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

Laura Jiménez-GraciaDomenica MarcheseJuan C NietoGinevra CaratùElisa Melón-ArdanazVictoria GudiñoSara RothKellie WiseNatalie K RyanKirk B JensenXavier Hernando-MomblonaJoana P BernardesFlorian TranLaura Katharina SieversStefan SchreiberMaarten van den BergeTessa KolePetra L van der VeldeMartijn C NawijnPhilip RosenstielEduard BatlleLisa M ButlerIan A ParishJasmine PlummerIvo GutAzucena SalasHolger HeynLuciano G Martelotto
Published in: Genome biology (2024)
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.
Keyphrases
  • single cell
  • rna seq
  • high throughput
  • minimally invasive
  • endothelial cells
  • gene expression
  • magnetic resonance
  • image quality
  • induced pluripotent stem cells
  • solid state