Evidence map›Paper›PMID 35758781›Full record

ArticleBioinformatics (Oxford, England)2022

psupertime: supervised pseudotime analysis for time-series single-cell RNA-seq data.

Will Macnair, Revant Gupta, Manfred Claassen

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

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  10. Reversing T cell dysfunction in a novelFrontiers in immunology · 2026
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  16. TSPAN4Frontiers in immunology · 2025
    Article
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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

3 authors.

Will MacnairInstitute of Molecular Systems Biology, Department of Biology, ETH Zurich, Zurich 8093, Switzerland.
Revant GuptaInner Medicine I, Faculty of Medicine, University of Tübingen, University Hospital Tübingen, 72074, Germany.
Manfred ClaassenInner Medicine I, Faculty of Medicine, University of Tübingen, University Hospital Tübingen, 72074, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationImprovements in single-cell RNA-seq technologies mean that studies measuring multiple experimental conditions, such as time series, have become more common. At present, few computational methods exist to infer time series-specific transcriptome changes, and such studies have therefore typically used unsupervised pseudotime methods. While these methods identify cell subpopulations and the transitions between them, they are not appropriate for identifying the genes that vary coherently along the time series. In addition, the orderings they estimate are based only on the major sources of variation in the data, which may not correspond to the processes related to the time labels.

resultsWe introduce psupertime, a supervised pseudotime approach based on a regression model, which explicitly uses time-series labels as input. It identifies genes that vary coherently along a time series, in addition to pseudotime values for individual cells, and a classifier that can be used to estimate labels for new data with unknown or differing labels. We show that psupertime outperforms benchmark classifiers in terms of identifying time-varying genes and provides better individual cell orderings than popular unsupervised pseudotime techniques. psupertime is applicable to any single-cell RNA-seq dataset with sequential labels (e.g. principally time series but also drug dosage and disease progression), derived from either experimental design and provides a fast, interpretable tool for targeted identification of genes varying along with specific biological processes. AVAILABILITY AND IMPLEMENTATION: R package available at github.com/wmacnair/psupertime and code for results reproduction at github.com/wmacnair/psupplementary. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Single-Cell AnalysisSoftwareGene Expression ProfilingRNA-SeqSequence Analysis, RNATime FactorsTranscriptome

Identifiers

PMID35758781
PMCPMC9235474

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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.