ArticleAnalytical and bioanalytical chemistry2025
Examining the effects of analytical replication on data quality in a non-targeted analysis experiment.
Article in Analytical and bioanalytical chemistry, 2025. 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
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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
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Who cites it
1 citing paper in PubMed.
- [Assessment on data processing methods for nontarget identification of per- and polyfluoroalkyl substances using liquid chromatography-high-resolution mass spectrometry].Se pu = Chinese journal of chromatography · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
12 authors.
Funding
Abstract
Non-targeted analysis (NTA) methods are integral to environmental monitoring given their ability to expand measurable chemical space beyond that of traditional targeted methods. Such vast quantities of NTA data are generated that exhaustive manual review is generally unfeasible. Computational tools facilitate automated data processing, but cannot always distinguish real signals (i.e., originating from a chemical in a sample) from artifacts. Replicate analysis is recommended to aid data review, but as NTA studies become larger, the cost of analytical replication becomes untenable. A need therefore exists for examination of information penalties associated with reduced replication. To investigate this issue, using an existing NTA dataset, we performed over 70,000 simulations of variable replication designs and calculated false discovery rates (FDRs) and false negative rates (FNRs) for NTA features and occurrences. We used regression models to explore associations between replication percentage and FDR/FNR, and to test whether rates were affected by NTA feature attributes. Inverse relationships were generally observed between replication percentage and FDR/FNR, such that lower replication yielded higher information penalties. Significant increases in FDR/FNR were observed for suspected per- and polyfluoroalkyl substances (PFAS) compared to non-PFAS, highlighting the potential for differences in information penalties across feature groups. Specific quantitative information penalties are expected to be unique for each NTA study based on sample type and workflow. The methods presented here can support future pilot-scale investigations that will inform the required level of replication in full-scale studies.
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