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TumorFusions: an integrative resource for cancer-associated transcript fusions

机译:TumorFusions:与癌症相关的转录本融合的整合资源

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摘要

Gene fusion represents a class of molecular aberrations in cancer and has been exploited for therapeutic purposes. In this paper we describe TumorFusions, a data portal that catalogues 20 731 gene fusions detected in 9966 well characterized cancer samples and 648 normal specimens from The Cancer Genome Atlas (TCGA). The portal spans 33 cancer types in TCGA. Fusion transcripts were identified via a uniform pipeline, including filtering against a list of 3838 transcript fusions detected in a panel of 648 non-neoplastic samples. Fusions were mapped to somatic DNA rearrangements identified using whole genome sequencing data from 561 cancer samples as a means of validation. We observed that 65% of transcript fusions were associated with a chromosomal alteration, which is annotated in the portal. Other features of the portal include links to SNP array-based copy number levels and mutational patterns, exon and transcript level expressions of the partner genes, and a network-based centrality score for prioritizing functional fusions. Our portal aims to be a broadly applicable and user friendly resource for cancer gene annotation and is publicly available at .
机译:基因融合代表癌症中的一类分子畸变,已被用于治疗目的。在本文中,我们描述了TumorFusions,这是一个数据门户网站,其中列出了在9966个特征明确的癌症样本和648个正常样本(癌症基因组图谱)中检测到的20731种基因融合。该门户网站涵盖TCGA中的33种癌症类型。融合转录本通过统一的管道进行鉴定,包括针对在648个非肿瘤样本中检测到的3838个转录本融合进行过滤。使用来自561个癌症样品的全基因组测序数据将融合体定位到鉴定的体细胞DNA重排,作为验证的手段。我们观察到转录融合物中有65%与染色体改变有关,该改变在门户中有注释。该门户网站的其他功能包括指向基于SNP阵列的拷贝数水平和突变模式,伴侣基因的外显子和转录水平表达的链接,以及基于网络的集中度评分,用于优先进行功能融合。我们的门户网站旨在成为癌症基因注释的广泛适用且用户友好的资源,可在上公开获取。

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