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: LGG-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:LGG-TP.final_analysis_set.maf
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Significantly mutated genes (q ≤ 0.1): 159
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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KRAS | 3502 | 0 | 0 | 24 | 0 | 0 | 0 |
ZNF860 | 68 | 0 | 0 | 6 | 0 | 0 | 0 |
TP53 | 4284 | 0 | 0 | 22 | 12 | 0 | 0 |
VAMP3 | 1326 | 0 | 0 | 7 | 7 | 0 | 0 |
SPDYE5 | 3298 | 0 | 0 | 8 | 0 | 0 | 0 |
ZNF479 | 6834 | 0 | 0 | 9 | 0 | 0 | 0 |
ZNF57 | 6902 | 0 | 2 | 11 | 0 | 0 | 0 |
LNP1 | 2380 | 0 | 1 | 7 | 7 | 0 | 0 |
CRIPAK | 3502 | 0 | 0 | 8 | 8 | 0 | 0 |
OR10A7 | 4216 | 0 | 0 | 8 | 8 | 6.4e-305 | 1.2e-301 |
CD300A | 3264 | 0 | 0 | 7 | 7 | 1.1e-290 | 1.9e-287 |
HMGB2 | 2652 | 0 | 0 | 6 | 6 | 3.2e-236 | 5e-233 |
GIGYF1 | 9180 | 0 | 0 | 10 | 10 | 3.1e-217 | 4.5e-214 |
HOXB2 | 2924 | 0 | 0 | 6 | 6 | 2.1e-214 | 2.8e-211 |
DMRT3 | 4080 | 0 | 0 | 9 | 1 | 3.3e-214 | 4.1e-211 |
FUZ | 3366 | 0 | 0 | 6 | 6 | 1.9e-186 | 2.2e-183 |
TREML2 | 3434 | 0 | 0 | 6 | 6 | 8.8e-183 | 9.8e-180 |
PTTG1IP | 1836 | 0 | 0 | 5 | 5 | 5.9e-175 | 6.2e-172 |
TTBK2 | 14246 | 0 | 0 | 11 | 11 | 6.8e-166 | 6.7e-163 |
F5 | 28016 | 0 | 1 | 8 | 0 | 1.7e-159 | 1.6e-156 |
HFE2 | 3978 | 0 | 0 | 6 | 6 | 5.8e-158 | 5.2e-155 |
CDKN2A | 2040 | 0 | 0 | 6 | 5 | 1.1e-157 | 9.4e-155 |
LRP10 | 6222 | 0 | 1 | 7 | 7 | 4.6e-153 | 3.8e-150 |
CHRD | 7446 | 0 | 0 | 5 | 0 | 4e-118 | 3.1e-115 |
TCF20 | 20434 | 0 | 0 | 11 | 11 | 6.8e-116 | 5.1e-113 |
UTP3 | 5474 | 0 | 0 | 6 | 6 | 4.4e-115 | 3.2e-112 |
TSPAN4 | 2822 | 0 | 0 | 6 | 4 | 1.1e-111 | 7.5e-109 |
SMAD4 | 6188 | 0 | 0 | 8 | 4 | 1.1e-104 | 7.3e-102 |
LYPD3 | 3162 | 0 | 0 | 5 | 5 | 2.6e-102 | 1.7e-99 |
FTSJ3 | 10200 | 0 | 0 | 7 | 7 | 1e-93 | 6.6e-91 |
TMCC1 | 7446 | 0 | 0 | 8 | 6 | 3.8e-87 | 2.3e-84 |
ADAD1 | 7514 | 0 | 0 | 6 | 6 | 4.4e-84 | 2.6e-81 |
OR10A2 | 3944 | 0 | 0 | 5 | 5 | 3e-82 | 1.7e-79 |
MAGEA10 | 4250 | 0 | 0 | 5 | 5 | 2.1e-76 | 1.1e-73 |
AADACL3 | 4318 | 0 | 0 | 5 | 5 | 3.2e-75 | 1.7e-72 |
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.