|GMT-MUSIC-BMR-CALC-BMR(1p)||User Contributed Perl Documentation||GMT-MUSIC-BMR-CALC-BMR(1p)|
gmt music bmr calc-bmr¶
gmt music bmr calc-bmr - Calculates mutation rates given per-gene coverage (from "music bmr calc-covg"), and a mutation list
This document describes gmt music bmr calc-bmr version 0.04 (2018-07-05 at 09:17:13)
gmt music bmr calc-bmr --bmr-output=? --roi-file=? --gene-mr-file=? --reference-sequence=? --bam-list=? --output-dir=? --maf-file=? [--skip-non-coding] [--skip-silent] [--bmr-groups=?] [--show-skipped] [--separate-truncations] [--merge-concurrent-muts] [--genes-to-ignore=?]
... music bmr calc-bmr \ --bam-list input_dir/bam_list \ --maf-file input_dir/myMAF.tsv \ --output-dir output_dir/ \ --reference-sequence input_dir/all_sequences.fa \ --roi-file input_dir/all_coding_exons.tsv ... music bmr calc-bmr \ --bam-list input_dir/bam_list \ --maf-file input_dir/myMAF.tsv \ --output-dir output_dir/ \ --reference-sequence input_dir/all_sequences.fa \ --roi-file input_dir/all_coding_exons.tsv \ --genes-to-ignore GENE1,GENE2
- bmr-output Number
- roi-file Text
- Tab delimited list of ROIs [chr start stop gene_name] (See DESCRIPTION)
- gene-mr-file Text
- reference-sequence Text
- Path to reference sequence in FASTA format
- bam-list Text
- Tab delimited list of BAM files [sample_name normal_bam tumor_bam] (See DESCRIPTION)
- output-dir Text
- Directory where output files will be written (Use the same one used with calc-covg)
- maf-file Text
- List of mutations using TCGA MAF specification v2.3
- 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'
- bmr-groups Integer
- Number of clusters of samples with comparable BMRs (See DESCRIPTION)
Default value '1' if not specified
- 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'
- 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'
- genes-to-ignore Text
- Comma-delimited list of genes to ignore for background mutation rates
Given a mutation list (MAF), and per-gene coverage data calculated using "music bmr calc-covg"), this script calculates overall Background Mutation Rate (BMR) and BMRs in the categories of AT/CG/CpG Transitions, AT/CG/CpG Transversions, and Indels. An optional category for truncational mutations can also be specified. The script generates a file with per-gene mutation rates that can be used with the tool that tests for significantly mutated genes (music smg).
- The regions of interest (ROIs) of each gene are typically regions targeted for sequencing or are merged exon loci (from multiple transcripts) of genes with 2-bp flanks (splice junctions). ROIs from the same chromosome must be listed adjacent to each other in this file. This allows the underlying C-based code to run much more efficiently and avoid re-counting bases seen in overlapping ROIs (for overall covered base counts). For per-gene base counts, an overlapping base will be counted each time it appears in an ROI of the same gene. To avoid this, be sure to merge together overlapping ROIs of the same gene. BEDtools' mergeBed can help if used per gene.
- Provide a file containing sample names and normal/tumor BAM locations for each. Use the tab- delimited format [sample_name normal_bam tumor_bam] per line. Additional columns like clinical data are allowed, but ignored. The sample_name must be the same as the tumor sample names used in the MAF file (16th column, with the header Tumor_Sample_Barcode).
- Ideally, we want to test the mutation rate (MR) of a gene in a sample against the background mutation rate (BMR) across that sample. But if the BMRs of some samples are comparable, we can instead test the MR of a gene across a group of samples with comparable BMR, against the overall BMR of that group. This argument specifies how many such groups you want to cluster samples into. By default, it is assumed that all samples have comparable BMRs (bmr-groups = 1).
Copyright (C) 2010-2011 Washington University in St. Louis.
It is released under the Lesser GNU Public License (LGPL) version 3. See the associated LICENSE file in this distribution.
Cyriac Kandoth, Ph.D.