ArticleACS omega2026
Advancing Colorimetric Analysis in Enzyme-Linked Immunosorbent Assays: Harnessing Nonlinear Regression for Improved Accuracy and Predictive Performance.
Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Artificial Intelligence as a Discovery Engine for Routine Molecular Techniques: Extracting Biological Insight from Western Blotting, ELISA, Immunostaining, and Immunoprecipitation.Cell biochemistry and biophysics · 2026Review
Corrections and comments
- Erratum issued
Authors and funding
7 authors.
Funding
Abstract
Smartphone-based colorimetric enzyme-linked immunosorbent assay (ELISA) readers have emerged as a cost-effective and portable alternative to conventional spectrophotometric systems, especially for use in resource-limited and point-of-care settings. In our previous work, we developed a digital image colorimetry platform integrated with a 3D-printed optomechanical system and smartphone imaging, achieving high diagnostic accuracy for cancer cell lines through linear regression modeling of red, green, and blue (RGB) intensities. While effective, this linear approach could not fully capture the nonlinear relationships intrinsic to enzymatic colorimetric reactions and light-matter interactions. In this study, we present a significant enhancement to our prior model by implementing a nonlinear machine learning framework, eXtreme gradient boosting (XGBoost), to better predict optical densities from smartphone-captured RGB data. Utilizing the same hardware platform and experimental protocol as our earlier system, we extracted RGB values from ELISA images under RGB backlighting and then expanded the feature space through engineered transformations. These features were used to train and validate the XGBoost model on multiple human cancer cell lines (HE4, PC3, 5637, and ACHN). Our XGBoost model achieved exceptional predictive performance with
Identifiers
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Registered trials
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.