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      COMPREHENSIVE CLASSIFICATION OF RETINAL BIPOLAR NEURONS BY SINGLE-CELL TRANSCRIPTOMICS

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          SUMMARY

          Patterns of gene expression can be used to characterize and classify neuronal types. It is challenging, however, to generate taxonomies that fulfill the essential criteria of being comprehensive, harmonizing with conventional classification schemes, and lacking superfluous subdivisions of genuine types. To address these challenges, we used massively parallel single-cell RNA profiling and optimized computational methods on a heterogeneous class of neurons, mouse retinal bipolar cells (BCs). From a population of ~25,000 BCs we derived a molecular classification that identified 15 types including all types observed previously, and two novel types, one of which has a non-canonical morphology and position. We validated the classification scheme and identified dozens of novel markers using methods that match molecular expression to cell morphology. This work provides a systematic methodology for achieving comprehensive molecular classification of neurons, identifies novel neuronal types, and uncovers transcriptional differences that distinguish types within a class.

          eTOC

          Single-cell transcriptome sequencing of retinal bipolar cells reveals known and new types including one with a non-canonical morphology.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          3 August 2016
          25 August 2016
          25 August 2017
          : 166
          : 5
          : 1308-1323.e30
          Affiliations
          [1 ]Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA
          [2 ]Department of Genetics, Harvard Medical School, Boston, MA 02115, USA
          [3 ]Department of Ophthalmology, Harvard Medical School, Boston, MA 02115, USA
          [4 ]Center for Brain Science and Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02130, USA
          [5 ]Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA
          [6 ]Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA
          [7 ]Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA
          [8 ]Department of Biology and Koch Institute, MIT, Cambridge, MA 02139, USA
          Author notes
          Article
          PMC5003425 PMC5003425 5003425 nihpa807574
          10.1016/j.cell.2016.07.054
          5003425
          27565351
          dad49d95-8067-42ca-abeb-406927b8135c
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