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RHEO In Action: A Snapshot of Innovation
Discover how users can effortlessly automate complex bioinformatics analyses with RHEO's push-button solution, designed to handle any use case or data modality. With seamless integration into existing external systems like cloud storage buckets, local databases, and LIMS systems, RHEO accelerates the pace of discovery, leading to faster, more profound insights into your data.
Expanding Your Research Horizons: Single Cell and Spatial Transcriptomics Capabilities in Biomedical Research
Discover how single-cell RNA sequencing and spatial transcriptomics are transforming our understanding of tissue cell diversity, developmental processes, and tumor heterogeneity.
Accelerating Drug Discovery: How GRAF Pangenomes Enable Enhanced Insights From Sequencing Data.
Uncover solutions to the pressing challenges in Next-Generation Sequencing (NGS) data analysis with Velsera. Join our upcoming webinar to address a pivotal pain point in genomics: reference bias. Learn how Velsera's GRAF solution tackles reference bias and seamlessly integrates with existing pipelines, lowering computational costs and elevating your NGS analysis efficiency.
RHEO In Action: A Snapshot of Innovation
Discover how users can effortlessly automate complex bioinformatics analyses with RHEO's push-button solution, designed to handle any use case or data modality. With seamless integration into existing external systems like cloud storage buckets, local databases, and LIMS systems, RHEO accelerates the pace of discovery, leading to faster, more profound insights into your data.
Expanding Your Research Horizons: Single Cell and Spatial Transcriptomics Capabilities in Biomedical Research
Discover how single-cell RNA sequencing and spatial transcriptomics are transforming our understanding of tissue cell diversity, developmental processes, and tumor heterogeneity.
Accelerating Drug Discovery: How GRAF Pangenomes Enable Enhanced Insights From Sequencing Data.
Uncover solutions to the pressing challenges in Next-Generation Sequencing (NGS) data analysis with Velsera. Join our upcoming webinar to address a pivotal pain point in genomics: reference bias. Learn how Velsera's GRAF solution tackles reference bias and seamlessly integrates with existing pipelines, lowering computational costs and elevating your NGS analysis efficiency.
Ask what’s possible with Velsera.
