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pmid:36440267
Identification of hub genes of Parkinson's disease through bioinformatics analysis.
Yajun Yang · Yi Wang · Ce Wang · Xinjuan Xu · Cai Liu · Xintao Huang
Frontiers in neuroscience · 2022 doi:10.3389/fnins.2022.974838
Paper
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Experiment
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Data
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Analysis
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Complete file
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All the analysis was performed in R software. The expression profile data of PD (number: GSE7621) was acquired from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) associated with PD were screened by the \"Limma\" package of the R software. Key genes associated with PD were screened by the \"WGCNA\" package of the R software. Target genes were screened by merging the results of \"Limma\" and \"WGCNA.\" Enrichment analysis of target genes was performed by Gene Ontology (GO), Disease Ontology (DO), and Kyoto Enrichment of Genes and Genomes (KEGG). Machine learning algorithms were employed to screen for hub genes. Nomogram was constructed using the \"rms\" package. And the receiver operating characteristic curve (ROC) was plotted to detect and validate our prediction model sensitivity and specificity. Additional expression profile data of PD (number: GSE20141) was acquired from the GEO database to validate the nomogram. GSEA was used to determine the biological functions of the hub genes. Finally, RPL3L, PLEK2, PYCRL, CD99P1, LOC100133130, MELK, LINC01101, and DLG3-AS1 were identified as hub genes of PD. 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