Description Usage Arguments Details Examples
Multiple traditional methods to identify significantly mutated genes based on outputs (*.categs.txt, *.coverage.txt, *.mutations.txt) produced by MutSigCV.
1 |
categs.file |
File with categories mutation rate from MutSigCV, often ended with |
coverage.file |
Coverage file from MutSigCV, often ended with |
mutations.file |
Mutation file from MutSigCV, often ended with |
mut.df |
A data frame of |
sep |
|
output.file |
Output file. |
method |
Method used to identify SMG. |
exclude.noncoding |
If TRUR, exclude |
N |
Permutation times used in |
trace |
If TRUE, print tracing message. |
only.CGC |
If TRUE, only considers cancer gene census. |
GOI |
A vector of gene-of-interest(GOI), if provided, |
mutations.file.formatted_as_csv |
Formatted |
The poisson convolution test (PCT
) proposed by Kan et al. in Diverse somatic mutation patterns and pathway alterations in human cancers
.
The Fisher's combined P-value test (FCPT
) and likelihood ratio test (LRT
) were 2 of the 3 tests proposed in MuSiC.
The perm.score
is a permutation procedure used to compute p-value for statistic Sg
proposed in page 16 of supplementary of MutSigCV.
The perm.num
permutes mutation number, instead of Sg
, to compute p-value.
PCT
, FCPT
and perm.score
are recommended to use.
1 2 3 4 | categs.file = "TCGA.Breast_Cancer.MutSigCV.categs.txt"
coverage.file = "TCGA.Breast_Cancer.MutSigCV.coverage.txt"
mutations.file = "TCGA.Breast_Cancer.MutSigCV.mutations.txt"
mutsig.gene(categs.file, coverage.file, mutations.file, sep="\t", output.file="out.PCT")
|
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