Evidence map›Paper›PMID 26274018›Full record

ArticleCytometry. Part A : the journal of the International Society for Analytical Cytology2016

Mapping cell populations in flow cytometry data for cross-sample comparison using the Friedman-Rafsky test statistic as a distance measure.

Chiaowen Hsiao, Mengya Liu, Rick Stanton, Monnie McGee, Yu Qian, Richard H Scheuermann

Abstract read
In one paragraph

Article in Cytometry. Part A : the journal of the International Society for Analytical Cytology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Predicting Cell Populations in Single Cell Mass Cytometry Data.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Chiaowen HsiaoCenter for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland.
Mengya LiuDepartment of Statistical Science, Southern Methodist University, Dallas, Texas.
Rick StantonDepartment of Informatics, J. Craig Venter Institute, La Jolla, California.
Monnie McGeeDepartment of Statistical Science, Southern Methodist University, Dallas, Texas.
Yu QianDepartment of Informatics, J. Craig Venter Institute, La Jolla, California.
Richard H ScheuermannDepartment of Informatics, J. Craig Venter Institute, La Jolla, California.

Funding

Bioinformatics Approach to Influenza A/H1N1 Vaccine Immune ProfilingU01AI089859 · NIAID · MAYO CLINIC ROCHESTER · PI POLAND, GREGORY A. · 2010 to 2015
$33.8M
The Statistical and Computational Analysis of Flow Cytometry DataR01EB008400 · NIBIB · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GOTTARDO, RAPHAEL · 2008 to 2015
$2.9M
NIAID NIH HHS U01AI089859NIBIB NIH HHS R01EB008400PHS HHS HHSN272201200005C
6 · The paper itself

Abstract

Flow cytometry (FCM) is a fluorescence-based single-cell experimental technology that is routinely applied in biomedical research for identifying cellular biomarkers of normal physiological responses and abnormal disease states. While many computational methods have been developed that focus on identifying cell populations in individual FCM samples, very few have addressed how the identified cell populations can be matched across samples for comparative analysis. This article presents FlowMap-FR, a novel method for cell population mapping across FCM samples. FlowMap-FR is based on the Friedman-Rafsky nonparametric test statistic (FR statistic), which quantifies the equivalence of multivariate distributions. As applied to FCM data by FlowMap-FR, the FR statistic objectively quantifies the similarity between cell populations based on the shapes, sizes, and positions of fluorescence data distributions in the multidimensional feature space. To test and evaluate the performance of FlowMap-FR, we simulated the kinds of biological and technical sample variations that are commonly observed in FCM data. The results show that FlowMap-FR is able to effectively identify equivalent cell populations between samples under scenarios of proportion differences and modest position shifts. As a statistical test, FlowMap-FR can be used to determine whether the expression of a cellular marker is statistically different between two cell populations, suggesting candidates for new cellular phenotypes by providing an objective statistical measure. In addition, FlowMap-FR can indicate situations in which inappropriate splitting or merging of cell populations has occurred during gating procedures. We compared the FR statistic with the symmetric version of Kullback-Leibler divergence measure used in a previous population matching method with both simulated and real data. The FR statistic outperforms the symmetric version of KL-distance in distinguishing equivalent from nonequivalent cell populations. FlowMap-FR was also employed as a distance metric to match cell populations delineated by manual gating across 30 FCM samples from a benchmark FlowCAP data set. An F-measure of 0.88 was obtained, indicating high precision and recall of the FR-based population matching results. FlowMap-FR has been implemented as a standalone R/Bioconductor package so that it can be easily incorporated into current FCM data analytical workflows.

Indexed as

Adaptor Proteins, Signal TransducingAlgorithmsBiomarkersCD4 AntigensComputational BiologyData Interpretation, StatisticalFlow CytometryHumansLeukocyte Common AntigensPhosphoproteinsZAP-70 Protein-Tyrosine KinaseAdaptor Proteins, Signal TransducingBiomarkersCD4 AntigensLeukocyte Common AntigensPhosphoproteinsSLP-76 signal Transducing adaptor proteinsZAP70 protein, humanZAP-70 Protein-Tyrosine Kinasecell population matchingcross-sample comparisonflow cytometryFriedman-Rafsky testminimum spanning treesingle-cell analysis

Identifiers

PMID26274018
PMCPMC5014134

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.