Evidence map›Paper›PMID 31407893›Full record

ArticleAnalytical chemistry2019

The Aristotle Classifier: Using the Whole Glycomic Profile To Indicate a Disease State.

David Hua, Milani Wijeweera Patabandige, Eden P Go, Heather Desaire

Abstract read
In one paragraph

Article in Analytical chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Software tools, databases and resources in metabolomics: updates from 2018 to 2019.Metabolomics : Official journal of the Metabolomic Society · 2020
    Review
  9. Article
  10. Review
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.

David HuaDepartment of Chemistry , University of Kansas , Lawrence , Kansas 66045 , United States.
Milani Wijeweera PatabandigeDepartment of Chemistry , University of Kansas , Lawrence , Kansas 66045 , United States.
Eden P GoDepartment of Chemistry , University of Kansas , Lawrence , Kansas 66045 , United States.
Heather DesaireDepartment of Chemistry , University of Kansas , Lawrence , Kansas 66045 , United States.ORCID 0000-0002-2181-0112

Funding

Mass Spectrometry Measurements for Complex PTMsR35GM130354 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI DESAIRE, HEATHER R · 2019 to 2023
$1.9M
Development of a rapid glycosylation profiling system using mass spectrometry datR01GM103547 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI DESAIRE, HEATHER R · 2012 to 2017
$1.8M
NIGMS NIH HHS R01 GM103547NIGMS NIH HHS R35 GM130354
6 · The paper itself

Abstract

"The totality is not, as it were, a mere heap, but the whole is something besides the parts."-Aristotle. We built a classifier that uses the totality of the glycomic profile, not restricted to a few glycoforms, to differentiate samples from two different sources. This approach, which relies on using thousands of features, is a radical departure from current strategies, where most of the glycomic profile is ignored in favor of selecting a few features, or even a single feature, meant to capture the differences in sample types. The classifier can be used to differentiate the source of the material; applicable sources may be different species of animals, different protein production methods, or, most importantly, different biological states (disease vs healthy). The classifier can be used on glycomic data in any form, including derivatized monosaccharides, intact glycans, or glycopeptides. It takes advantage of the fact that changing the source material can cause a change in the glycomic profile in many subtle ways: some glycoforms can be upregulated, some downregulated, some may appear unchanged, yet their proportion-with respect to other forms present-can be altered to a detectable degree. By classifying samples using the entirety of their glycan abundances, along with the glycans' relative proportions to each other, the "Aristotle Classifier" is more effective at capturing the underlying trends than standard classification procedures used in glycomics, including PCA (principal components analysis). It also outperforms workflows where a single, representative glycomic-based biomarker is used to classify samples. We describe the Aristotle Classifier and provide several examples of its utility for biomarker studies and other classification problems using glycomic data from several sources.

Indexed as

BiomarkersGlycomicsGlycopeptidesGlycoproteinsGlycosylationHumansLiver CirrhosisMonosaccharidesPolysaccharidesPrincipal Component AnalysisSoftwareSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTerminology as TopicBiomarkersGlycopeptidesGlycoproteinsMonosaccharidesPolysaccharides

Identifiers

PMID31407893
PMCPMC6768561

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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.