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BreCAN-DB: a repository cum browser of personalized DNA breakpoint profiles of cancer genomes

机译:BreCAN-DB:癌症基因组的个性化DNA断点特征库和浏览器

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BreCAN-DB (http://brecandb.igib.res.in) is a repository cum browser of whole genome somatic DNA breakpoint profiles of cancer genomes, mapped at single nucleotide resolution using deep sequencing data. These breakpoints are associated with deletions, insertions, inversions, tandem duplications, translocations and a combination of these structural genomic alterations. The current release of BreCAN-DB features breakpoint profiles from 99 cancer-normal pairs, comprising five cancer types. We identified DNA breakpoints across genomes using high-coverage next-generation sequencing data obtained from TCGA and dbGaP. Further, in these cancer genomes, we methodically identified breakpoint hotspots which were significantly enriched with somatic structural alterations. To visualize the breakpoint profiles, a next-generation genome browser was integrated with BreCAN-DB. Moreover, we also included previously reported breakpoint profiles from 138 cancer-normal pairs, spanning 10 cancer types into the browser. Additionally, BreCAN-DB allows one to identify breakpoint hotspots in user uploaded data set. We have also included a functionality to query overlap of any breakpoint profile with regions of user's interest. Users can download breakpoint profiles from the database or may submit their data to be integrated in BreCAN-DB. We believe that BreCAN-DB will be useful resource for genomics scientific community and is a step towards personalized cancer genomics.
机译:BreCAN-DB(http://brecandb.igib.res.in)是癌症基因组全基因组体细胞DNA断点图谱的存储库和浏览器,使用深度测序数据以单核苷酸分辨率进行映射。这些断点与缺失,插入,倒位,串联重复,易位以及这些结构基因组改变的组合有关。 BreCAN-DB的当前版本具有来自99种正常癌症对的断点图谱,包括5种癌症类型。我们使用从TCGA和dbGaP获得的高覆盖率下一代测序数据鉴定了跨基因组的DNA断裂点。此外,在这些癌症基因组中,我们系统地确定了断点热点,这些断点热点明显富含体细胞结构改变。为了可视化断点图,将下一代基因组浏览器与BreCAN-DB集成在一起。此外,我们还包括了先前报告的138个癌症正常配对的断点概况,涵盖了浏览器中的10种癌症类型。此外,BreCAN-DB可以识别用户上载的数据集中的断点热点。我们还提供了查询任何断点配置文件与用户感兴趣区域重叠的功能。用户可以从数据库下载断点配置文件,也可以提交其数据以集成到BreCAN-DB中。我们相信,BreCAN-DB将成为基因组科学界的有用资源,并且是朝着个性化癌症基因组迈出的一步。

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