{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,22]],"date-time":"2025-02-22T00:45:05Z","timestamp":1740185105529,"version":"3.37.3"},"reference-count":7,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2017,9,29]],"date-time":"2017-09-29T00:00:00Z","timestamp":1506643200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/about_us\/legal\/notices"}],"funder":[{"DOI":"10.13039\/501100003725","name":"National Research Foundation of Korea","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100003725","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100007431","name":"NRF","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100007431","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2018,2,1]]},"abstract":"Abstract<\/jats:title>\n \n Summary<\/jats:title>\n Whole-exome sequencing (WES) data have been used for identifying copy number aberrations in cancer cells. Nonetheless, the use of WES is still challenging for identification of focal aberrant regions in multiple samples that may contain cancer driver genes. In this study, we developed a wavelet-based method for identifying focal genomic aberrant regions in the WES data from cancer cells (WIFA-X). When we applied WIFA-X to glioblastoma multiforme and lung adenocarcinoma datasets, WIFA-X outperformed other approaches on identifying cancer driver genes.<\/jats:p>\n <\/jats:sec>\n \n Availability and implementation<\/jats:title>\n R source code is available at http:\/\/gcancer.org\/wifax.<\/jats:p>\n <\/jats:sec>\n \n Supplementary information<\/jats:title>\n Supplementary data are available at Bioinformatics online.<\/jats:p>\n <\/jats:sec>","DOI":"10.1093\/bioinformatics\/btx620","type":"journal-article","created":{"date-parts":[[2017,9,27]],"date-time":"2017-09-27T11:10:10Z","timestamp":1506510610000},"page":"519-521","source":"Crossref","is-referenced-by-count":2,"title":["Identification of cancer driver genes in focal genomic aberrations from whole-exome sequencing data"],"prefix":"10.1093","volume":"34","author":[{"given":"Ho","family":"Jang","sequence":"first","affiliation":[{"name":"School of Electrical Engineering and Computer Science, Gwangju Institute of Science and Technology, Gwangju, South Korea"}]},{"given":"Hyunju","family":"Lee","sequence":"additional","affiliation":[{"name":"School of Electrical Engineering and Computer Science, Gwangju Institute of Science and Technology, Gwangju, South Korea"}]}],"member":"286","published-online":{"date-parts":[[2017,10,3]]},"reference":[{"key":"2023012712322053700_btx620-B1","first-page":"2), S2.","article-title":"Convex: copy number variation estimation in exome sequencing data using hmm","volume":"14","author":"Amarasinghe","year":"2013","journal-title":"BMC Bioinformatics"},{"key":"2023012712322053700_btx620-B2","doi-asserted-by":"crossref","first-page":"20007","DOI":"10.1073\/pnas.0710052104","article-title":"Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma","volume":"104","author":"Beroukhim","year":"2007","journal-title":"Proc. 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