Author
Listed:
- Yixing Dong
(Lausanne University Hospital; University of Lausanne)
- Chiara Saglietti
(Lausanne University Hospital and University of Lausanne)
- Quentin Bayard
(Owkin)
- Almudena Espin Perez
(Owkin)
- Sabrina Carpentier
(Owkin)
- Daria Buszta
(Lausanne University Hospital; Swiss Cancer Center Leman)
- Stephanie Tissot
(Lausanne University Hospital; Swiss Cancer Center Leman
Ludwig Insitute for Cancer Research)
- Rémy Dubois
(Owkin)
- Atanas Kamburov
(Owkin)
- Senbai Kang
(Lausanne University Hospital; University of Lausanne)
- Carla Haignere
(Owkin)
- Rita Sarkis
(Lausanne University Hospital and University of Lausanne)
- Sylvie Andre
(Lausanne University Hospital; Swiss Cancer Center Leman
Ludwig Insitute for Cancer Research
Agora Translational Research Center)
- Marina Alexandre Gaveta
(Lausanne University Hospital; Swiss Cancer Center Leman
Ludwig Insitute for Cancer Research
Agora Translational Research Center)
- Silvia Lopez Lastra
(Owkin)
- Nathalie Piazzon
(Lausanne University Hospital and University of Lausanne)
- Rita Santos
(Owkin)
- Katharina Loga
(Owkin)
- Caroline Hoffmann
(Owkin)
- George Coukos
(Lausanne University Hospital; Swiss Cancer Center Leman
Ludwig Insitute for Cancer Research
Agora Translational Research Center)
- Solange Peters
(Lausanne University Hospital; Swiss Cancer Center Leman)
- Vassili Soumelis
(Owkin)
- Eric Yves Durand
(Owkin)
- Laurence Leval
(Lausanne University Hospital and University of Lausanne)
- Raphael Gottardo
(Lausanne University Hospital; University of Lausanne
Agora Translational Research Center
Swiss Institute of Bioinformatics
Ecole Polytechnique Fédérale de)
- Krisztian Homicsko
(Lausanne University Hospital; Swiss Cancer Center Leman
Ludwig Insitute for Cancer Research
Agora Translational Research Center)
- Elo Madissoon
(Owkin)
Abstract
Recent advancements in probe-based, full-transcriptome technologies for FFPE tissues, such as Visium CytAssist, Chromium Flex, and GeoMx DSP, enable analysis of archival samples, facilitating the generation of data from extensive cohorts. However, these methods can be labor-intensive and costly, requiring informed selection based on research objectives. We compare these methods on FFPE tumor samples in Breast, NSCLC and DLBCL showing 1) good-quality, highly reproducible data from all methods; 2) GeoMx data containing cell mixtures despite marker-based preselection; 3) Visium and Chromium outperform GeoMx in discovering tumor heterogeneity and potential drug targets. We recommend the use of Visium and Chromium for high-throughput and discovery projects, while the manually more challenging GeoMx platform with targeted regions remains valuable for specialized questions.
Suggested Citation
Yixing Dong & Chiara Saglietti & Quentin Bayard & Almudena Espin Perez & Sabrina Carpentier & Daria Buszta & Stephanie Tissot & Rémy Dubois & Atanas Kamburov & Senbai Kang & Carla Haignere & Rita Sark, 2025.
"Transcriptome analysis of archived tumors by Visium, GeoMx DSP, and Chromium reveals patient heterogeneity,"
Nature Communications, Nature, vol. 16(1), pages 1-18, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59005-9
DOI: 10.1038/s41467-025-59005-9
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