

EMEA | Summer 2026 Edition
Welcome to The Readout! Each quarter, we share a selection of highlights, updates, and resources for innovative investigators like you. Let’s jump right in — and happy reading.
A recent AbbVie study shows that Chromium Fixed RNA Profiling can generate meaningful single cell transcriptomic data from FFPE tissue, including colon, ileum, and skin samples. The workflow recovered diverse cell types, including challenging populations such as neutrophils and adipocytes, and showed good agreement with H&E imaging and fresh scRNA-seq reference data. These results support FFPE-compatible single cell workflows as a practical tool for retrospective clinical research.
Liu X, Naughton K, Karsen SD, Bentley P, Duggan L, Chaudhary N, Smith KM, Phillips L, Chang D, Mahi NA. Probing the Feasibility of Single-Cell Fixed RNA Sequencing from FFPE Tissue. International Journal of Molecular Sciences. 2026;27(3). 10.3390/ijms27031605
A new Nature Communications study introduces Spatial Perturb-Seq, an in vivo CRISPR screening approach that captures gene perturbation effects at single cell resolution within intact tissue. Using mouse brain, the authors showed how perturbations affect both targeted cells and neighboring cells, and demonstrated compatibility with Xenium for probe-based spatial analysis.
Shen K, Seow WY, Keng CT, Lim MGL, Lim DS, Guo K, Meliani A, Bin Hajis MI, Wang B, Prabhakar S, Chen KH, Chew WL. Spatial perturb-seq: single-cell functional genomics within intact tissue architecture. Nature Communications. 2026;17:3018. 10.1038/s41467-026-69677-6
We're pleased to share the winners of the EMEA Chromium Flex Apex Grant Program 2026. We were impressed by the range of proposals submitted from across the EMEA region, covering infectious disease, immunopathology, neuroscience, and hematology, with many researchers making excellent use of rare archival and fixed samples. Meet the winners:
We also want to spotlight EMEA-based winners of a recently concluded global 10x Genomics Single Cell Blood Analysis Grant Program. Congratulations to:
We’re excited to share that Proteintech Genomics is now part of the 10x Genomics family, bringing together two organizations with a shared commitment to advancing biological discovery. Read the full announcement here.
We are committed to ensuring continuity throughout this transition and supporting your research without disruption. and have created a dedicated page for support and technical documentation. Visit our Resources and customer support page.
Easy collection. Single cell resolution. Impactful results.
When blood samples and single cell analysis meet, researchers have access to an incredible source of actionable insights. The resulting data can drive the discovery of novel biomarkers, investigations into disease progression, and more accurate views of drug mechanisms of action.

With our latest protocols, blood samples can be collected and processed on a schedule that fits your project needs:
Resources now available
We're expanding automation support to help you scale your workflows with less manual effort:
Interested in automating your workflow? Have a look at our dedicated single cell automation page and reach out to your 10x Genomics representative to learn more.
Did you know that all our webinars are available to watch on-demand? Watch our latest webinar recording, and scroll down to register for what's upcoming.
As Flex expands to support more sample types and species, we're revisiting this earlier story on using GEM-X assays with challenging cardiovascular research samples.
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Uncover molecular insights, dissect cell-type differences, detect novel subtypes and biomarkers, decipher spatial gene expression patterns, and more... Get in touch to explore the possibilities for your research.
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