Evidence map›Paper›PMID 24045582›Full record

ArticleJournal of biomolecular screening2013

Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment.

Vebjorn Ljosa, Peter D Caie, Rob Ter Horst, Katherine L Sokolnicki, Emma L Jenkins, Sandeep Daya, Mark E Roberts, Thouis R Jones, Shantanu Singh, Auguste Genovesio and 3 more

Abstract readComparative Study
In one paragraph

Article in Journal of biomolecular screening, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing 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

93 citing papers in PubMed.

  1. Article
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  17. uniDINO: Assay-independent feature extraction for fluorescence microscopy images.Computational and structural biotechnology journal · 2025
    Article
  18. Drug response in the era of precision medicine: A methodological review.Computational and structural biotechnology journal · 2025
    Review
  19. Article
  20. Systematic data analysis pipeline for quantitative morphological cell phenotyping.Computational and structural biotechnology journal · 2024
    Review

33 more citing papers are in PubMed but not listed here.

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.

Vebjorn Ljosa1Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Peter D Caie
Rob Ter Horst
Katherine L Sokolnicki
Emma L Jenkins
Sandeep Daya
Mark E Roberts
Thouis R Jones
Shantanu Singh
Auguste Genovesio
Paul A Clemons
Neil O Carragher
Anne E Carpenter

Funding

User Driven ProjectU54HG005032 · NHGRI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SCHREIBER, STUART L · 2008 to 2013
$88.1M
NHGRI NIH HHS U54 HG005032NHGRI NIH HHS U54-HG005032
6 · The paper itself

Abstract

Quantitative microscopy has proven a versatile and powerful phenotypic screening technique. Recently, image-based profiling has shown promise as a means for broadly characterizing molecules' effects on cells in several drug-discovery applications, including target-agnostic screening and predicting a compound's mechanism of action (MOA). Several profiling methods have been proposed, but little is known about their comparative performance, impeding the wider adoption and further development of image-based profiling. We compared these methods by applying them to a widely applicable assay of cultured cells and measuring the ability of each method to predict the MOA of a compendium of drugs. A very simple method that is based on population means performed as well as methods designed to take advantage of the measurements of individual cells. This is surprising because many treatments induced a heterogeneous phenotypic response across the cell population in each sample. Another simple method, which performs factor analysis on the cellular measurements before averaging them, provided substantial improvement and was able to predict MOA correctly for 94% of the treatments in our ground-truth set. To facilitate the ready application and future development of image-based phenotypic profiling methods, we provide our complete ground-truth and test data sets, as well as open-source implementations of the various methods in a common software framework.

Indexed as

Cell ShapeDrug Evaluation, PreclinicalFactor Analysis, StatisticalHumansMCF-7 CellsMicroscopy, FluorescencePhenotypeSmall Molecule LibrariesSupport Vector MachineSmall Molecule Librariesdrug profilinghigh-content screeningimage-based screeningphenotypic screening

Identifiers

PMID24045582
PMCPMC3884769

What OpenQuestion holds

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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.