FixNCut: single-cell genomics through reversible tissue fixation and dissociation

Laura Jiménez-Gracia(Centro Nacional de Análisis Genómico), Doménica Marchese(Centro Nacional de Análisis Genómico), Juan C. Nieto(Centro Nacional de Análisis Genómico), Ginevra Caratù(Centro Nacional de Análisis Genómico), Elisa Melón-Ardanaz(Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Victòria Gudiño(Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Sara Roth(The University of Melbourne), Kellie Wise(Australian Centre for Plant Functional Genomics), Natalie K. Ryan(South Australian Health and Medical Research Institute), Kirk B. Jensen(Australian Centre for Plant Functional Genomics), Xavier Hernando‐Momblona(Institute for Research in Biomedicine), Joana P. Bernardes(Christian-Albrechts-Universität zu Kiel), Florian Tran(Christian-Albrechts-Universität zu Kiel), Laura Katharina Sievers(Christian-Albrechts-Universität zu Kiel), Stefan Schreiber(Christian-Albrechts-Universität zu Kiel), Maarten van den Berge(University Medical Center Groningen), Tessa Kole(University Medical Center Groningen), Petra L. van der Velde(University Medical Center Groningen), Martijn C. Nawijn(University Medical Center Groningen), Philip Rosenstiel(Christian-Albrechts-Universität zu Kiel), Eduard Batlle(Institució Catalana de Recerca i Estudis Avançats), Lisa M. Butler(South Australian Health and Medical Research Institute), Ian A. Parish(The University of Melbourne), Jasmine Plummer(St. Jude Children's Research Hospital), Marta Gut(Centro Nacional de Análisis Genómico), Azucena Salas(Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Holger Heyn(Scope Group (United States)), Luciano G. Martelotto(Centre for Cancer Biology)
Genome biology
March 29, 2024
Cited by 14Open Access
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Abstract

The use of single-cell technologies for clinical applications requires disconnecting sampling from downstream processing steps. Early sample preservation can further increase robustness and reproducibility by avoiding artifacts introduced during specimen handling. We present FixNCut, a methodology for the reversible fixation of tissue followed by dissociation that overcomes current limitations. We applied FixNCut to human and mouse tissues to demonstrate the preservation of RNA integrity, sequencing library complexity, and cellular composition, while diminishing stress-related artifacts. Besides single-cell RNA sequencing, FixNCut is compatible with multiple single-cell and spatial technologies, making it a versatile tool for robust and flexible study designs.


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