<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Liu M</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Sepsis is a life-threatening disease causing millions of deaths every year. It has been reported that programmed cell death (PCD) plays a critical role in the development and progression of sepsis, which has the potential to be a diagnosis and prognosis indicator for patient with sepsis.&lt;h4>Methods&lt;/h4>Fourteen PCD patterns were analyzed for model construction. Seven transcriptome datasets and a single cell sequencing dataset were collected from the Gene Expression Omnibus database.&lt;h4>Results&lt;/h4>A total of 289 PCD-related differentially expressed genes were identified between sepsis patients and healthy individuals. The machine learning algorithm screened three PCD-related genes, NLRC4, TXN and S100A9, as potential biomarkers for sepsis. The area under curve of the dia</pubmed_abstract><journal>PeerJ</journal><pagination>e19077</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11871900</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Leveraging diverse cell-death patterns in diagnosis of sepsis by integrating bioinformatics and machine learning.</pubmed_title><pmcid>PMC11871900</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Sheng Y</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Zhu R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Leveraging diverse cell-death patterns in diagnosis of sepsis by integrating bioinformatics and machine learning.</name><description>&lt;h4>Background&lt;/h4>Sepsis is a life-threatening disease causing millions of deaths every year. It has been reported that programmed cell death (PCD) plays a critical role in the development and progression of sepsis, which has the potential to be a diagnosis and prognosis indicator for patient with sepsis.&lt;h4>Methods&lt;/h4>Fourteen PCD patterns were analyzed for model construction. Seven transcriptome datasets and a single cell sequencing dataset were collected from the Gene Expression Omnibus database.&lt;h4>Results&lt;/h4>A total of 289 PCD-related differentially expressed genes were identified between sepsis patients and healthy individuals. The machine learning algorithm screened three PCD-related genes, NLRC4, TXN and S100A9, as potential biomarkers for sepsis. The area under curve of the dia</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-02T19:15:27.099Z</modification><creation>2025-04-04T02:47:46.621Z</creation></dates><accession>S-EPMC11871900</accession><cross_references><pubmed>40028203</pubmed><doi>10.7717/peerj.19077</doi></cross_references></HashMap>