Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.11861/7385
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dc.contributor.authorWu, Qiongen_US
dc.contributor.authorZheng, Xubinen_US
dc.contributor.authorProf. LEUNG Kwong Saken_US
dc.contributor.authorWong, Man-Honen_US
dc.contributor.authorTsui, Stephen, Kwok-Wingen_US
dc.contributor.authorCheng, Lixinen_US
dc.date.accessioned2023-02-20T09:00:32Z-
dc.date.available2023-02-20T09:00:32Z-
dc.date.issued2022-
dc.identifier.citationBioinformatics, July 2022, vol. 38 (14), pp. 3513–3522.en_US
dc.identifier.issn1367-4811-
dc.identifier.urihttp://hdl.handle.net/20.500.11861/7385-
dc.description.abstractMotivation Hepatocellular carcinoma (HCC) is a primary malignancy with a poor prognosis. Recently, multi-omics molecular-level measurement enables HCC diagnosis and prognosis prediction, which is crucial for early intervention of personalized therapy to diminish mortality. Here, we introduce a novel strategy utilizing DNA methylation and RNA expression data to achieve a multi-omics gene pair signature (GPS) for HCC discrimination. Results The immune genes with negative correlations between expression and promoter methylation are enriched in the highly connected cancer-related pathway network, which are considered as the candidates for HCC detection. After that, we separately construct a methylation GPS (mGPS) and an expression GPS (eGPS), and then assemble them as a meGPS with five gene pairs, in which the significant methylation and expression changes occur between HCC tumor and non-tumor groups. Reliable performance has been validated by independent tissue (age, gender and etiology) and blood datasets. This study proposes a procedure for multi-omics GPS identification and develops a novel HCC signature using both methylome and transcriptome data, suggesting potential molecular targets for the detection and therapy of HCC.en_US
dc.language.isoenen_US
dc.relation.ispartofBioinformaticsen_US
dc.titlemeGPS: a multi-omics signature for hepatocellular carcinoma detection integrating methylome and transcriptome dataen_US
dc.typePeer Reviewed Journal Articleen_US
dc.identifier.doi10.1093/bioinformatics/btac379-
item.fulltextNo Fulltext-
crisitem.author.deptDepartment of Applied Data Science-
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