Provided by: libgenome-model-tools-music-perl_0.04-1_all
genome music proximity
NAME
genome music proximity - Perform a proximity analysis on a list of mutations.
VERSION
This document describes genome music proximity version 0.04 (2013-05-25 at 17:45:01)
SYNOPSIS
genome music proximity --maf-file=? --output-dir=? [--max-proximity=?] [--skip-non-coding] [--skip-silent] ... music proximity \ --maf-file input_dir/myMAF.tsv \ --output-dir output_dir/ \ --max-proximity 15
REQUIRED ARGUMENTS
maf-file Text List of mutations using TCGA MAF specifications v2.3 output-dir Text Directory where output files will be written
OPTIONAL ARGUMENTS
max-proximity Text Maximum allowed AA distance between 2 mutations Default value '7' 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
DESCRIPTION
This module first calculates the amino acid position of each mutation in the MAF file within its respective transcript. Then, for each mutation, two values are calculated: 1) the number of other mutations on the same transcript within the proximity limit set by the max-proximity input parameter, and 2) the distance to the closest other mutation in this nearby set. Only mutations which have another mutation within close proximity are reported in the output-file. In addition to the standard version 2.3 MAF headers, there needs to be 3 columns appended. These column headers in the MAF must have these names in the header in order for the tool to find them: transcript_name - the transcript name, such as NM_000028 amino_acid_change - the amino acid change, such as p.R290H c_position - the nucleotide position changed, such as c.869 The output is generated with the folowing column headers: Mutations_Within_Proximity, Nearest_Mutation, Gene, Transcript, Affected_Amino_Acid(s), Chr, Start, Stop, Ref_Allele, Var_Allele, Sample
AUTHORS
Nathan D. Dees, Ph.D. Dan Koboldt, M.S. Cyriac Kandoth, Ph.D.