Movement Disorders (revue)

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Applying Bioinformatics to Proteomics: Is Machine Learning the Answer to Biomarker Discovery for PD and MSA?

Identifieur interne : 001208 ( Main/Exploration ); précédent : 001207; suivant : 001209

Applying Bioinformatics to Proteomics: Is Machine Learning the Answer to Biomarker Discovery for PD and MSA?

Auteurs : Hayley A. Mattison [États-Unis] ; Tessandra Stewart [États-Unis] ; JING ZHANG [États-Unis]

Source :

RBID : Pascal:13-0017915

Descripteurs français

English descriptors

Abstract

Bioinformatics tools are increasingly being applied to proteomic data to facilitate the identification of biomarkers and classification of patients. In the June, 2012 issue, Ishigami et al. used principal component analysis (PCA) to extract features and support vector machine (SVM) to differentiate and classify cerebrospinal fluid (CSF) samples from two small cohorts of patients diagnosed with either Parkinson's disease (PD) or multiple system atrophy (MSA) based on differences in the patterns of peaks generated with matrix-assisted desorption/ ionization time-of-flight mass spectrometry (MALDI-TOF MS). PCA accurately segregated patients with PD and MSA from controls when the cohorts were combined, but did not perform well when segregating PD from MSA. On the other hand, SVM, a machine learning classification model, correctly classified the samples from patients with early PD or MSA, and the peak at m/z 6250 was identified as a strong contributor to the ability of SVM to distinguish the proteomic profiles of either cohort when trained on one cohort. This study, while preliminary, provides promising results for the application of bioinformatics tools to proteomic data, an approach that may eventually facilitate the ability of clinicians to differentiate and diagnose closely related parkinsonian disorders.


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">Applying Bioinformatics to Proteomics: Is Machine Learning the Answer to Biomarker Discovery for PD and MSA?</title>
<author>
<name sortKey="Mattison, Hayley A" sort="Mattison, Hayley A" uniqKey="Mattison H" first="Hayley A." last="Mattison">Hayley A. Mattison</name>
<affiliation wicri:level="4">
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Washington</s1>
<s2>Seattle, Washington</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName>
<region type="state">Washington (État)</region>
<settlement type="city">Seattle</settlement>
</placeName>
<orgName type="university">Université de Washington</orgName>
</affiliation>
</author>
<author>
<name sortKey="Stewart, Tessandra" sort="Stewart, Tessandra" uniqKey="Stewart T" first="Tessandra" last="Stewart">Tessandra Stewart</name>
<affiliation wicri:level="4">
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Washington</s1>
<s2>Seattle, Washington</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName>
<region type="state">Washington (État)</region>
<settlement type="city">Seattle</settlement>
</placeName>
<orgName type="university">Université de Washington</orgName>
</affiliation>
</author>
<author>
<name sortKey="Jing Zhang" sort="Jing Zhang" uniqKey="Jing Zhang" last="Jing Zhang">JING ZHANG</name>
<affiliation wicri:level="4">
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Washington</s1>
<s2>Seattle, Washington</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName>
<region type="state">Washington (État)</region>
<settlement type="city">Seattle</settlement>
</placeName>
<orgName type="university">Université de Washington</orgName>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">13-0017915</idno>
<date when="2012">2012</date>
<idno type="stanalyst">PASCAL 13-0017915 INIST</idno>
<idno type="RBID">Pascal:13-0017915</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000047</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002C67</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000281</idno>
<idno type="wicri:doubleKey">0885-3185:2012:Mattison H:applying:bioinformatics:to</idno>
<idno type="wicri:Area/Main/Merge">001260</idno>
<idno type="wicri:Area/Main/Curation">001208</idno>
<idno type="wicri:Area/Main/Exploration">001208</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">Applying Bioinformatics to Proteomics: Is Machine Learning the Answer to Biomarker Discovery for PD and MSA?</title>
<author>
<name sortKey="Mattison, Hayley A" sort="Mattison, Hayley A" uniqKey="Mattison H" first="Hayley A." last="Mattison">Hayley A. Mattison</name>
<affiliation wicri:level="4">
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Washington</s1>
<s2>Seattle, Washington</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName>
<region type="state">Washington (État)</region>
<settlement type="city">Seattle</settlement>
</placeName>
<orgName type="university">Université de Washington</orgName>
</affiliation>
</author>
<author>
<name sortKey="Stewart, Tessandra" sort="Stewart, Tessandra" uniqKey="Stewart T" first="Tessandra" last="Stewart">Tessandra Stewart</name>
<affiliation wicri:level="4">
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Washington</s1>
<s2>Seattle, Washington</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName>
<region type="state">Washington (État)</region>
<settlement type="city">Seattle</settlement>
</placeName>
<orgName type="university">Université de Washington</orgName>
</affiliation>
</author>
<author>
<name sortKey="Jing Zhang" sort="Jing Zhang" uniqKey="Jing Zhang" last="Jing Zhang">JING ZHANG</name>
<affiliation wicri:level="4">
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Washington</s1>
<s2>Seattle, Washington</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName>
<region type="state">Washington (État)</region>
<settlement type="city">Seattle</settlement>
</placeName>
<orgName type="university">Université de Washington</orgName>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint>
<date when="2012">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Discoveries</term>
<term>Learning</term>
<term>Mass spectrometry</term>
<term>Multiple system atrophy</term>
<term>Nervous system diseases</term>
<term>Parkinson disease</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Maladie de Parkinson</term>
<term>Atrophie multisystématisée</term>
<term>Pathologie du système nerveux</term>
<term>Apprentissage</term>
<term>Découverte</term>
<term>Spectrométrie masse</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Bioinformatics tools are increasingly being applied to proteomic data to facilitate the identification of biomarkers and classification of patients. In the June, 2012 issue, Ishigami et al. used principal component analysis (PCA) to extract features and support vector machine (SVM) to differentiate and classify cerebrospinal fluid (CSF) samples from two small cohorts of patients diagnosed with either Parkinson's disease (PD) or multiple system atrophy (MSA) based on differences in the patterns of peaks generated with matrix-assisted desorption/ ionization time-of-flight mass spectrometry (MALDI-TOF MS). PCA accurately segregated patients with PD and MSA from controls when the cohorts were combined, but did not perform well when segregating PD from MSA. On the other hand, SVM, a machine learning classification model, correctly classified the samples from patients with early PD or MSA, and the peak at m/z 6250 was identified as a strong contributor to the ability of SVM to distinguish the proteomic profiles of either cohort when trained on one cohort. This study, while preliminary, provides promising results for the application of bioinformatics tools to proteomic data, an approach that may eventually facilitate the ability of clinicians to differentiate and diagnose closely related parkinsonian disorders.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Washington (État)</li>
</region>
<settlement>
<li>Seattle</li>
</settlement>
<orgName>
<li>Université de Washington</li>
</orgName>
</list>
<tree>
<country name="États-Unis">
<region name="Washington (État)">
<name sortKey="Mattison, Hayley A" sort="Mattison, Hayley A" uniqKey="Mattison H" first="Hayley A." last="Mattison">Hayley A. Mattison</name>
</region>
<name sortKey="Jing Zhang" sort="Jing Zhang" uniqKey="Jing Zhang" last="Jing Zhang">JING ZHANG</name>
<name sortKey="Stewart, Tessandra" sort="Stewart, Tessandra" uniqKey="Stewart T" first="Tessandra" last="Stewart">Tessandra Stewart</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001208 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001208 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     Pascal:13-0017915
   |texte=   Applying Bioinformatics to Proteomics: Is Machine Learning the Answer to Biomarker Discovery for PD and MSA?
}}

Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024