Evidence map›Paper›PMID 33135052›Full record

ArticleBioinformatics (Oxford, England)2021

Agile workflow for interactive analysis of mass cytometry data.

Julia Casado, Oskari Lehtonen, Ville Rantanen, Katja Kaipio, Luca Pasquini, Antti Häkkinen, Elenora Petrucci, Johanna Hynninen, Sakari Hietanen, Olli Carpén and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Computational Methods for Single-Cell Proteomics.Annual review of biomedical data science · 2023
    Review
  5. ANPELA: Significantly Enhanced Quantification Tool for Cytometry-Based Single-Cell Proteomics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  6. Article
  7. Review
  8. Article
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

13 authors at 5 institutions in 3 countries.

Julia CasadoResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Oskari LehtonenResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Ville RantanenResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Katja KaipioDepartment of Pathology, University of Turku, Turku, Finland.
Luca PasquiniIstituto Superiore di Sanità, Core Facilities, Rome, Italy.
Antti HäkkinenResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Elenora PetrucciIstituto Superiore di Sanità, Department of Haematology, Rome, Italy.
Johanna HynninenDepartment of Obstetrics and Gynecology, Turku University Hospital, University of Turku, Turku, Finland.
Sakari HietanenDepartment of Obstetrics and Gynecology, Turku University Hospital, University of Turku, Turku, Finland.
Olli CarpénDepartment of Pathology, University of Turku, Turku, Finland.
Mauro BiffoniIstituto Superiore di Sanità, Department of Haematology, Rome, Italy.
Anniina FärkkiläResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Sampsa HautaniemiResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
University of Helsinki · FIIstituto Superiore di Sanità · ITUniversity of Turku · FIHarvard University · USTurku University Hospital · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationSingle-cell proteomics technologies, such as mass cytometry, have enabled characterization of cell-to-cell variation and cell populations at a single-cell resolution. These large amounts of data, require dedicated, interactive tools for translating the data into knowledge.

resultsWe present a comprehensive, interactive method called Cyto to streamline analysis of large-scale cytometry data. Cyto is a workflow-based open-source solution that automates the use of state-of-the-art single-cell analysis methods with interactive visualization. We show the utility of Cyto by applying it to mass cytometry data from peripheral blood and high-grade serous ovarian cancer (HGSOC) samples. Our results show that Cyto is able to reliably capture the immune cell sub-populations from peripheral blood and cellular compositions of unique immune- and cancer cell subpopulations in HGSOC tumor and ascites samples. AVAILABILITYAND IMPLEMENTATION: The method is available as a Docker container at https://hub.docker.com/r/anduril/cyto and the user guide and source code are available at https://bitbucket.org/anduril-dev/cyto. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

ProteomicsSoftwareData Interpretation, StatisticalWorkflow

Identifiers

PMID33135052
PMCPMC8189671
OpenAlexW3097372521

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.