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Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk.

Identifieur interne : 001546 ( PubMed/Corpus ); précédent : 001545; suivant : 001547

Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk.

Auteurs : Robert J. Macinnis ; Daniel F. Schmidt ; Enes Makalic ; Gianluca Severi ; Liesel M. Fitzgerald ; Matthias Reumann ; Miroslaw K. Kapuscinski ; Adam Kowalczyk ; Zeyu Zhou ; Benjamin Goudey ; Guoqi Qian ; Quang M. Bui ; Daniel J. Park ; Adam Freeman ; Melissa C. Southey ; Ali Amin Al Olama ; Zsofia Kote-Jarai ; Rosalind A. Eeles ; John L. Hopper ; Graham G. Giles

Source :

RBID : pubmed:27539266

Abstract

We have developed a genome-wide association study analysis method called DEPTH (DEPendency of association on the number of Top Hits) to identify genomic regions potentially associated with disease by considering overlapping groups of contiguous markers (e.g., SNPs) across the genome. DEPTH is a machine learning algorithm for feature ranking of ultra-high dimensional datasets, built from well-established statistical tools such as bootstrapping, penalized regression, and decision trees. Unlike marginal regression, which considers each SNP individually, the key idea behind DEPTH is to rank groups of SNPs in terms of their joint strength of association with the outcome. Our aim was to compare the performance of DEPTH with that of standard logistic regression analysis.

DOI: 10.1158/1055-9965.EPI-16-0301
PubMed: 27539266

Links to Exploration step

pubmed:27539266

Le document en format XML

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<name sortKey="Zhou, Zeyu" sort="Zhou, Zeyu" uniqKey="Zhou Z" first="Zeyu" last="Zhou">Zeyu Zhou</name>
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<name sortKey="Freeman, Adam" sort="Freeman, Adam" uniqKey="Freeman A" first="Adam" last="Freeman">Adam Freeman</name>
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<name sortKey="Al Olama, Ali Amin" sort="Al Olama, Ali Amin" uniqKey="Al Olama A" first="Ali Amin" last="Al Olama">Ali Amin Al Olama</name>
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<nlm:affiliation>Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.</nlm:affiliation>
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<name sortKey="Kote Jarai, Zsofia" sort="Kote Jarai, Zsofia" uniqKey="Kote Jarai Z" first="Zsofia" last="Kote-Jarai">Zsofia Kote-Jarai</name>
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<name sortKey="Eeles, Rosalind A" sort="Eeles, Rosalind A" uniqKey="Eeles R" first="Rosalind A" last="Eeles">Rosalind A. Eeles</name>
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<div type="abstract" xml:lang="en">We have developed a genome-wide association study analysis method called DEPTH (DEPendency of association on the number of Top Hits) to identify genomic regions potentially associated with disease by considering overlapping groups of contiguous markers (e.g., SNPs) across the genome. DEPTH is a machine learning algorithm for feature ranking of ultra-high dimensional datasets, built from well-established statistical tools such as bootstrapping, penalized regression, and decision trees. Unlike marginal regression, which considers each SNP individually, the key idea behind DEPTH is to rank groups of SNPs in terms of their joint strength of association with the outcome. Our aim was to compare the performance of DEPTH with that of standard logistic regression analysis.</div>
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<Year>2016</Year>
<Month>08</Month>
<Day>19</Day>
</DateCreated>
<DateRevised>
<Year>2017</Year>
<Month>06</Month>
<Day>01</Day>
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<ISSN IssnType="Electronic">1538-7755</ISSN>
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<Volume>25</Volume>
<Issue>12</Issue>
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<Year>2016</Year>
<Month>Dec</Month>
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<Title>Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology</Title>
<ISOAbbreviation>Cancer Epidemiol. Biomarkers Prev.</ISOAbbreviation>
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<ArticleTitle>Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk.</ArticleTitle>
<Pagination>
<MedlinePgn>1619-1624</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">We have developed a genome-wide association study analysis method called DEPTH (DEPendency of association on the number of Top Hits) to identify genomic regions potentially associated with disease by considering overlapping groups of contiguous markers (e.g., SNPs) across the genome. DEPTH is a machine learning algorithm for feature ranking of ultra-high dimensional datasets, built from well-established statistical tools such as bootstrapping, penalized regression, and decision trees. Unlike marginal regression, which considers each SNP individually, the key idea behind DEPTH is to rank groups of SNPs in terms of their joint strength of association with the outcome. Our aim was to compare the performance of DEPTH with that of standard logistic regression analysis.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We selected 1,854 prostate cancer cases and 1,894 controls from the UK for whom 541,129 SNPs were measured using the Illumina Infinium HumanHap550 array. Confirmation was sought using 4,152 cases and 2,874 controls, ascertained from the UK and Australia, for whom 211,155 SNPs were measured using the iCOGS Illumina Infinium array.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">From the DEPTH analysis, we identified 14 regions associated with prostate cancer risk that had been reported previously, five of which would not have been identified by conventional logistic regression. We also identified 112 novel putative susceptibility regions.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">DEPTH can reveal new risk-associated regions that would not have been identified using a conventional logistic regression analysis of individual SNPs.</AbstractText>
<AbstractText Label="IMPACT" NlmCategory="CONCLUSIONS">This study demonstrates that the DEPTH algorithm could identify additional genetic susceptibility regions that merit further investigation. Cancer Epidemiol Biomarkers Prev; 25(12); 1619-24. ©2016 AACR.</AbstractText>
<CopyrightInformation>©2016 American Association for Cancer Research.</CopyrightInformation>
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<Affiliation>Université Paris-Saclay, Univ. Paris-Sud, UVSQ, CESP, INSERM, Villejuif, France.</Affiliation>
</AffiliationInfo>
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<Affiliation>Gustave Roussy, F-94805, Villejuif, France.</Affiliation>
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<Affiliation>Melbourne Bioinformatics Platform, Victorian Life Sciences Computation Initiative, University of Melbourne, Victoria, Australia.</Affiliation>
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<Affiliation>The Institute of Cancer Research, London, United Kingdom.</Affiliation>
</AffiliationInfo>
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<ForeName>Rosalind A</ForeName>
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<Affiliation>Department of Epidemiology, School of Public Health and Institute of Health and Environment, Seoul National University, Seoul, South Korea.</Affiliation>
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