Stereo-cell: Advancing spatial single-cell biology towards clinical translation
Christian Baumgartner
Clinical and Translational Medicine ›› 2025, Vol. 15 ›› Issue (9) : e70480
Stereo-cell: Advancing spatial single-cell biology towards clinical translation
Stereo-cell is a newly developed platform for spatial single-cell sequencing that integrates morphology, transcriptomics, and proteomics in high resolution. By preserving spatial context while enabling multimodal profiling, it bridges the gap between advanced omics and traditional pathology, supporting the detection of rare cells and clinically interpretable diagnoses. This letter highlights the technical innovations of Stereo-cell, its positioning within the spatial omics landscape, and its potential for precision medicine. Important challenges in data integration, regulatory compliance, and digital modelling are discussed as essential steps on the path to clinical implementation.
| [1] |
|
| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
|
| [9] |
|
| [10] |
|
| [11] |
|
| [12] |
|
| [13] |
|
| [14] |
|
| [15] |
International Organization for Standardization. ISO/IEC 27001: information security, cybersecurity and privacy protection. Geneva: ISO; 2018. Available from: https://www.iso.org/standard/27001 |
| [16] |
European Parliament and the Council of the European Union. Regulation (EU) 2017/746 of the European Parliament and of the Council on in vitro diagnostic medical devices (IVDR). Official Journal of the European Union. 2017. |
| [17] |
International Medical Device Regulators Forum (IMDRF). Software as a Medical Device (SaMD): Clinical Evaluation (IMDRF/SaMD WG/N41FINAL:2017). 2017. Available from: https://www.imdrf.org/documents/software-medical-device-samd-clinical-evaluation |
| [18] |
U.S. Food and Drug Administration (FDA), Health Canada, Medicines and Healthcare products Regulatory Agency (MHRA). Good machine learning practice for medical device development: guiding principles. 2021–2025. Available from: https://www.fda.gov/medical-devices/software-medical-device-samd/good-machine-learning-practice-medical-device-development-guiding-principles |
| [19] |
National Medical Products Administration (NMPA). Beijing: NMPA; [cited 2025 Aug 28]. Available from: https://english.nmpa.gov.cn |
2025 The Author(s). Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.
/
| 〈 |
|
〉 |