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The spatial RNA integrity number assay for in situ evaluation of transcriptome quality.

Linda KvastadKonstantin CarlbergLudvig LarssonEva Gracia VillacampaAlexander StuckeyLinnea StenbeckAnnelie MollbrinkMargherita ZamboniJens Peter MagnussonElisa BasmaciAlia ShamikhGabriela ProchazkaAnna-Lena SchauppÅke BorgLars FuggerMonica NistérJoakim Lundeberg
Published in: Communications biology (2021)
The RNA integrity number (RIN) is a frequently used quality metric to assess the completeness of rRNA, as a proxy for the corresponding mRNA in a tissue. Current methods operate at bulk resolution and provide a single average estimate for the whole sample. Spatial transcriptomics technologies have emerged and shown their value by placing gene expression into a tissue context, resulting in transcriptional information from all tissue regions. Thus, the ability to estimate RNA quality in situ has become of utmost importance to overcome the limitation with a bulk rRNA measurement. Here we show a new tool, the spatial RNA integrity number (sRIN) assay, to assess the rRNA completeness in a tissue wide manner at cellular resolution. We demonstrate the use of sRIN to identify spatial variation in tissue quality prior to more comprehensive spatial transcriptomics workflows.
Keyphrases
  • gene expression
  • single cell
  • quality improvement
  • high throughput
  • nucleic acid
  • heat stress
  • heat shock protein