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As the lipidomics field continues to advance, self-evaluation within the community is critical. Here, we performed an interlaboratory comparison exercise for lipidomics using Standard Reference Material (SRM) 1950-Metabolites in Frozen Human Plasma, a commercially available reference material. The interlaboratory study comprised 31 diverse laboratories, with each laboratory using a different lipidomics workflow. A total of 1,527 unique lipids were measured across all laboratories and consensus location estimates and associated uncertainties were determined for 339 of these lipids measured at the sum composition level by five or more participating laboratories. These evaluated lipids detected in SRM 1950 serve as community-wide benchmarks for intra- and interlaboratory quality control and method validation. These analyses were performed using nonstandardized laboratory-independent workflows. The consensus locations were also compared with a previous examination of SRM 1950 by the LIPID MAPS consortium. While the central theme of the interlaboratory study was to provide values to help harmonize lipids, lipid mediators, and precursor measurements across the community, it was also initiated to stimulate a discussion regarding areas in need of improvement.
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http://dx.doi.org/10.1194/jlr.M079012 | DOI Listing |
Talanta
August 2025
Center for Advanced Measurement Science, National Institute of Metrology, 18 Beisanhuan East Road, Beijing, 100013, PR China. Electronic address:
Digital PCR (dPCR) technology is widely utilized for various applications, including the quantification of gene mutations and copy number variations. Certified reference materials (CRMs) play a critical role in improving the comparability of dPCR results, establishing SI-traceable copy number concentration values for dPCR calibration remains a key challenge due to the limited availability of CRMs value-assigned by higher-order, independent methods. To tackle this issue, a linearized plasmid DNA reference material (RM) was developed and rigorously characterized through an interlaboratory comparison involving three national measurement institutes (NMIs) from China (NIM), South Korea (KRISS), and Japan (NMIJ).
View Article and Find Full Text PDFSci Total Environ
August 2025
Health Sciences North Research Institute, Sudbury, Ontario, Canada.
Reliable and comparable data from multiple laboratories are essential for networks relying on reverse transcription quantitative polymerase chain reaction (RT-qPCR)-based surveillance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genetic material in wastewater. Large-scale networks, such as those spanning Canada and the United States, depend on multiple laboratories deploying varied methods. However, the comparability of these methods and implications for data interoperability have not been rigorously examined.
View Article and Find Full Text PDFSci Rep
August 2025
School of Biosciences, Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, United Kingdom.
The activity of α-amylases is frequently determined using a single-point assay at 20 °C. Previous work within INFOGEST "Working Group 5 - Starch digestion and amylases" identified significant interlaboratory variation with this protocol. The current study aimed to evaluate the repeatability (intralaboratory precision) and reproducibility (interlaboratory precision), measured as coefficients of variation (CVs), of a newly optimized protocol version based on four time-point measurements at 37 °C.
View Article and Find Full Text PDFDoc Ophthalmol
August 2025
Department of Electrophysiology, Moorfields Eye Hospital, London, UK.
Visual evoked potentials (VEPs) are electrophysiologic responses to pattern or flash stimuli, recorded over the occiput. VEPs can provide information regarding the function of the visual system and are valuable in the diagnosis and investigation of optic nerve disease or post-retinal visual pathway dysfunction. The ISCEV VEP Standard specifies stimulus and recording conditions for three basic types of recording: (1) Pattern-reversal VEPs elicited by checkerboard stimuli with large 1° (degree) and small 0.
View Article and Find Full Text PDFAppl Radiat Isot
November 2025
Department of Nuclear Engineering, School of Nuclear and Allied Sciences, College of Basic and Applied Sciences, University of Ghana, P.O. Box AE1, Atomic Energy, Kwabenya-Accra, Ghana.
We present an improved neutron activation analysis (NAA) protocol tailored for low-power (34 kW) Ghana Research Reactor-1 (GHARR-1), a miniature neutron source reactor (MNSR). This protocol is designed for routine multi-elemental analysis of sediment/soil samples. It requires 150 mg of analyte per irradiation section, and strategically adjusts irradiation and counting schemes based on radionuclide half-lives.
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