Single-Cell Sequencing

Single-cell RNA sequencing

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Instruments available

Available setups

Sample types

Bioinformatics expertise

What is single-cell RNA sequencing?

Single-cell RNA sequencing (scRNA-seq) enables the analysis of gene expression at the resolution of individual cells. This powerful technology allows researchers to uncover cellular heterogeneity, track cell lineage, and gain insight into complex tissue structures and dynamic biological processes.
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Instruments available

Single-cell RNA sequencing at OHMX.bio is performed using the AVITI platform in-house. For alternative approaches, partner access is maintained to the 10x Genomics Chromium system.

Available setups

OHMX.bio offers single-cell RNA sequencing using the PARSE scRNA-seq technology, a fixation-based method that enables sample storage for up to six months. This provides logistical flexibility, reduces batch effects, and eliminates the need for complex setups at the point of collection, such as in clinical environments. Multiple PARSE kit formats are supported, each tailored to distinct experimental designs and throughput requirements.

Sample types

A broad range of sample types is supported, including fresh and fixed tissues, dissociated tumor samples, cultured cells, and plant material. For full preparation and submission guidelines, see sample requirements page.

Advantages

  • High-throughput single-cell analysis
  • Sample fixation enables long-term storage and centralized processing
  • Reduced batch effects and improved reproducibility
  • No need for immediate onsite processing at clinical sites
  • Suitable for challenging or rare sample types

Common Applications

  • Tumor microenvironment characterization
  • Developmental biology
  • Plant tissue profiling
  • Immune cell profiling
  • Cell differentiation and lineage tracing

Integrated bioinformatics expertise

The experienced bioinformatics team at OHMX.bio works closely with scientists to analyze, visualize, and interpret single-cell data. Support includes clustering, differential expression analysis, cell-type annotation, and trajectory inference, ensuring that each dataset is transformed into clear, biologically meaningful results that support decision-making and downstream research translation.
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Partner with OHMX.bio

Whether you are conducting fundamental research, developing novel therapeutics, or advancing clinical diagnostics, OHMX.bio’s lab- and bio-IT solutions are here to support your goals. Our commitment to innovation, quality, and client success makes us the ideal partner for generating advanced biological insights.
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Let’s get in touch!

Are you curious about how we can work on your -omics challenges together? Fill out the form below!
Our experts will reply within 2 working days to freely discuss your omics project.

Our publications using single-cell RNA sequencing solutions

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