bioRxivBioinformaticsPreprint
The Everything Bagel Feature Finder: Ultra-fast automated feature finding for untargeted metabolomics
Yourae ShiniD, Yasin El AbieadiD, Alan K. JarmuschiD, Michael J. StrobeliD, Paul E. AbrahamiD, S.G. ThurmoniD, Deepa D. AcharyaiD, Allegra T. AroniD, Aivett Bilbao PenaiD, Benjamin P. BoweniD, Corey D. BroecklingiD, Christopher J. BrowniD, Vincent Charron‐LamoureuxiD, Xingyuan CheniD, Tito DamianiiD, Alex DotyiD, Xiuxia DuiD, Neha GargiD, Stilianos Papadopoulos LambidisiD, Laura‐Isobel McCalliD, Kaylie I. Kirkwood‐DonelsoniD, Trent R. NortheniD, Jessica E. PrenniiD, Emma E. RennieiD, Oliver B. ViningiD, , Mingxun WangiD
Abstract
Metabolomics studies are increasingly being applied with hundreds to thousands, even tens of thousands of samples that demand rapid, automated data processing while maintaining analytical sensitivity or quantitative accuracy. A major computational bottleneck is feature finding, which is the transformation of LC-MS and LC-MS/MS data into a set of analyte signals aligned and quantified across samples. Feature finding can be computationally intensive and often requires manual iterative parameter optimization. To accelerate this process, we present the Everything Bagel (EB) feature finder, an ultra-fast automated feature finding tool that integrates feature detection, retention-time alignment, and gap filling designed for run-time and memory efficiency. We benchmarked EB against two automated feature finding methods on eight benchmarking datasets. Specifically, we evaluated these three feature finding methods by measuring spike-in standard detection coverage, dilution series quantification accuracy, and yeast 12C/13C credentialed features. In this evaluation, the EB feature finder achieved performance comparable to, and often exceeding, existing methods while requiring up to 150-fold lower CPU hours and up to 113-fold lower wall time. We further demonstrated the bioanalytical validity of EB by reanalyzing published datasets used for biomarker discovery and reproduced biologically significant features that matched the published findings using manually tuned feature finding settings. Taken along with the speed improvements, we anticipate EB will enhance the ability to automatically analyze datasets with thousands to tens of thousands of samples for the community.
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- TIMS-Bench: Towards community standards for benchmarking untargeted trapped ion mobility metabolomics tools and datasets
Prajit Rajkumar, Yojana Gadiya, … Biswapriya B. Misra·bioRxiv·May 27, 2026
- Deep Learning assisted Peak Curation for large scale LC-MS Metabolomics
Yoann Gloaguen, Jennifer Kirwan, Dieter Beule·Analytical ChemistryPeer-reviewed·Mar 15, 2022
- BLINK: Ultrafast tandem mass spectrometry cosine similarity scoring
Thomas V. Harwood, Daniel G. C. Treen, … Benjamin P. Bowen·bioRxiv·Feb 14, 2023
- A novel paradigm for optimal mass feature peak picking in large scale LC-MS datasets using the isopair: isoLock, autoCredential and anovAlign
Allen Hubbard, Louis Connelly, … Ivan R. Baxter·bioRxiv·Dec 5, 2021
- MetaboCensoR: A Shiny Application for Data Filtering in Untargeted LC-MS Metabolomics to Enhance Interpretability
I. V. Plyushchenko, Tal Luzzatto‐Knaan·bioRxiv·Sep 22, 2026
- Homologue Series Detection and Management in LC-MS data with homologueDiscoverer
Kevin Mildau, Justin J. J. van der Hooft, … Christoph Büschl·BioinformaticsPeer-reviewed·Sep 23, 2022