The Platform for Scalable Genomics
Manage, validate, and scale omics research with Seqera—the platform built for the scientific data lifecycle. Designed for bioinformatics, trusted by enterprises.
Request a DemoAccelerate Genomics with Scalable Bioinformatics
Genomics research is generating unprecedented volumes of data, from whole genome sequencing to single-cell transcriptomics. To keep pace, bioinformaticians need powerful, scalable tools for efficient and reproducible data analysis. Built for enterprise-scale, Seqera is the comprehensive platform for collaborative, end-to-end omics analysis—accelerating the path from raw data to real-world impact.
RNA sequencing analysis
Chromatin accessibility profiling
Viral genome assembly
Amplicon sequencing
Differential abundance analysis
DNA methylation analysis
ChIP-seq peak calling
Metagenome assembly
Why Seqera for Genomics?
Seqera enables organizations to operationalize genomics at scale, accelerating analysis, improving reproducibility, and reducing infrastructure complexity. From sequencing to interactive insights, Seqera provides the enterprise-grade foundation to deploy, manage, and scale high-throughput bioinformatics across research, translational, and clinical domains.
Effortless Genomic Scaling
Dynamically scale analysis capacity with seamless access to your data, cloud, and compute—without infrastructure limitations or vendor lock-in. Built to scale from proof-of-concept to global R&D.
Deploy Genomics Anywhere
Run large-scale genomics workloads on any cloud, on-premises, or hybrid environment with flexible deployment options that meet your IT and regulatory needs.
Seamless Collaboration
Break down silos across global teams and partners with real-time collaboration and secure sharing of data, analyses, and results, enabling rapid cross-validation of findings and faster decision-making.
Reproducibility Without Compromise
Leverage Nextflow and nf-core to automate and standardize genomics analyses, ensuring full traceability, consistency, and reproducibility from development to production.
From the Creators of Nextflow
Receive expert support directly from the team behind Nextflow, with professional bioinformaticians guiding you through onboarding, optimization, and long-term innovation.
Enterprise-Grade Security & Compliance
Integrate seamlessly with your infrastructure while meeting enterprise security, compliance, and data governance needs and ensuring sustainability for future growth.
How Seqera is Powering Genomics
Seqera centralizes data, code, computing, and environments, giving scientists seamless access to best-practice pipelines from organizations including nf-core, Sanger, and other top institutions on a single, scalable platform. By automating and optimizing workflows, Seqera reduces infrastructure challenges, lowers costs, and accelerates large-scale genomic analysis.
Launch Analysis in One Click
Get started instantly with trusted, open-source Nextflow pipelines from the nf-core community, or bring your own.
Discover Real-World Applications
Explore applications of Nextflow and Seqera in omics research with these useful resources.
Trusted by 150+ Leading Organizations
Pharma and biotech companies, academia, and national sequencing initiatives rely on Nextflow and Seqera to power their genomics research. From Biopharma R&D and Clinical Diagnostics, to large-scale consortia projects to precision medicine studies, Seqera delivers the computational backbone for groundbreaking discoveries.
Clinical Diagnostics
"We have scaled our pathogen genomic surveillance capacity by 10 times"
Biotech
"We were able to scale single-cell genomics to deliver clinical impact at industry-leading costs"
Life Sciences R&D
"Seqera provided us with huge flexibility to deploy genomics workloads anywhere"
