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How do I obtain and analyze data from The Cancer Genome Atlas (TCGA)? Which TCGA datasets have specific mutations in my gene of interest?
This recipe provides a method for identifying and obtaining specific datasets of interest from The Cancer Genome Atlas (TCGA), through a web-based tool called FireBrowse. An example use of this recipe is a case where an investigator may have a gene they are interested in, such as ERCC2, and would like to know if there are mutations in this gene in specific datasets of interest, such as bladder cancer.
Tumors arise from mutational changes to healthy cells, and are frequently deficient in one or more DNA repair pathways. The accumulation of mutations in tumor can be described by the “mutational signature”, a pattern of genetic mutations found in tumor DNA, which reflect different mutation events. Mutational signatures can be specific to certain tissues or cancer types. Many of these mutational signatures are associated with DNA repair pathways.
An in-depth study of urothelial carcinoma, which causes ~150,000 deaths annually, by Kim et al. (Nature Genetics, 2016) has identified a mutational signature in bladder cancer involving the nucleotide-excision repair (NER) pathway. Kim et al. identified a mutational signature involving ERCC2, a gene encoding a DNA helicase which plays a critical role in the NER pathway. Somatic mutations in this gene may prevent proper functioning of the NER pathway, allowing mutations to accumulate. Uniquely, urothelial cancer is the only known tumor type to date in which ERCC2 is significantly mutated.
Kim et al. used the collection of bladder carcinoma (BLCA) samples in The Cancer Genome Atlas (TCGA) to complete their analysis. Data were downloaded from the Broad Institute TCGA Genome Data Analysis Center, and samples were categorized based on mutational status. Tumors with somatic, missense mutations in ERCC2 were compared to non-mutated (wild-type) samples to identify the comprehensive mutational landscape of bladder cancer (also described in this TCGA paper).
This recipe provides a method for processing data from The Cancer Genome Atlas (TCGA), to identify samples which have mutations in specific genes. The purpose of this recipe is to categorize data by mutational status, for further downstream analysis (e.g. comparing tumors of different mutational status, etc.). Data is collected from FireBrowse; Galaxy and GenePattern are used to categorize samples by mutational status and generate GCT and CLS files. The RNA-seq datasets are gene-level normalized RSEM expression estimates.
The Cancer Genome Atlas labels its datasets with the TCGA barcode, an identifer that describes the metadata associated with sample. You can learn more about the TCGA Barcodes on the NIH National Cancer Institute Wiki page (see also: working with TCGA data).
TCGA barcodes adhere to a certain format:
TCGA-00-1111-22A-33B-4444-55. For this recipe, we are interested in the Sample type, indicated by the
22A section of the barcode. For this recipe we are interested in samples with designation
01 (solid tumor, or TP) or
11 (solid tissue normal, or NT), which are paired tumor-normal samples.