This report serves to describe the mutational landscape and properties of a given individual set, as well as rank genes and genesets according to mutational significance. MutSig vS2N was used to generate the results found in this report.
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Working with individual set: KIRP-TP
The input for this pipeline is a set of individuals with the following files associated for each:
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An annotated .maf file describing the mutations called for the respective individual, and their properties.
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A .wig file that contains information about the coverage of the sample.
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MAF used for this analysis:KIRP-TP.final_analysis_set.maf
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Significantly mutated genes (q ≤ 0.1): 29
Column Descriptions:
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N = number of sequenced bases in this gene across the individual set
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nnon = number of (nonsilent) mutations in this gene across the individual set
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nnull = number of (nonsilent) null mutations in this gene across the individual set
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nflank = number of noncoding mutations from this gene's flanking region, across the individual set
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nsil = number of silent mutations in this gene across the individual set
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p = p-value (overall)
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q = q-value, False Discovery Rate (Benjamini-Hochberg procedure)
gene | N | nflank | nsil | nnon | nnull | p | q |
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NF2 | 20909 | 0 | 0 | 5 | 5 | 4.7e-93 | 8.9e-89 |
KDM6A | 47174 | 0 | 0 | 6 | 6 | 1.1e-78 | 1.1e-74 |
PCF11 | 48410 | 0 | 1 | 8 | 0 | 1e-51 | 6.4e-48 |
IL32 | 6077 | 0 | 0 | 4 | 4 | 2.9e-41 | 1.4e-37 |
STAG2 | 51191 | 0 | 1 | 5 | 5 | 1.9e-38 | 7e-35 |
MET | 54796 | 0 | 0 | 8 | 0 | 2e-29 | 6.4e-26 |
SETD2 | 76014 | 0 | 0 | 6 | 5 | 3.9e-26 | 1e-22 |
FGFR3 | 17407 | 0 | 2 | 5 | 0 | 2.1e-23 | 5e-20 |
FLJ46321 | 53766 | 0 | 1 | 7 | 3 | 2.5e-22 | 5.3e-19 |
SRCAP | 85799 | 0 | 1 | 7 | 2 | 2.9e-14 | 5.5e-11 |
SRRM2 | 74469 | 0 | 1 | 6 | 1 | 5e-11 | 8.2e-08 |
ATP1A1 | 38419 | 0 | 0 | 5 | 0 | 5.2e-11 | 8.2e-08 |
RERE | 40582 | 0 | 1 | 5 | 1 | 1.8e-10 | 2.7e-07 |
QRICH2 | 48307 | 0 | 0 | 5 | 1 | 6.7e-09 | 9e-06 |
SLC5A12 | 22454 | 0 | 1 | 4 | 0 | 7.5e-09 | 9.3e-06 |
CDC27 | 30797 | 0 | 0 | 4 | 4 | 7.9e-09 | 9.3e-06 |
LGI4 | 6592 | 0 | 0 | 4 | 0 | 2.2e-08 | 0.000025 |
MLL2 | 128853 | 0 | 3 | 12 | 7 | 2.5e-08 | 0.000026 |
LRBA | 120098 | 0 | 1 | 6 | 4 | 2.1e-06 | 0.002 |
CMYA5 | 139668 | 0 | 0 | 6 | 1 | 3.2e-06 | 0.003 |
MUC16 | 475757 | 0 | 0 | 10 | 1 | 7.7e-06 | 0.0068 |
SFRS2IP | 55105 | 0 | 1 | 5 | 4 | 7.9e-06 | 0.0068 |
SYNE1 | 337943 | 0 | 0 | 8 | 1 | 0.000022 | 0.018 |
MLL3 | 166551 | 0 | 0 | 6 | 3 | 0.000025 | 0.019 |
FAT1 | 167684 | 0 | 1 | 6 | 2 | 0.000026 | 0.02 |
EP400 | 87653 | 0 | 0 | 5 | 1 | 0.000031 | 0.023 |
BOD1L | 94554 | 0 | 0 | 5 | 0 | 0.000066 | 0.046 |
MACF1 | 315386 | 0 | 2 | 9 | 0 | 0.000068 | 0.046 |
POLQ | 98468 | 0 | 0 | 5 | 1 | 0.000097 | 0.063 |
PARD6B | 13390 | 0 | 0 | 4 | 2 | 0.00016 | 0.1 |
SVEP1 | 111137 | 0 | 0 | 5 | 2 | 0.00028 | 0.17 |
FLG | 112270 | 0 | 1 | 5 | 1 | 0.0003 | 0.18 |
HERC1 | 148320 | 0 | 0 | 5 | 1 | 0.0022 | 1 |
SON | 82194 | 0 | 0 | 5 | 1 | 0.0045 | 1 |
BAP1 | 23072 | 0 | 1 | 4 | 1 | 0.0062 | 1 |
In brief, we tabulate the number of mutations and the number of covered bases for each gene. The counts are broken down by mutation context category: four context categories that are discovered by MutSig, and one for indel and 'null' mutations, which include indels, nonsense mutations, splice-site mutations, and non-stop (read-through) mutations. For each gene, we calculate the probability of seeing the observed constellation of mutations, i.e. the product P1 x P2 x ... x Pm, or a more extreme one, given the background mutation rates calculated across the dataset. [1]
This is an experimental feature. The full results of the analysis summarized in this report can be downloaded from the TCGA Data Coordination Center.