DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ju, Young Seok | ko |
dc.date.accessioned | 2021-05-11T02:50:05Z | - |
dc.date.available | 2021-05-11T02:50:05Z | - |
dc.date.created | 2021-05-11 | - |
dc.date.created | 2021-05-11 | - |
dc.date.issued | 2021-04 | - |
dc.identifier.citation | CANCER CELL, v.39, no.4, pp.463 - 465 | - |
dc.identifier.issn | 1535-6108 | - |
dc.identifier.uri | http://hdl.handle.net/10203/282874 | - |
dc.description.abstract | Using sophisticated statistical analyses on population-scale cancer whole-genome sequences, a new study published in Cell characterizes the genomic architecture of intratumor heterogeneity (ITH). It results in an unprecedented snapshot of subclones in about 30 cancer types, generating a wealth of insight into the underlying mutational events, processes, and their selection. | - |
dc.language | English | - |
dc.publisher | CELL PRESS | - |
dc.title | A large-scale snapshot of intratumor heterogeneity in human cancer | - |
dc.type | Article | - |
dc.identifier.wosid | 000640027300008 | - |
dc.identifier.scopusid | 2-s2.0-85103706546 | - |
dc.type.rims | ART | - |
dc.citation.volume | 39 | - |
dc.citation.issue | 4 | - |
dc.citation.beginningpage | 463 | - |
dc.citation.endingpage | 465 | - |
dc.citation.publicationname | CANCER CELL | - |
dc.identifier.doi | 10.1016/j.ccell.2021.03.005 | - |
dc.contributor.localauthor | Ju, Young Seok | - |
dc.description.isOpenAccess | N | - |
dc.type.journalArticle | Editorial Material | - |
dc.subject.keywordPlus | EVOLUTIONARY HISTORY | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.