Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/43313
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dc.contributor.authorGORCZAK, Katarzyna-
dc.contributor.authorBURZYKOWSKI, Tomasz-
dc.contributor.authorCLAESEN, Jurgen-
dc.date.accessioned2024-07-02T06:29:42Z-
dc.date.available2024-07-02T06:29:42Z-
dc.date.issued2024-
dc.date.submitted2024-07-02T05:47:42Z-
dc.identifier.citationCOMPUTATIONAL BIOLOGY AND CHEMISTRY, 111 (Art N° 108094)-
dc.identifier.urihttp://hdl.handle.net/1942/43313-
dc.description.abstractDNA methylation is an important epigenetic modification involved in gene regulation. Advances in the next generation sequencing technology have enabled the retrieval of DNA methylation information at single -base -resolution. However, due to the sequencing process and the limited amount of isolated DNA, DNAmethylation-data are often noisy and sparse, which complicates the identification of differentially methylated regions (DMRs), especially when few replicates are available. We present a varying -coefficient model for detecting DMRs by using single -base -resolved methylation information. The model simultaneously smooths the methylation profiles and allows detection of DMRs, while accounting for additional covariates. The proposed model takes into account possible overdispersion by using a beta -binomial distribution. The overdispersion itself can be modeled as a function of the genomic region and explanatory variables. We illustrate the properties of the proposed model by applying it to two real -life case studies.-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.rights2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).-
dc.subject.otherMethylation sequencing-
dc.subject.otherCpG site-
dc.subject.otherDifferentially methylated regions-
dc.subject.otherBeta-binomial model-
dc.subject.otherVarying-coefficient model-
dc.subject.otherSmoothing splines-
dc.titleA varying-coefficient model for the analysis of methylation sequencing data-
dc.typeJournal Contribution-
dc.identifier.volume111-
local.format.pages12-
local.bibliographicCitation.jcatA1-
dc.description.notesClaesen, J (corresponding author), Amsterdam UMC, Dept Epidemiol & Data Sci, VU Amsterdam, Postcode 1089, NL-1081 HV Amsterdam, Netherlands.-
dc.description.notesj.claesen@amsterdamumc.nl-
local.publisher.place125 London Wall, London, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnr108094-
dc.identifier.doi10.1016/j.compbiolchem.2024.108094-
dc.identifier.pmid38781748-
dc.identifier.isi001244301000001-
dc.contributor.orcidBurzykowski, Tomasz/0000-0003-3378-975X-
local.provider.typewosris-
local.description.affiliation[Gorczak, Katarzyna; Burzykowski, Tomasz; Claesen, Juergen] Hasselt Univ, Data Sci Inst, Hasselt, Belgium.-
local.description.affiliation[Gorczak, Katarzyna] Open Analyt NV, Antwerp, Belgium.-
local.description.affiliation[Burzykowski, Tomasz] Med Univ Bialystok, Dept Biostat & Med Informat, Bialystok, Poland.-
local.description.affiliation[Burzykowski, Tomasz] Int Drug Dev Inst IDDI, Ottignies, Belgium.-
local.description.affiliation[Claesen, Juergen] Amsterdam UMC, Dept Epidemiol & Data Sci, VU Amsterdam, Postcode 1089, NL-1081 HV Amsterdam, Netherlands.-
local.uhasselt.internationalyes-
item.fulltextWith Fulltext-
item.accessRightsOpen Access-
item.contributorGORCZAK, Katarzyna-
item.contributorBURZYKOWSKI, Tomasz-
item.contributorCLAESEN, Jurgen-
item.fullcitationGORCZAK, Katarzyna; BURZYKOWSKI, Tomasz & CLAESEN, Jurgen (2024) A varying-coefficient model for the analysis of methylation sequencing data. In: COMPUTATIONAL BIOLOGY AND CHEMISTRY, 111 (Art N° 108094).-
crisitem.journal.issn1476-9271-
crisitem.journal.eissn1476-928X-
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