{"title":"确定条件特异性基因共表达网络。","authors":"Vikram Kalluru, Raghu Machiraju, Kun Huang","doi":"10.1504/IJCBDD.2013.052201","DOIUrl":null,"url":null,"abstract":"<p><p>Since co-expressed genes often are co-regulated by a group of transcription factors, different conditions (e.g. disease versus normal) may lead to different transcription factor activities and therefore different co-expression networks. We propose a method for identifying condition-specific co-expression networks by combining our recently developed network quasi-clique mining algorithm and the expected conditional F-statistic. We apply this method to compare the transcriptional programmes between the non-basal and basal types of breast cancers. The results provide a new perspective for studying gene interaction dynamics in cancers and assessing the effects of perturbation on key genes such as transcription factors. Our work is a way for dynamically characterising the gene interaction networks.</p>","PeriodicalId":39227,"journal":{"name":"International Journal of Computational Biology and Drug Design","volume":" ","pages":"50-9"},"PeriodicalIF":0.0000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1504/IJCBDD.2013.052201","citationCount":"3","resultStr":"{\"title\":\"Identify condition-specific gene co-expression networks.\",\"authors\":\"Vikram Kalluru, Raghu Machiraju, Kun Huang\",\"doi\":\"10.1504/IJCBDD.2013.052201\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Since co-expressed genes often are co-regulated by a group of transcription factors, different conditions (e.g. disease versus normal) may lead to different transcription factor activities and therefore different co-expression networks. We propose a method for identifying condition-specific co-expression networks by combining our recently developed network quasi-clique mining algorithm and the expected conditional F-statistic. We apply this method to compare the transcriptional programmes between the non-basal and basal types of breast cancers. The results provide a new perspective for studying gene interaction dynamics in cancers and assessing the effects of perturbation on key genes such as transcription factors. Our work is a way for dynamically characterising the gene interaction networks.</p>\",\"PeriodicalId\":39227,\"journal\":{\"name\":\"International Journal of Computational Biology and Drug Design\",\"volume\":\" \",\"pages\":\"50-9\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1504/IJCBDD.2013.052201\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Computational Biology and Drug Design\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1504/IJCBDD.2013.052201\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2013/2/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Computational Biology and Drug Design","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1504/IJCBDD.2013.052201","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/2/21 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
Since co-expressed genes often are co-regulated by a group of transcription factors, different conditions (e.g. disease versus normal) may lead to different transcription factor activities and therefore different co-expression networks. We propose a method for identifying condition-specific co-expression networks by combining our recently developed network quasi-clique mining algorithm and the expected conditional F-statistic. We apply this method to compare the transcriptional programmes between the non-basal and basal types of breast cancers. The results provide a new perspective for studying gene interaction dynamics in cancers and assessing the effects of perturbation on key genes such as transcription factors. Our work is a way for dynamically characterising the gene interaction networks.