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Misconduct Detection — Evolving Methods & Lessons from 15 Years of Scientific Image Sleuthing

Published online by Cambridge University Press:  27 March 2025

Paul S. Brookes*
Affiliation:
Department of Anesthesiology, University of Rochester Medical Center, Rochester, New York, United States
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Abstract

I have been investigating and reporting on image manipulation in the bioscience literature since 2011. During this time, several new tools have emerged to streamline the processes of image analysis and reporting. When presenting and discussing examples of scientific image manipulation, a common question is “how do you find this stuff?” Herein, I outline common software and other utilities — a toolbox for discovery and reporting of problematic scientific images and other data. This may serve as a useful reference for those seeking to enhance the effective removal of problematic papers from the bioscience literature.

Information

Type
Symposium Articles
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - ND
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-nc-nd/4.0), which permits non-commercial re-use, distribution, and reproduction in any medium, provided that no alterations are made and the original article is properly cited. The written permission of Cambridge University Press must be obtained prior to any commercial use and/or adaptation of the article.
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of American Society of Law, Medicine & Ethics
Figure 0

Figure 1. Example of the curves feature in Adobe Photoshop to adjust brightness of different components of an image (shadows, midtones, highlights).

Figure 1

Figure 2. Application of a color gradient map in Adobe Photoshop. Original western blot image on the left, recolored version in the center. Menu for selecting gradient options on the right.

Figure 2

Figure 3. Histogram function in Adobe Photoshop. Different bands in the western blot image (highlighted in red boxes) are selected and the histogram function is applied to the region of interest. Resulting histograms show the abundance of pixels at each shade (black on the left, white on the right). The 2nd and 3rd bands from the left have histograms that show a sharp cut-off before black is reached on the x-axis.

Figure 3

Figure 4. Densitometry analysis in ImageJ software. First, vertical lanes within the western blot image (left) are selected, as shown by yellow boxes. The red arrow here indicates a band of interest. Second, a densitometry plot is graphed for each lane (shown on the right), with the height of each peak corresponding to the darkness of the band (see scale lower right). The red arrow indicates the band of interest. Lastly, the area of the peaks is calculated (table at lower left).

Figure 4

Figure 5. Saturation of western blot bands in densitometry analysis. Ideally, densitometry peaks should be Gaussian without “clipped” tops. In the example shown here, the band on the left has a rounded peak on its density graph, indicating saturation of the signal.

Figure 5

Table 1. Taxonomy used by the author, covering typical examples of image manipulation in bioscience papers