Evidence map›Paper›PMID 39557686›Full record

ArticleAnalytical and bioanalytical chemistry2025

Effect of different pooled qc samples on data quality during an inter-batch experiment in untargeted UHPLC-HRMS analysis on two different MS platforms.

Mélina Ramos, Valérie Camel, Even Le Roux, Soha Farah, Mathieu Cladiere

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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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 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

5 authors.

Mélina RamosUniversité Paris-Saclay, INRAE, AgroParisTech, UMR SayFood, 91120, Palaiseau, France.
Valérie CamelUniversité Paris-Saclay, INRAE, AgroParisTech, UMR SayFood, 91120, Palaiseau, France.
Even Le RouxUniversité Paris-Saclay, INRAE, AgroParisTech, UMR SayFood, 91120, Palaiseau, France.
Soha FarahUniversité Paris-Saclay, INRAE, AgroParisTech, UMR SayFood, 91120, Palaiseau, France.
Mathieu CladiereUniversité Paris-Saclay, INRAE, AgroParisTech, UMR SayFood, 91120, Palaiseau, France. mathieu.cladiere@agroparistech.fr.ORCID http://orcid.org/0000-0002-7555-0918

Funding

Agence Nationale de la Recherche ANR-21-CE21-0002
6 · The paper itself

Abstract

Quality control (QC) samples are commonly used in metabolomics approaches for three main reasons: (i) the initial conditioning of the column; (ii) the correction of analytical drift especially between batches; and (iii) the evaluation of measurement precision. In practice, there are several ways to prepare and conserve QC samples. The most common in untargeted metabolomics is to pool samples after or before extraction, in order to obtain pooled QC samples accounting, respectively, for analytical variance or for both analytical and sample preparation variances. In this study, focusing on untargeted analysis of tea (Camellia sinensis) leaves, we compared three ways of preparing pooled QC samples (two usual and one unusual QC sample preparations) and their efficiency to improve data quality in terms of inter-batch correction, measurement precision, and VIP candidates selection on datasets obtained using two mass spectrometry (MS) technologies (Orbitrap and time of flight (QToF)). We also investigated the effect of data processing modalities, based on the different QC preparations, on data loss and on the global structure of the datasets. Generally, our results show that usual QC sample preparation leads to comparable datasets quality in terms of precision and dispersion on both MS instruments. They also show that QC preparation is crucial for VIP selection; in fact, up to 54% of biomarkers candidates were specific of the QC preparation type used for data processing.

Indexed as

Mass SpectrometryMetabolomicsQuality ControlCamellia sinensisChromatography, High Pressure LiquidData AccuracyPlant LeavesInter-batch correctionLiquid chromatography (LC)Mass spectrometry (MS)Non-targeted analysesQuality control (QC)Tea leaves (dry)

Identifiers

PMID39557686

What OpenQuestion holds

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Registered trials

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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.