Evidence map›Paper›PMID 32384576›Full record

ArticleRapid communications in mass spectrometry : RCM2020

MGMS2: Membrane glycolipid mass spectrum simulator for polymicrobial samples.

So Young Ryu, George A Wendt, Robert K Ernst, David R Goodlett

Abstract read
In one paragraph

Article in Rapid communications in mass spectrometry : RCM, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. 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

4 authors.

So Young RyuSchool of Community Health Sciences, University of Nevada, Reno, NV, USA.ORCID https://orcid.org/0000-0003-2347-7015
George A WendtSchool of Community Health Sciences, University of Nevada, Reno, NV, USA.
Robert K ErnstDepartment of Microbial Pathogenesis, University of Maryland, Baltimore, MD, USA.
David R GoodlettDepartment of Microbial Pathogenesis, University of Maryland, Baltimore, MD, USA.

Funding

Outreach/Diversity/Pipeline ProjectP20GM103440 · NIGMS · UNIVERSITY OF NEVADA RENO · PI Eduardo A Robleto · 2012 to 2026
$58.0M
MS Diagnostic Bacterial Identification LibraryR01AI147314 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI ERNST, ROBERT K, GOODLETT, DAVID ROBINSON · 2020 to 2024
$2.3M
MS diagnostic bacterial identification libraryR01GM111066 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERNST, ROBERT K, GOODLETT, DAVID ROBINSON · 2014 to 2017
$1.2M
HKLE-seq: an enrichment method for unbiased amplification and next-generation sequencing of all HERV-K and SVA (HKLE) insertion breakpoints genome-wide in human DNA samplesR15GM126562 · NIGMS · UNIVERSITY OF NEVADA RENO · PI RYU, SO YOUNG · 2018 to 2018
$430k
European Regional Development Fund (MAB/2017/03), University of Gdansk International Research Agendas programNIAID NIH HHS R01 AI147314NIGMS NIH HHS 1R01GM111066-01NIGMS NIH HHS 1R15GM126562-01NIGMS NIH HHS GM103440NIGMS NIH HHS P20 GM103440NIGMS NIH HHS R01 GM111066NIGMS NIH HHS R15 GM126562University of Nevada Reno, School of Medicine Faculty Development Award
6 · The paper itself

Abstract

rationalePolymicrobial samples present unique challenges for mass spectrometric identification. A recently developed glycolipid technology has the potential to accurately identify individual bacterial species from polymicrobial samples. In order to develop and validate bacterial identification algorithms (e.g. machine learning) using this glycolipid technology, generating a large number of various polymicrobial samples can be beneficial, but it is costly and labor-intensive. Here, we propose an alternative cost-effective approach that generates realistic in silico polymicrobial glycolipid mass spectra.

methodsWe introduce MGMS2 (membrane glycolipid mass spectrum simulator) as a simulation software package that generates in silico polymicrobial membrane glycolipid matrix-assisted laser desorption/ionization time-of-flight mass spectra. Unlike currently available simulation algorithms for polymicrobial mass spectra, the proposed algorithm considers errors in m/z values and variances of intensity values, occasions of missing signature ions, and noise peaks. To our knowledge, this is the first stand-alone bacterial membrane glycolipid mass spectral simulator. MGMS2 software and its manual are freely available as an R package. An interactive MGSM2 app that helps users explore various simulation parameter options is also available.

resultsWe demonstrated the performance of MGSM2 using six microbes. The software generated in silico glycolipid mass spectra that are similar to real polymicrobial glycolipid mass spectra. The maximum correlation between in silico mass spectra generated by MGMS2 and the real polymicrobial mass spectrum was about 87%.

conclusionsWe anticipate that MGMS2, which considers spectrum-to-spectrum variation, will advance the bacterial algorithm development for polymicrobial samples.

Indexed as

SoftwareBacteriaBacteriological TechniquesComputational BiologyComputer SimulationGlycolipidsMembrane LipidsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationWorkflowGlycolipidsMembrane Lipids

Identifiers

PMID32384576
PMCPMC7466374

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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.