{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,6]],"date-time":"2026-04-06T22:05:13Z","timestamp":1775513113321,"version":"3.50.1"},"reference-count":71,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2020,8,13]],"date-time":"2020-08-13T00:00:00Z","timestamp":1597276800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,4,20]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Motivation<\/jats:title>\n                  <jats:p>Essential genes are required for the reproductive success at either cellular or organismal level. The identification of essential genes is important for understanding the core biological processes and identifying effective therapeutic drug targets. However, experimental identification of essential genes is costly, time consuming and labor intensive. Although several machine learning models have been developed to predict essential genes, these models are not readily applicable to lncRNAs. Moreover, the currently available models cannot be used to predict essential genes in a specific cancer type.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>In this study, we have developed a new machine learning approach, XGEP (eXpression-based Gene Essentiality Prediction), to predict essential genes and candidate lncRNAs in cancer cells. The novelty of XGEP lies in the utilization of relevant features derived from the TCGA transcriptome dataset through collaborative embedding. When evaluated on the pan-cancer dataset, XGEP was able to accurately predict human essential genes and achieve significantly higher performance than previous models. Notably, several candidate lncRNAs selected by XGEP are reported to promote cell proliferation and inhibit cell apoptosis. Moreover, XGEP also demonstrated superior performance on cancer-type-specific datasets to identify essential genes. The comprehensive lists of candidate essential genes in specific cancer types may be used to guide experimental characterization and facilitate the discovery of drug targets for cancer therapy.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Availability and implementation<\/jats:title>\n                  <jats:p>The source code and datasets used in this study are freely available at https:\/\/github.com\/BioDataLearning\/XGEP.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Supplementary information<\/jats:title>\n                  <jats:p>Supplementary data are available at Bioinformatics online.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1093\/bioinformatics\/btaa717","type":"journal-article","created":{"date-parts":[[2020,8,6]],"date-time":"2020-08-06T19:50:12Z","timestamp":1596743412000},"page":"396-403","source":"Crossref","is-referenced-by-count":20,"title":["Expression-based prediction of human essential genes and candidate lncRNAs in cancer cells"],"prefix":"10.1093","volume":"37","author":[{"given":"Shuzhen","family":"Kuang","sequence":"first","affiliation":[{"name":"Clemson University Department of Genetics and Biochemistry, , Clemson, SC 29634, USA"},{"name":"Clemson University Department of Biological Sciences, , Clemson, SC 29634, USA"}]},{"given":"Yanzhang","family":"Wei","sequence":"additional","affiliation":[{"name":"Clemson University Department of Biological Sciences, , Clemson, SC 29634, USA"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6316-7962","authenticated-orcid":false,"given":"Liangjiang","family":"Wang","sequence":"additional","affiliation":[{"name":"Clemson University Department of Genetics and Biochemistry, , Clemson, SC 29634, USA"},{"name":"Clemson University Center for Human Genetics, , Clemson, SC 29634, USA"}]}],"member":"286","published-online":{"date-parts":[[2020,8,13]]},"reference":[{"key":"2023051604092045700_btaa717-B1","doi-asserted-by":"crossref","first-page":"5455","DOI":"10.3390\/ijms20215455","article-title":"Targeting DNA damage response as a strategy to treat HPV infections","volume":"20","author":"Banerjee","year":"2019","journal-title":"Int. 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