Evidence map›Paper›PMID 28327978›Full record

ArticleGigaScience2017

A dataset of images and morphological profiles of 30 000 small-molecule treatments using the Cell Painting assay.

Mark-Anthony Bray, Sigrun M Gustafsdottir, Mohammad H Rohban, Shantanu Singh, Vebjorn Ljosa, Katherine L Sokolnicki, Joshua A Bittker, Nicole E Bodycombe, Vlado Dancík, Thomas P Hasaka and 10 more

Abstract readDataset
In one paragraph

Article in GigaScience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing 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

96 citing papers in PubMed.

  1. Article
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  17. Article
  18. MGMG: Cell Morphology-Guided Molecule Generation for Drug Discovery.bioRxiv : the preprint server for biology · 2025
    Article
  19. Article
  20. Article

36 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

20 authors.

Mark-Anthony BrayImaging Platform.
Sigrun M GustafsdottirChemical Biology and Therapeutics Science Program.
Mohammad H RohbanImaging Platform.
Shantanu SinghImaging Platform.
Vebjorn LjosaImaging Platform.
Katherine L SokolnickiImaging Platform.
Joshua A BittkerCenter for the Development of Therapeutics.
Nicole E BodycombeChemical Biology and Therapeutics Science Program.
Vlado DancíkChemical Biology and Therapeutics Science Program.
Thomas P HasakaCenter for the Development of Therapeutics.
Cindy S HonChemical Biology and Therapeutics Science Program.
Melissa M KempChemical Biology and Therapeutics Science Program.
Kejie LiChemical Biology and Therapeutics Science Program.
Deepika WalpitaChemical Biology and Therapeutics Science Program.
Mathias J WawerChemical Biology and Therapeutics Science Program.
Todd R GolubCancer Program, Broad Institute of Harvard and MIT, Cambridge, MA, USA, 02142.
Stuart L SchreiberChemical Biology and Therapeutics Science Program.
Paul A ClemonsChemical Biology and Therapeutics Science Program.
Alykhan F ShamjiChemical Biology and Therapeutics Science Program.
Anne E CarpenterImaging Platform.

Funding

Extracting rich information from biological imagesR35GM122547 · NIGMS · BROAD INSTITUTE, INC. · PI Anne E. Carpenter · 2017 to 2026
$6.2M
NIGMS NIH HHS R35 GM122547
6 · The paper itself

Abstract

Background: Large-scale image sets acquired by automated microscopy of perturbed samples enable a detailed comparison of cell states induced by each perturbation, such as a small molecule from a diverse library. Highly multiplexed measurements of cellular morphology can be extracted from each image and subsequently mined for a number of applications. Findings: This microscopy dataset includes 919 265 five-channel fields of view, representing 30 616 tested compounds, available at "The Cell Image Library" (CIL) repository. It also includes data files containing morphological features derived from each cell in each image, both at the single-cell level and population-averaged (i.e., per-well) level; the image analysis workflows that generated the morphological features are also provided. Quality-control metrics are provided as metadata, indicating fields of view that are out-of-focus or containing highly fluorescent material or debris. Lastly, chemical annotations are supplied for the compound treatments applied. Conclusions: Because computational algorithms and methods for handling single-cell morphological measurements are not yet routine, the dataset serves as a useful resource for the wider scientific community applying morphological (image-based) profiling. The dataset can be mined for many purposes, including small-molecule library enrichment and chemical mechanism-of-action studies, such as target identification. Integration with genetically perturbed datasets could enable identification of small-molecule mimetics of particular disease- or gene-related phenotypes that could be useful as probes or potential starting points for development of future therapeutics.

Indexed as

Image Processing, Computer-AssistedSmall Molecule LibrariesCell LineCellsHumansSmall Molecule Librariescellular morphologyhigh-content screeningimage-based screeningphenotypic profilingsmall-molecule libraryU2OS

Identifiers

PMID28327978
PMCPMC5721342

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.