Abstract

New high-dimensional, single-cell technologies offer unprecedented resolution in the analysis of heterogeneous tissues. However, because these technologies can measure dozens of parameters simultaneously in individual cells, data interpretation can be challenging. Here we present viSNE, a tool that allows one to map high-dimensional cytometry data onto two dimensions, yet conserve the high-dimensional structure of the data. viSNE plots individual cells in a visual similar to a scatter plot, while using all pairwise distances in high dimension to determine each cell's location in the plot. We integrated mass cytometry with viSNE to map healthy and cancerous bone marrow samples. Healthy bone marrow automatically maps into a consistent shape, whereas leukemia samples map into malformed shapes that are distinct from healthy bone marrow and from each other. We also use viSNE and mass cytometry to compare leukemia diagnosis and relapse samples, and to identify a rare leukemia population reminiscent of minimal residual disease. viSNE can be applied to any multi-dimensional single-cell technology.

Keywords

Genetic heterogeneityPhenotypeVisualizationComputational biologySingle-cell analysisSpatial heterogeneityBiologyLeukemiaCellGeneticsComputer scienceData miningGeneEcology

MeSH Terms

BiomarkersTumorBone Marrow NeoplasmsCell LineageHumansImage CytometryImmunophenotypingLeukemiaNeoplasm RecurrenceLocalRecurrenceSingle-Cell Analysis

Affiliated Institutions

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Publication Info

Year
2013
Type
article
Volume
31
Issue
6
Pages
545-552
Citations
1603
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

1603
OpenAlex
58
Influential
1462
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Cite This

El-ad David Amir, Kara L. Davis, Michelle D. Tadmor et al. (2013). viSNE enables visualization of high dimensional single-cell data and reveals phenotypic heterogeneity of leukemia. Nature Biotechnology , 31 (6) , 545-552. https://doi.org/10.1038/nbt.2594

Identifiers

DOI
10.1038/nbt.2594
PMID
23685480
PMCID
PMC4076922

Data Quality

Data completeness: 86%