Mutation Analysis (MutSig v1.5)
Kidney Chromophobe (Primary solid tumor)
02 April 2015  |  analyses__2015_04_02
Maintainer Information
Citation Information
Maintained by David Heiman (Broad Institute)
Cite as Broad Institute TCGA Genome Data Analysis Center (2015): Mutation Analysis (MutSig v1.5). Broad Institute of MIT and Harvard. doi:10.7908/C15B01H6
- Overview
+ Introduction
- Summary
  • MAF used for this analysis:KICH-TP.final_analysis_set.maf

  • Blacklist used for this analysis: pancan_mutation_blacklist.v14.hg19.txt

  • Significantly mutated genes (q ≤ 0.1): 30

  • Mutations seen in COSMIC: 43

  • Significantly mutated genes in COSMIC territory: 2

  • Significantly mutated genesets: 31

  • Significantly mutated genesets: (excluding sig. mutated genes):0

Mutation Preprocessing
  • Read 66 MAFs of type "Baylor-Illumina"

  • Total number of mutations in input MAFs: 7559

  • After removing 34 mutations outside chr1-24: 7525

  • After removing 520 blacklisted mutations: 7005

  • After removing 225 noncoding mutations: 6780

  • After collapsing adjacent/redundant mutations: 6767

Mutation Filtering
  • Number of mutations before filtering: 6767

  • After removing 282 mutations outside gene set: 6485

  • After removing 92 mutations outside category set: 6393

  • After removing 1 "impossible" mutations in

  • gene-patient-category bins of zero coverage: 6018

- Results
+ Breakdown of Mutations by Type
+ Breakdown of Mutation Rates by Category Type
+ Target Coverage for Each Individual
+ Distribution of Mutation Counts, Coverage, and Mutation Rates Across Samples
+ Lego Plots
+ CoMut Plot
+ Significantly Mutated Genes
+ COSMIC analyses
+ Geneset Analyses
+ Methods & Data