LuxHMM : DNA methylation analysis with genome segmentation via hidden Markov model

dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorMalonzo, Maia H.
dc.contributor.authorLähdesmäki, Harri
dc.contributor.departmentDepartment of Computer Scienceen
dc.contributor.groupauthorProfessorship Lähdesmäki Harrien
dc.contributor.groupauthorHelsinki Institute for Information Technology (HIIT)en
dc.contributor.groupauthorComputer Science Professorsen
dc.contributor.groupauthorComputer Science - Artificial Intelligence and Machine Learning (AIML) - Research areaen
dc.contributor.groupauthorComputer Science - Computational Life Sciences (CSLife) - Research areaen
dc.date.accessioned2023-03-22T07:53:19Z
dc.date.available2023-03-22T07:53:19Z
dc.date.issued2023-12
dc.descriptionFunding Information: This work was supported by the Ella and Georg Ehrnrooth Foundation and the Academy of Finland (grant number 314445). The funding body played no role in the design of the study, the collection, analysis, interpretation of data, or in writing the manuscript. Publisher Copyright: © 2023, The Author(s).
dc.description.abstractBackground: DNA methylation plays an important role in studying the epigenetics of various biological processes including many diseases. Although differential methylation of individual cytosines can be informative, given that methylation of neighboring CpGs are typically correlated, analysis of differentially methylated regions is often of more interest. Results: We have developed a probabilistic method and software, LuxHMM, that uses hidden Markov model (HMM) to segment the genome into regions and a Bayesian regression model, which allows handling of multiple covariates, to infer differential methylation of regions. Moreover, our model includes experimental parameters that describe the underlying biochemistry in bisulfite sequencing and model inference is done using either variational inference for efficient genome-scale analysis or Hamiltonian Monte Carlo (HMC). Conclusions: Analyses of real and simulated bisulfite sequencing data demonstrate the competitive performance of LuxHMM compared with other published differential methylation analysis methods.en
dc.description.versionPeer revieweden
dc.format.mimetypeapplication/pdf
dc.identifier.citationMalonzo, M H & Lähdesmäki, H 2023, 'LuxHMM : DNA methylation analysis with genome segmentation via hidden Markov model', BMC Bioinformatics, vol. 24, no. 1, 58. https://doi.org/10.1186/s12859-023-05174-7en
dc.identifier.doi10.1186/s12859-023-05174-7
dc.identifier.issn1471-2105
dc.identifier.otherPURE UUID: 3086a12f-5528-4bb6-9809-2256f032e45f
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/3086a12f-5528-4bb6-9809-2256f032e45f
dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/103299285/SCI_Malonzo_etal_BMC_Bioinformatics_2023.pdf
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/120156
dc.identifier.urnURN:NBN:fi:aalto-202303222481
dc.language.isoenen
dc.publisherBioMed Central
dc.relation.fundinginfoThis work was supported by the Ella and Georg Ehrnrooth Foundation and the Academy of Finland (grant number 314445). The funding body played no role in the design of the study, the collection, analysis, interpretation of data, or in writing the manuscript.
dc.relation.ispartofseriesBMC Bioinformaticsen
dc.relation.ispartofseriesVolume 24, issue 1en
dc.rightsopenAccessen
dc.subject.keywordBisulfite sequencing
dc.subject.keywordHMM
dc.subject.keywordMethylation
dc.subject.keywordProbabilistic
dc.titleLuxHMM : DNA methylation analysis with genome segmentation via hidden Markov modelen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi
dc.type.versionpublishedVersion

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