Evidence map›Paper›PMID 26755197›Full record

ArticleBMC bioinformatics2016

BayesFlow: latent modeling of flow cytometry cell populations.

Kerstin Johnsson, Jonas Wallin, Magnus Fontes

Erratum issuedAbstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. A variational deep-learning approach to modeling memory T cell dynamics.bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Visualizing scRNA-Seq Data at Population Scale with GloScope.bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. A Bayesian feature allocation model for identifying cell subpopulations using CyTOF data.Journal of the Royal Statistical Society. Series C, Applied statistics · 2023
    Article
  11. Article
  12. Article
  13. Machine Learning of Discriminative Gate Locations for Clinical Diagnosis.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2020
    Article
  14. Article
  15. Article
  16. Review
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Kerstin JohnssonCentre for Mathematical Sciences, Lund University, Box 118, Lund, S-221 00, Sweden. johnsson@maths.lth.se.
Jonas WallinMathematical Sciences, Chalmers and University of Gothenburg, Gothenburg, S-412 58, Sweden. jonwal@chalmers.se.
Magnus FontesCentre for Mathematical Sciences, Lund University, Box 118, Lund, S-221 00, Sweden. fontes@maths.lth.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFlow cytometry is a widespread single-cell measurement technology with a multitude of clinical and research applications. Interpretation of flow cytometry data is hard; the instrumentation is delicate and can not render absolute measurements, hence samples can only be interpreted in relation to each other while at the same time comparisons are confounded by inter-sample variation. Despite this, most automated flow cytometry data analysis methods either treat samples individually or ignore the variation by for example pooling the data. A key requirement for models that include multiple samples is the ability to visualize and assess inferred variation, since what could be technical variation in one setting would be different phenotypes in another.

resultsWe introduce BayesFlow, a pipeline for latent modeling of flow cytometry cell populations built upon a Bayesian hierarchical model. The model systematizes variation in location as well as shape. Expert knowledge can be incorporated through informative priors and the results can be supervised through compact and comprehensive visualizations. BayesFlow is applied to two synthetic and two real flow cytometry data sets. For the first real data set, taken from the FlowCAP I challenge, BayesFlow does not only give a gating which would place it among the top performers in FlowCAP I for this dataset, it also gives a more consistent treatment of different samples than either manual gating or other automated gating methods. The second real data set contains replicated flow cytometry measurements of samples from healthy individuals. BayesFlow gives here cell populations with clear expression patterns and small technical intra-donor variation as compared to biological inter-donor variation.

conclusionsModeling latent relations between samples through BayesFlow enables a systematic analysis of inter-sample variation. As opposed to other joint gating methods, effort is put at ensuring that the obtained partition of the data corresponds to actual cell populations, and the result is therefore directly biologically interpretable. BayesFlow is freely available at GitHub.

Indexed as

Bayes TheoremModels, MolecularComputer SimulationDatabases, FactualFlow CytometryHumans

Identifiers

PMID26755197
PMCPMC4709953

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.