Evidence map›Paper›PMID 30756325›Full record

ArticleJournal of the American Society for Mass Spectrometry2019

Mapping Lipid Fragmentation for Tailored Mass Spectral Libraries.

Paul D Hutchins, Jason D Russell, Joshua J Coon

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  3. Genetic mapping of lifespan and mitochondrial stress response inbioRxiv : the preprint server for biology · 2025
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  9. Review
  10. High-content phenotypic analysis ofbioRxiv : the preprint server for biology · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. HIGH RESOLUTION MASS SPECTROMETRY IN LIPIDOMICS.Mass spectrometry reviews · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Lipidomics from sample preparation to data analysis: a primer.Analytical and bioanalytical chemistry · 2020
    Review
  19. Article
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

3 authors at 2 institutions in 1 country.

Paul D HutchinsDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Jason D RussellGenome Center of Wisconsin, Madison, WI, 53706, USA.
Joshua J CoonDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA. jcoon@chem.wisc.edu.ORCID http://orcid.org/0000-0002-0004-8253
University of Wisconsin–Madison · USEnergy Center of Wisconsin · US

Funding

TR&D 2 Metabolic Labels for Ultraplexed Protein Quantification p. 453P41GM108538 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI COON, JOSHUA J · 2016 to 2025
$13.1M
Department of Energy DE-FC02-07ER64494Department of Energy DE-SC0018409Foundation for the National Institutes of Health P41 GM108538NIGMS NIH HHS P41 GM108538
6 · The paper itself

Abstract

Libraries of simulated lipid fragmentation spectra enable the identification of hundreds of unique lipids from complex lipid extracts, even when the corresponding lipid reference standards do not exist. Often, these in silico libraries are generated through expert annotation of spectra to extract and model fragmentation rules common to a given lipid class. Although useful for a given sample source or instrumental platform, the time-consuming nature of this approach renders it impractical for the growing array of dissociation techniques and instrument platforms. Here, we introduce Library Forge, a unique algorithm capable of deriving lipid fragment mass-to-charge (m/z) and intensity patterns directly from high-resolution experimental spectra with minimal user input. Library Forge exploits the modular construction of lipids to generate m/z transformed spectra in silico which reveal the underlying fragmentation pathways common to a given lipid class. By learning these fragmentation patterns directly from observed spectra, the algorithm increases lipid spectral matching confidence while reducing spectral library development time from days to minutes. We embed the algorithm within the preexisting lipid analysis architecture of LipiDex to integrate automated and robust library generation within a comprehensive LC-MS/MS lipidomics workflow. Graphical Abstract.

Indexed as

In silico fragmentation modelingLipid identificationsLipidomicsMass spectrometrySpectral libraries

Identifiers

PMID30756325
PMCPMC6447430
OpenAlexW2911472150

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.