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Pujos-Guillot, E.

Publications and source records attributed to Pujos-Guillot, E..

2 recordsLinked to original sources

A benchmarking workflow for assessing the reliability of batch correction methods

One of the most pervasive challenges in large-scale untargeted metabolomics is short and long-term analytical variability introducing the necessity of batch effect correction. In this context, several strategies and methods have been developed to limit those effects, either by monitoring the data generation process to maximize reproducibility or by applying post-analysis data correction. Different evaluation frameworks, either assessing the degree of bias in the data through visual tools or quantitative indicators, or evaluating the prediction performance of known biomarkers, were also proposed. However, there is currently no clear consensus on how to evaluate batch correction methods. This work offers a strategy to assess multiple dimensions of batch correction efficiency within a comprehensive and reliable framework, designed to assess the effectiveness and reliability of batch correction methods. Based on Mahalanobis Conformity Index (MCI), it provides a multivariate and covariance-aware metric to quantify within- and between-batch variability. Additionally, it combines visualization techniques (Principal Component Analysis (PCA) and Multivariate INTegrative (MINT) PCA) with numerical indicators (batch dispersion, Coefficient of Variation), supporting both multidimensional and metabolite-specific evaluations. Lastly, this novel approach integrates statistical tools alongside chemistry-based metrics for method overfitting and overcorrection assessment. Applied within a use case for comparing LOESS-based and ComBat correction methods, the present workflow provided a structured approach to systematically assess the reliability of batch corrections, ensuring both data intercomparability and biological relevance in metabolomics studies. Author summaryThe assessment of batch correction is a challenge in metabolomics, where there is no consensus for a define strategy, making it a complex task. However, knowing the impact of batch correction on the datasets and consecutive possible impact on downstream statistical analyses, providing a reliable framework for its assessment is a cornerstone for reproducible results. The objective of the present work was to provide a framework and a set of interpretation tools combining numerical indicators, as well as diagnostic plots, for assessing the reliability of batch correction methods. We introduced a robust evaluation framework centered on the Mahalanobis Conformity Index, providing a multivariate and covariance-aware metric to quantify within- and between-batch variability. By coupling this index with visual tools (based on Principal Component Analysis (PCA) and Multivariate INTegrative (MINT) PCA), as well as compound-level diagnostics, we enabled a fine-grained and interpretable comparison of correction strategies, highlighting their strengths and potential pitfalls.

bioinformatics↗

WiPP: Workflow for improved Peak Picking for Gas Chromatography-Mass Spectrometry (GC-MS) data

Lack of reliable peak detection impedes automated analysis of large scale GC-MS metabolomics datasets. Performance and outcome of individual peak-picking algorithms can differ widely depending on both algorithmic approach and parameters as well as data acquisition method. Comparing and contrasting between algorithms is thus difficult. Here we present a workflow for improved peak picking (WiPP), a parameter optimising, multi-algorithm peak detection for GC-MS metabolomics. WiPP evaluates the quality of detected peaks using a machine learning-based classification scheme based on seven peak classes. The quality information returned by the classifier for each individual peak is merged with results from different peak detection algorithms to create one final high quality peak set for immediate down stream analysis. Medium and low quality peaks are kept for further inspection. By applying WiPP to standard compound mixes and a complex biological dataset we demonstrate that peak detection is improved through the novel way to assign peak quality, an automated parameter optimisation, and results integration across different embedded peak picking algorithms. Furthermore, our approach can provide an impartial performance comparison of different peak picking algorithms. WiPP is freely available on GitHub (https://github.com/bihealth/WiPP) under MIT licence.

bioinformatics↗