Evidence map›Paper›PMID 35585588›Full record

ArticleVirology journal2022

Non-linear transformation of enzyme-linked immunosorbent assay (ELISA) measurements allows usage of linear models for data analysis.

Thomas M Lange, Maria Rotärmel, Dominik Müller, Gregory S Mahone, Friedrich Kopisch-Obuch, Harald Keunecke, Armin O Schmitt

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Article in Virology journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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.

Thomas M LangeBreeding Informatics Group, University of Göttingen, Margarethe von Wrangell-Weg 7, 37075, Göttingen, Germany.
Maria RotärmelBreeding Informatics Group, University of Göttingen, Margarethe von Wrangell-Weg 7, 37075, Göttingen, Germany.
Dominik MüllerKWS SAAT SE & Co. KGaA, 37574, Einbeck, Germany.
Gregory S MahoneKWS SAAT SE & Co. KGaA, 37574, Einbeck, Germany.
Friedrich Kopisch-ObuchKWS SAAT SE & Co. KGaA, 37574, Einbeck, Germany.
Harald KeuneckeKWS SAAT SE & Co. KGaA, 37574, Einbeck, Germany.
Armin O SchmittBreeding Informatics Group, University of Göttingen, Margarethe von Wrangell-Weg 7, 37075, Göttingen, Germany. armin.schmitt@uni-goettingen.de.ORCID 0000-0002-4910-9467

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn research questions such as in resistance breeding against the Beet necrotic yellow vein virus it is of interest to compare the virus concentrations of samples from different groups. The enzyme-linked immunosorbent assay (ELISA) counts as the standard tool to measure virus concentrations. Simple methods for data analysis such as analysis of variance (ANOVA), however, are impaired due to non-normality of the resulting optical density (OD) values as well as unequal variances in different groups.

methodsTo understand the relationship between the OD values from an ELISA test and the virus concentration per sample, we used a large serial dilution and modelled its non-linear form using a five parameter logistic regression model. Furthermore, we examined if the quality of the model can be increased if one or several of the model parameters are defined beforehand. Subsequently, we used the inverse of the best model to estimate the virus concentration for every measured OD value.

resultsWe show that the transformed data are essentially normally distributed but provide unequal variances per group. Thus, we propose a generalised least squares model which allows for unequal variances of the groups to analyse the transformed data.

conclusionsANOVA requires normally distributed data as well as equal variances. Both requirements are not met with raw OD values from an ELISA test. A transformation with an inverse logistic function, however, gives the possibility to use linear models for data analysis of virus concentrations. We conclude that this method can be applied in every trial where virus concentrations of samples from different groups are to be compared via OD values from an ELISA test. To encourage researchers to use this method in their studies, we provide an R script for data transformation as well as the data from our trial.

Indexed as

Data AnalysisEnzyme-Linked Immunosorbent AssayLinear ModelsLogistic ModelsBeet necrotic yellow vein virusBNYVVData analysisGeneralised least squares modelLogistic regressionSerial dilutionVirus concentration

Identifiers

PMID35585588
PMCPMC9118653

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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.