Single cell RNA-seq

Dissect heterogeneity at the single-cell level. Use flexible preprocessing workflows in Pluto scRNA-seq and analyze individual cell gene expression profiles, uncovering cellular diversity and function by cell type, condition. Single-cell RNA sequencing (scRNA-seq) is a powerful technique for examining the gene expression of individual cells, providing unprecedented insights into cellular diversity and function within complex biological systems. By analyzing gene expression at the single-cell level, researchers can identify novel cell types and states, track developmental processes, and understand mechanisms of disease progression. Pluto Bio's platform streamlines scRNA-seq data analysis, offering scalable, secure, and user-friendly tools for transformative biological insights.

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Unlocking cellular complexity with Pluto

Pluto simplifies the complexity of scRNA-seq data analysis. Our platform provides an integrated solution for processing, analyzing, and visualizing single-cell data. From identifying cell types to uncovering gene expression patterns, Pluto empowers researchers to gain deep insights into the cellular mechanisms driving biological processes and disease states.

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Empower your research with cutting-edge analytics

Pluto's advanced analytics engine enables researchers to seamlessly navigate the intricacies of single-cell data. Leverage our intuitive tools to perform differential expression analysis, cluster identification, and trajectory inference, all within a collaborative and secure cloud environment.

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Accessible single-cell genomics

With Pluto, accessing the power of scRNA-seq analysis doesn't require computational expertise. Our user-friendly platform breaks down barriers, allowing scientists from diverse backgrounds to explore the cellular landscape, drive discovery, and accelerate innovation in genomics research.

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Why scRNA-seq?

High-resolution insights

  • Single-cell level analysis
  • Uncover cellular heterogeneity and rare cell populations

Streamlined data integration

  • Harmonize scRNA-seq data with other omics data
  • Facilitate comprehensive multi-omics analyses

Advanced analytical tools

  • Pre-built and custom pipelines
  • Easy-to-use interfaces for complex analyses
  • No coding skills required for advanced data interpretation