Εμφάνιση απλής εγγραφής

dc.creatorBonab R.A., Asfa S., Kontou P., Karakülah G., Pavlopoulou A.en
dc.date.accessioned2023-01-31T07:38:59Z
dc.date.available2023-01-31T07:38:59Z
dc.date.issued2022
dc.identifier10.7717/peerj.14149
dc.identifier.issn21678359
dc.identifier.urihttp://hdl.handle.net/11615/71808
dc.description.abstractMicroRNAs represent major regulatory components of the disease epigenome and they constitute powerful biomarkers for the accurate diagnosis and prognosis of various diseases, including cancers. The advent of high-throughput technologies facilitated the generation of a vast amount of miRNA-cancer association data. Computational approaches have been utilized widely to effectively analyze and interpret these data towards the identification of miRNA signatures for diverse types of cancers. Herein, a novel computational workflow was applied to discover core sets of miRNA interactions for the major groups of neoplastic diseases by employing network-based methods. To this end, miRNA-cancer association data from four comprehensive publicly available resources were utilized for constructing miRNA-centered networks for each major group of neoplasms. The corresponding miRNA-miRNA interactions were inferred based on shared functionally related target genes. The topological attributes of the generated networks were investigated in order to detect clusters of highly interconnected miRNAs that form core modules in each network. Those modules that exhibited the highest degree of mutual exclusivity were selected from each graph. In this way, neoplasm-specific miRNA modules were identified that could represent potential signatures for the corresponding diseases. Copyright 2022 Arshinchi Bonab et al.en
dc.language.isoenen
dc.sourcePeerJen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85140408854&doi=10.7717%2fpeerj.14149&partnerID=40&md5=9eb6e3d5664fc26d04dd223901f23cb3
dc.subjectmicroRNAen
dc.subjectmicrorna 1296 3pen
dc.subjectmicrorna 3689en
dc.subjectmicrorna 3689cen
dc.subjectmicrorna 3689een
dc.subjectmicrorna 4273en
dc.subjectmicrorna 4422en
dc.subjectmicrorna 4432en
dc.subjectmicrorna 4445 3pen
dc.subjectmicrorna 4694 3pen
dc.subjectmicrorna 4720en
dc.subjectmicrorna 5002en
dc.subjectmicrorna 5002 3pen
dc.subjectmicrorna 5011 3pen
dc.subjectmicrorna 522 2pen
dc.subjectmicrorna 548ae 5pen
dc.subjectmicrorna 548alen
dc.subjectmicrorna 548ao 5pen
dc.subjectmicrorna 5688en
dc.subjectmicrorna 5699en
dc.subjectmicrorna 5699 5pen
dc.subjectmicrorna 5702en
dc.subjectmicrorna 6511b 5pen
dc.subjectmicrorna 6719 3pen
dc.subjectmicrorna 6724 5pen
dc.subjectmicrorna 6748 5pen
dc.subjectmicrorna 6753 3pen
dc.subjectmicrorna 6770 5pen
dc.subjectmicrorna 6773 5pen
dc.subjectmicrorna 6811 5pen
dc.subjectmicrorna 6828 3pen
dc.subjectmicrorna 7107 3pen
dc.subjectmicrorna 7154 5pen
dc.subjectmicrorna 7515en
dc.subjectmicrorna 8062en
dc.subjectmicrorna 8067en
dc.subjectmicrorna 8068en
dc.subjectsmall untranslated RNAen
dc.subjectunclassified drugen
dc.subjectadenoid cystic carcinomaen
dc.subjectArticleen
dc.subjectbioinformaticsen
dc.subjectbladder canceren
dc.subjectbrain canceren
dc.subjectcancer prognosisen
dc.subjectcolorectal canceren
dc.subjectepigenomeen
dc.subjectgene ontologyen
dc.subjecthead and neck canceren
dc.subjecthumanen
dc.subjectlung adenocarcinomaen
dc.subjectlung canceren
dc.subjectneoplasmen
dc.subjectnetwork analysisen
dc.subjectnomenclatureen
dc.subjectovary canceren
dc.subjectprotein localizationen
dc.subjectprotein RNA bindingen
dc.subjectskin canceren
dc.subjectsquamous cell carcinomaen
dc.subjectstomach tumoren
dc.subjectsystems biologyen
dc.subjecttestis tumoren
dc.subjectthyroid follicular carcinomaen
dc.subjectPeerJ Inc.en
dc.titleIdentification of neoplasm-specific signatures of miRNA interactions by employing a systems biology approachen
dc.typejournalArticleen


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