Evidence map›Paper›PMID 24686220›Full record

ArticleJournal of visualized experiments : JoVE2014

Rapid analysis and exploration of fluorescence microscopy images.

Benjamin Pavie, Satwik Rajaram, Austin Ouyang, Jason M Altschuler, Robert J Steininger, Lani F Wu, Steven J Altschuler

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

7 authors at 4 institutions in 1 country.

Benjamin PavieGreen Center for Systems Biology, UT Southwestern Medical Center.
Satwik RajaramGreen Center for Systems Biology, UT Southwestern Medical Center.
Austin OuyangAdvanced Imaging Research Center, UT Southwestern Medical Center.
Jason M AltschulerGreen Center for Systems Biology, UT Southwestern Medical Center; Princeton University.
Robert J SteiningerGreen Center for Systems Biology, UT Southwestern Medical Center.
Lani F WuGreen Center for Systems Biology, UT Southwestern Medical Center; Lani.Wu@utsouthwestern.edu.
Steven J AltschulerGreen Center for Systems Biology, UT Southwestern Medical Center; Steven.Altschuler@utsouthwestern.edu.
Center for Systems Biology · USSouthwestern Medical CenterSouthwestern Medical Center · USAdvanced Imaging Research (United States) · US

Funding

The design principles underlying cell polarity in yeastR01GM071794 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI ALTSCHULER, STEVEN J · 2004 to 2012
$2.3M
Lung cancer heterogeneity and its impact on drug resistance.R01CA133253 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI ALTSCHULER, STEVEN J · 2010 to 2015
$2.3M
Image based phenotypic profiling of single-cell responses to perturbationsR01GM081549 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI WU, LANI F · 2007 to 2011
$1.7M
Turnkey solution for image phenotype classificationR01GM085442 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI ALTSCHULER, STEVEN J · 2008 to 2011
$1.2M
NCI NIH HHS CA133253NCI NIH HHS R01 CA133253NIGMS NIH HHS R01 GM071794NIGMS NIH HHS R01 GM081549NIGMS NIH HHS R01 GM085442
6 · The paper itself

Abstract

Despite rapid advances in high-throughput microscopy, quantitative image-based assays still pose significant challenges. While a variety of specialized image analysis tools are available, most traditional image-analysis-based workflows have steep learning curves (for fine tuning of analysis parameters) and result in long turnaround times between imaging and analysis. In particular, cell segmentation, the process of identifying individual cells in an image, is a major bottleneck in this regard. Here we present an alternate, cell-segmentation-free workflow based on PhenoRipper, an open-source software platform designed for the rapid analysis and exploration of microscopy images. The pipeline presented here is optimized for immunofluorescence microscopy images of cell cultures and requires minimal user intervention. Within half an hour, PhenoRipper can analyze data from a typical 96-well experiment and generate image profiles. Users can then visually explore their data, perform quality control on their experiment, ensure response to perturbations and check reproducibility of replicates. This facilitates a rapid feedback cycle between analysis and experiment, which is crucial during assay optimization. This protocol is useful not just as a first pass analysis for quality control, but also may be used as an end-to-end solution, especially for screening. The workflow described here scales to large data sets such as those generated by high-throughput screens, and has been shown to group experimental conditions by phenotype accurately over a wide range of biological systems. The PhenoBrowser interface provides an intuitive framework to explore the phenotypic space and relate image properties to biological annotations. Taken together, the protocol described here will lower the barriers to adopting quantitative analysis of image based screens.

Indexed as

ActinsCell Culture TechniquesDNAFluorescent DyesHeLa CellsHumansImage Processing, Computer-AssistedMicroscopy, FluorescenceSoftwareStaining and LabelingTubulinActinsDNAFluorescent DyesTubulin

Identifiers

PMID24686220
PMCPMC4390293
OpenAlexW1980223929

What OpenQuestion holds

Textmetadata
LicenceTDM
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.