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A single-cell and single-nucleus RNA-Seq toolbox for fresh and frozen human tumors.

Michal SlyperCaroline B M PorterOrr AshenbergJulia WaldmanEugene DrokhlyanskyIsaac WakiroChristopher SmillieGabriela Smith-RosarioJingyi WuDanielle DionneSébastien VigneauJudit Jané-ValbuenaTimothy L TickleSara NapolitanoMei-Ju SuAnand G PatelAsa KarlstromSimon GritschMasashi NomuraAvinash WaghraySatyen H GohilAlexander M TsankovLivnat Jerby-ArnonOfir CohenJohanna KlughammerYanay RosenJoshua GouldLan NguyenMatan HofreePeter J TramontozziBo LiCatherine J WuBenjamin IzarRizwan HaqF Stephen HodiCharles H YoonAaron N HataSuzanne J BakerMario L SuvàRaphael BuenoElizabeth H StoverMichael R ClayMichael A DyerNatalie B CollinsUrsula A MatulonisNikhil WagleBruce E JohnsonAsaf RotemOrit Rozenblatt-RosenAviv Regev
Published in: Nature medicine (2020)
Single-cell genomics is essential to chart tumor ecosystems. Although single-cell RNA-Seq (scRNA-Seq) profiles RNA from cells dissociated from fresh tumors, single-nucleus RNA-Seq (snRNA-Seq) is needed to profile frozen or hard-to-dissociate tumors. Each requires customization to different tissue and tumor types, posing a barrier to adoption. Here, we have developed a systematic toolbox for profiling fresh and frozen clinical tumor samples using scRNA-Seq and snRNA-Seq, respectively. We analyzed 216,490 cells and nuclei from 40 samples across 23 specimens spanning eight tumor types of varying tissue and sample characteristics. We evaluated protocols by cell and nucleus quality, recovery rate and cellular composition. scRNA-Seq and snRNA-Seq from matched samples recovered the same cell types, but at different proportions. Our work provides guidance for studies in a broad range of tumors, including criteria for testing and selecting methods from the toolbox for other tumors, thus paving the way for charting tumor atlases.
Keyphrases
  • single cell
  • rna seq
  • high throughput
  • induced apoptosis
  • endothelial cells
  • cell cycle arrest
  • cell death
  • mesenchymal stem cells
  • dna methylation
  • quality improvement
  • signaling pathway
  • electronic health record