<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(2)</volume><submitter>Wang Y</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To identify the molecular background of eyelid sebaceous gland carcinomas (SCs), we conducted the integrated whole-exome sequencing and transcriptome sequencing for eyelid SCs in this study.&lt;h4>Methods&lt;/h4>The genetic alterations were studied by whole-exome sequencing, and the messenger RNA expression was studied using Oxford Nanopore Technologies (ONT) in five paired fresh eyelid SC tissues and adjacent normal tissues. Integrated analysis of exome and transcriptomic information was conducted for filtering candidate driver genes. Protein-protein interaction (PPI) network of filtered candidate genes was analyzed by STRING. The protein expression was verified by immunohistochemistry in 29 eyelid SCs and 17 compared normal sebaceous gland tissues.&lt;h4>Results&lt;/h4>The average nu</pubmed_abstract><journal>Translational vision science &amp; technology</journal><pagination>4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9907373</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Integrated Whole-Exome and Transcriptome Sequencing Indicated Dysregulation of Cholesterol Metabolism in Eyelid Sebaceous Gland Carcinoma.</pubmed_title><pmcid>PMC9907373</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Hao P</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Han R</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Integrated Whole-Exome and Transcriptome Sequencing Indicated Dysregulation of Cholesterol Metabolism in Eyelid Sebaceous Gland Carcinoma.</name><description>&lt;h4>Purpose&lt;/h4>To identify the molecular background of eyelid sebaceous gland carcinomas (SCs), we conducted the integrated whole-exome sequencing and transcriptome sequencing for eyelid SCs in this study.&lt;h4>Methods&lt;/h4>The genetic alterations were studied by whole-exome sequencing, and the messenger RNA expression was studied using Oxford Nanopore Technologies (ONT) in five paired fresh eyelid SC tissues and adjacent normal tissues. Integrated analysis of exome and transcriptomic information was conducted for filtering candidate driver genes. Protein-protein interaction (PPI) network of filtered candidate genes was analyzed by STRING. The protein expression was verified by immunohistochemistry in 29 eyelid SCs and 17 compared normal sebaceous gland tissues.&lt;h4>Results&lt;/h4>The average nu</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-07-14T20:16:03.733Z</modification><creation>2025-04-04T08:34:58.275Z</creation></dates><accession>S-EPMC9907373</accession><cross_references><pubmed>36735267</pubmed><doi>10.1167/tvst.12.2.4</doi></cross_references></HashMap>