seqera
Whether you’re working in genomics, transcriptomics, or proteomics, Seqera helps bioinformaticians run Nextflow pipelines more efficiently. By removing the pain of managing dependencies and infrastructure, your analyses scale reproducibly on HPC, hybrid, or cloud. Book a demo and see why Seqera is trusted by bioinformaticians from pharma and diagnostics teams worldwide.
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Why Bioinformaticians & Data Scientists Choose Seqera
- Built and Supported by the Team Behind Nextflow Seqera was created by the original developers of Nextflow, making it the only platform purpose-built for the language. With direct access to its creators and maintainers, you benefit from deep expertise, best practices, and confidence that your workflows run on the stack designed for them.
- Reproducible Pipelines, Anywhere Run genomics, transcriptomics, and proteomics workflows consistently across HPC, hybrid, and cloud. Ensure results can be trusted and repeated every time, no matter the environment.
- Productivity At Every Stage Develop, test, and optimize pipelines faster with AI assistance and nf-core best practices. Spend less time on debugging and more time on scientific discovery.
- Improved Visibility and Collaboration Share pipelines, track resources, and troubleshoot jobs with unified metrics and logging. Teams work more efficiently with a single view of data, runs, and performance.
- Seamless Execution Ecosystem Use Wave, Fusion, and MultiQC to simplify container provisioning, data orchestration, and quality control. Automate the hard parts so you can focus on running analyses at scale.
Delivering Real-World Results
5x+
Reduction in pipeline run time
“We reduced pipeline runtime from 8 days to just 1.5 days, boosting efficiency and accelerating data analysis. This drastic reduction in TAT enabled our customer to increase processing from 1 batch/week to 20 batches/week, ensuring that the pipeline is not a bottleneck.”
— Senior Director, Strand Life Sciences
1000s
Of samples processed per day on the same compute
“In one project, 1000s of cells per patient were processed over just 2 weeks, enabling rapid return of results to help make faster, more informed decisions on the etiology of disease and treatment response.”
— VP Computational Biology & Analytics, BioSkryb Genomics
50%
Less time running workflows
“By running our Nextflow pipelines with Seqera, we now spend 50% less time compared to running individual workflows on EC2.”
— Associate Director of Data and Engineering, Sage Bionetworks
5x+
Reduction in pipeline run time
“We reduced pipeline runtime from 8 days to just 1.5 days, boosting efficiency and accelerating data analysis. This drastic reduction in TAT enabled our customer to increase processing from 1 batch/week to 20 batches/week, ensuring that the pipeline is not a bottleneck.”
— Senior Director, Strand Life Sciences
1000s
Of samples processed per day on the same compute
“In one project, 1000s of cells per patient were processed over just 2 weeks, enabling rapid return of results to help make faster, more informed decisions on the etiology of disease and treatment response.”
— VP Computational Biology & Analytics, BioSkryb Genomics
50%
Less time running workflows
“By running our Nextflow pipelines with Seqera, we now spend 50% less time compared to running individual workflows on EC2.”
— Associate Director of Data and Engineering, Sage Bionetworks
Equip your team with the platform purpose-built for bioinformaticians using Nextflow.
Book a demo today and see how Seqera can help your science scale securely and reproducibly.