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Cell type discovery using single-cell transcriptomics: Implications for ontological representation

  • Brian D. Aevermann
  • , Mark Novotny
  • , Trygve Bakken
  • , Jeremy A. Miller
  • , Alexander D. Diehl
  • , David Osumi-Sutherland
  • , Roger S. Lasken
  • , Ed S. Lein
  • , Richard H. Scheuermann
  • J. Craig Venter Institute
  • Allen Institute for Brain Science
  • Wellcome Trust
  • University of California at San Diego

Research output: Contribution to journalReview articlepeer-review

50 Scopus citations

Abstract

Cells are fundamental function units ofmulticellular organisms, with different cell types playing distinct physiological roles in the body. The recent advent of single-cell transcriptional profiling using RNA sequencing is producing 'big data', enabling the identification of novel human cell types at an unprecedented rate. In this review, we summarize recent work characterizing cell types in the human central nervous and immune systems using single-cell and single-nuclei RNA sequencing, and discuss the implications that these discoveries are having on the representation of cell types in the reference Cell Ontology (CL).We propose amethod, based on randomforestmachine learning, for identifying sets of necessary and sufficientmarker genes, which can be used to assemble consistent and reproducible cell type definitions for incorporation into the CL. The representation of defined cell type classes and their relationships in the CL using this strategy willmake the cell type classes being identified by high-throughput/high-content technologies findable, accessible, interoperable and reusable (FAIR), allowing the CL to serve as a reference knowledgebase of information about the role that distinct cellular phenotypes play in human health and disease.

Original languageEnglish
Pages (from-to)R40-R47
JournalHuman Molecular Genetics
Volume27
Issue numberR1
DOIs
StatePublished - May 1 2018

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