Hupé P, La Rosa P, Liva S, Lair S, Servant N, Barillot E
Institut Curie, Service Bioinformatique, Paris, France.
Oncogene. 2007 Oct 11;26(46):6641-52. doi: 10.1038/sj.onc.1210488. Epub 2007 May 14.
In recent years, an increasing number of projects have investigated tumor genome structure, using microarray-based techniques like array comparative genomic hybridization (array-CGH) or single nucleotide polymorphism (SNP) arrays. The forthcoming studies have to integrate these former results and compare their findings to the existing sets of copy number data for validation. These sets also form the basis from which many comparative retrospective analyses can be carried out. Nevertheless, exploitation of this mass of data relies on a homogeneous preparation of copy number data, which will make it possible to compare them together, and their integration into a unified bioinformatics environment with ad hoc analysis tools and interfaces. To our knowledge, no such data integration has been proposed yet. Therefore the biologists and clinicians involved in cancer research urgently need such an integrative tool, which motivated us to undertake the construction of a database for array-CGH and other DNA copy number data for tumors (ACTuDB). When available, the associated clinical, transcriptome and loss of heterozygosity data were also integrated into ACTuDB. ACTuDB contains currently about 1500 genomic profiles for tumors and cell lines for the bladder, brain, breast, colon, liver, lymphoma, neuroblastoma, mouth and pancreas, together with data for replication timing experiments. The CGH array data were processed, using ad hoc algorithms (probe mapping, breakpoint detection, gain or loss status assignment and visualization) developed at Institut Curie. The database is available from http://bioinfo.curie.fr/actudb/ and can be browsed with a user-friendly interface. This database will be a useful resource for the genomic profiling of tumors, a field of highly active research. We invite research groups involved in tumor genome profiling to submit their data to ACTuDB.
近年来,越来越多的项目利用基于微阵列的技术,如阵列比较基因组杂交(array-CGH)或单核苷酸多态性(SNP)阵列,来研究肿瘤基因组结构。即将开展的研究必须整合这些先前的结果,并将其发现与现有的拷贝数数据集进行比较以进行验证。这些数据集也是许多比较性回顾分析的基础。然而,对这些大量数据的利用依赖于拷贝数数据的统一准备,这将使得能够将它们相互比较,并将它们整合到一个具有专门分析工具和界面的统一生物信息学环境中。据我们所知,尚未有人提出这样的数据整合方法。因此,参与癌症研究的生物学家和临床医生迫切需要这样一个整合工具,这促使我们着手构建一个用于肿瘤的阵列-CGH和其他DNA拷贝数数据的数据库(ACTuDB)。如有可用,相关的临床、转录组和杂合性缺失数据也被整合到ACTuDB中。ACTuDB目前包含约1500个肿瘤和细胞系的基因组图谱,涉及膀胱、脑、乳腺、结肠、肝脏、淋巴瘤、神经母细胞瘤、口腔和胰腺,以及复制时间实验的数据。CGH阵列数据使用居里研究所开发的专门算法(探针映射、断点检测、增益或缺失状态分配和可视化)进行处理。该数据库可从http://bioinfo.curie.fr/actudb/获取,并可通过用户友好的界面进行浏览。这个数据库将成为肿瘤基因组分析这一高度活跃研究领域的有用资源。我们邀请参与肿瘤基因组分析的研究小组将他们的数据提交到ACTuDB。