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GMT-MUSIC-GALAXY(1p) User Contributed Perl Documentation GMT-MUSIC-GALAXY(1p)
 

gmt music galaxy

NAME

gmt music galaxy - Run the full suite of MuSiC tools sequentially.

VERSION

This document describes gmt music galaxy version 0.04 (2013-05-14 at 16:03:05)

SYNOPSIS

gmt music galaxy [--output-dir=?] --bam-list=? --output-bundle=? --roi-file=? --reference-sequence=? --maf-file=? --pathway-file=? [--numeric-clinical-data-file=?] [--categorical-clinical-data-file=?] [--mutation-matrix-file=?] [--permutations=?] [--normal-min-depth=?] [--tumor-min-depth=?] [--min-mapq=?] [--show-skipped] [--genes-to-ignore=?] [--bmr=?] [--max-proximity=?] [--bmr-modifier-file=?] [--numerical-data-test-method=?] [--skip-low-mr-genes] [--max-fdr=?] [--genetic-data-type=?] [--wu-annotation-headers] [--bmr-groups=?] [--separate-truncations] [--merge-concurrent-muts] [--skip-non-coding] [--skip-silent] [--min-mut-genes-per-path=?] [--glm-model-file=?] [--processors=?] [--aa-range=?] [--nuc-range=?] [--reference-build=?] [--show-known-hits] [--glm-clinical-data-file=?] [--use-maf-in-glm] [--omimaa-dir=?] [--cosmic-dir=?] [--verbose] [--clinical-correlation-matrix-file=?]
This tool takes as parameters all the information required to run the individual tools. An example usage is: 
 ... music play \
        --bam-list input/bams_to_analyze.txt \
        --numeric-clinical-data-file input/numeric_clinical_data.csv \
        --maf-file input/myMAF.tsv \
        --output-dir play_output_dir \
        --pathway-file input/pathway_db \
        --reference-sequence input/refseq/all_sequences.fa \
        --roi-file input/all_coding_regions.bed \
        --genetic-data-type gene

REQUIRED ARGUMENTS

bam-list Text
Tab delimited list of BAM files [sample_name normal_bam tumor_bam]
output-bundle Text
Location where Galaxy would like the bundle of Music outputs to be saved
roi-file Text
Tab delimited list of ROIs [chr start stop gene_name]
reference-sequence Text
Path to reference sequence in FASTA format
maf-file Text
List of mutations using TCGA MAF specifications v2.3
pathway-file Text
Tab-delimited file of pathway information

OPTIONAL ARGUMENTS

output-dir
Directory where output files and subdirectories will be written
Default value '' if not specified
numeric-clinical-data-file Text
Table of samples (y) vs. numeric clinical data category (x)
categorical-clinical-data-file Text
Table of samples (y) vs. categorical clinical data category (x)
mutation-matrix-file Text
Optionally store the sample-vs-gene matrix used during calculations.
permutations Number
Number of permutations used to determine P-values
normal-min-depth Integer
The minimum read depth to consider a Normal BAM base as covered
tumor-min-depth Integer
The minimum read depth to consider a Tumor BAM base as covered
min-mapq Integer
The minimum mapping quality of reads to consider towards read depth counts
show-skipped Boolean
Report each skipped mutation, not just how many
Default value 'false' (--noshow-skipped) if not specified
genes-to-ignore Text
Comma-delimited list of genes to ignore for background mutation rates
bmr Number
Background mutation rate in the targeted regions
max-proximity Text
Maximum AA distance between 2 mutations
bmr-modifier-file Text
Tab delimited list of values per gene that modify BMR before testing [gene_name bmr_modifier]
numerical-data-test-method Text
Either 'cor' for Pearson Correlation or 'wilcox' for the Wilcoxon Rank-Sum Test for numerical clinical data.
Default value 'cor' if not specified
skip-low-mr-genes Boolean
Skip testing genes with MRs lower than the background MR
Default value 'true' if not specified
max-fdr Number
The maximum allowed false discovery rate for a gene to be considered an SMG
Default value '0.2' if not specified
genetic-data-type Text
Data in matrix file must be either "gene" or "variant" type data
wu-annotation-headers Boolean
Use this to default to wustl annotation format headers
bmr-groups Integer
Number of clusters of samples with comparable BMRs
Default value '1' if not specified
separate-truncations Boolean
Group truncational mutations as a separate category
Default value 'false' (--noseparate-truncations) if not specified
merge-concurrent-muts Boolean
Multiple mutations of a gene in the same sample are treated as 1
Default value 'false' (--nomerge-concurrent-muts) if not specified
skip-non-coding Boolean
Skip non-coding mutations from the provided MAF file
Default value 'true' if not specified
skip-silent Boolean
Skip silent mutations from the provided MAF file
Default value 'true' if not specified
min-mut-genes-per-path Integer
Pathways with fewer mutated genes than this will be ignored
Default value '1' if not specified
glm-model-file Text
File outlining the type of model, response variable, covariants, etc. for the GLM analysis. (See DESCRIPTION).
processors Integer
Number of processors to use in SMG (requires 'foreach' and 'doMC' R packages)
Default value '1' if not specified
aa-range Integer
Set how close a 'near' match is when searching for amino acid near hits
Default value '2' if not specified
nuc-range Integer
Set how close a 'near' match is when searching for nucleotide position near hits
Default value '5' if not specified
reference-build Text
Put either "Build36" or "Build37"
Default value 'Build37' if not specified
show-known-hits Boolean
When a finding is novel, show known AA in that gene
Default value 'true' if not specified
glm-clinical-data-file Text
Clinical traits, mutational profiles, other mixed clinical data (See DESCRIPTION).
use-maf-in-glm Boolean
Set this flag to use the variant matrix created from the MAF file as variant input to GLM analysis.
Default value 'false' (--nouse-maf-in-glm) if not specified
omimaa-dir Path
omim amino acid mutation database folder
cosmic-dir Path
cosmic amino acid mutation database folder
verbose Boolean
turn on to display larger working output
Default value 'true' if not specified
clinical-correlation-matrix-file Text
Optionally store the sample-vs-gene matrix used internally during calculations.

DESCRIPTION

This command can be used to run all of the MuSiC analysis tools on a set of data. Please see the individual tools for further description of the parameters.

AUTHORS

 Thomas B. Mooney, M.S.

CREDITS

Please see the credits for genome-music(1).

SEE ALSO

genome-music(1), genome-music-path-scan(1), genome-music-smg(1), genome-music-clinical-correlation(1), genome-music-mutation-relation(1), genome-music-cosmic-omim(1), genome-music-proximity(1), genome-music-pfam(1)
2013-05-14 perl v5.14.2