table of contents
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 (2018-07-05 at 09:17:13)
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
- noshow-skipped Boolean
- Make show-skipped 'false'
- 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
- noskip-low-mr-genes Boolean
- Make skip-low-mr-genes 'false'
- 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
- nowu-annotation-headers Boolean
- Make wu-annotation-headers 'false'
- 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
- noseparate-truncations Boolean
- Make separate-truncations 'false'
- 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
- nomerge-concurrent-muts Boolean
- Make merge-concurrent-muts 'false'
- skip-non-coding Boolean
- Skip non-coding mutations from the provided MAF file
Default value 'true' if not specified
- noskip-non-coding Boolean
- Make skip-non-coding 'false'
- skip-silent Boolean
- Skip silent mutations from the provided MAF file
Default value 'true' if not specified
- noskip-silent Boolean
- Make skip-silent 'false'
- 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
- noshow-known-hits Boolean
- Make show-known-hits 'false'
- 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
- nouse-maf-in-glm Boolean
- Make use-maf-in-glm 'false'
- 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
- noverbose Boolean
- Make verbose 'false'
- 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)
2018-07-05 | perl v5.26.2 |