Document Type
Article
Publication Date
1-4-2018
JAX Source
Nucleic Acids Res 2018 Jan 4; 46(D1):D1144-D1149
Volume
46
Issue
D1
First Page
1144
Last Page
1144
ISSN
1362-4962
PMID
29099951
DOI
https://doi.org/10.1093/nar/gkx1018
Grant
R140606, CA19012, CA198320, CA034196, CA16672, CA198320
Abstract
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 http://www.tumorfusions.org. Nucleic Acids Res 2018 Jan 4; 46(D1):D1144-D1149.
Recommended Citation
Hu X,
Wang Q,
Tang M,
Barthel F,
Amin S,
Yoshihara K,
Lang F,
Martinez-Ledesma E,
Lee S,
Zheng S,
Verhaak R.
TumorFusions: an integrative resource for cancer-associated transcript fusions. Nucleic Acids Res 2018 Jan 4; 46(D1):D1144-D1149
Comments
This article is available under the Creative Commons CC-BY-NC license