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TCR Sequence Determination by TraCeR

TCR Sequencing

Michael Stubbington, Tapio Lonnberg and Sarah Teichmann
Sarah Teichmann, EMBL-EBI and the Wellcome Trust Sanger Institute, Cambridge, UK
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(...) Published on Rev A

  • supported ifcs:
    mRNA Seq IFC
  • number of ifc runs:
    5

Overview

This protocol is intended to produce data from T lymphocytes compatible with T cell receptor (TCR) sequence determination using the TraCeR computational method, as well as standard gene expression analysis. (See the Additional Documents section to download the TraCeR application note.) The single-cell cDNA is generated with the C1 Single-Cell mRNA Seq Protocol (PN 100 7168). The TCR sequence data is obtained from the sequenced samples using the TraCeR analysis pipeline and can be applied to both human and mouse datasets. The single-cell TCR sequences can then be associated with the single-cell gene expression data for combined clonotype and phenotype information with single-cell resolution.

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Protocol: TCR Sequence Determination by TraCeRDuration (H:M): 10:00

Cell Load and Stain

Sample Prep

view protocol worksheet

Tested Primary Cells or Cell Lines

Cell Name Cell Type Source
Mouse splenic CD4+ effector and memory T lymphocytes Primary mouse splenocytes Primary

Performance

To demonstrate and validate our method for TCR sequence reconstruction we analyzed single cell mRNA sequencing data from 272 flow-sorted CD4+ T cells isolated from spleens of C57BL/6 mice. The samples were sequenced on an Illumina HiSeq 2500 System sequencer using paired-end 100 bp reads. We were able to detect at least one productive alpha chain in 74-96% of cells, a productive beta chain in 88-96% of cells, and paired productive alpha/beta chains in 70-93% of cells. An assessment of the sensitivity with varying read depth and read length can be found in Stubbington, M.J., Lonnberg, T., Proserpio, V. et al. "T cell fate and clonality inference from single-cell transcriptomes." Nature Methods 13 (2016): 329-32. For qPCR orthogonal validation we took 185 cells for which we had RNA seq data and used full-length SMART-Seq-derived cDNA as template material in PCR reactions. We designed the PCR to amplify a region from within the V gene up to the constant segment. In total, 485 recombinant sequences were identified by qPCR, mRNA seq, or both approaches, of which 371 (76.5%) were concordant. A full discussion of the orthogonal validation is available in the Supplemental Materials of Stubbington, M.J. et al. Nature Methods 13 (2016): 329-32.

Publications or Articles

Performance data

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Additional documents

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