/usr/share/perl5/Genome/Model/Tools/Music.pm is in libgenome-model-tools-music-perl 0.04-3.
This file is owned by root:root, with mode 0o644.
The actual contents of the file can be viewed below.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 | package Genome::Model::Tools::Music;
use strict;
use warnings;
use Genome;
#bugfix version needs to be encoded as extra precision after the decimal point ie: .0401
our $VERSION = '0.04';
class Genome::Model::Tools::Music {
is => ['Command::Tree'],
doc => 'Mutational Significance in Cancer (Cancer Mutation Analysis)'
};
sub _doc_manual_body {
return <<EOS
The MuSiC suite is a set of tools aimed at discovering the significance of somatic mutations found within a given cohort of cancer samples, and with respect to a variety of external data sources. The standard inputs required are:
=over 4
=item 1. mapped reads in BAM format
=item 2. predicted or validated SNVs or indels in mutation annotation format (MAF)
=item 3. a list of regions of interest (typically the boundaries of coding exons)
=item 4. any relevant numeric or categorical clinical data.
=back
The formats for inputs 3. and 4. are:
=over 4
=item 3. Regions of Interest File:
=over 4
=item * Do not use headers
=item * 4 columns, which are [chromosome start-position(1-based) stop-position(1-based) gene_name]
=back
=item 4. Clinical Data Files:
=over 4
=item * Headers are required
=item * At least 1 sample_id column and 1 attribute column, with the format being [sample_id clinical_data_attribute clinical_data_attribute ...]
=item * The sample_id must match the sample_id listed in the MAF under "Tumor_Sample_Barcode" for relating the mutations of this sample.
=item * The header for each clinical_data_attribute will appear in the output file to denote relationships with the mutation data from the MAF.
=back
=back
Descriptions for the usage of each tool (each sub-command) can be found separately.
The B<play> command runs all of the sub-commands serially on a selected input set.
EOS
}
sub _doc_copyright_years {
(2007,2011);
}
sub _doc_license {
my $self = shift;
my (@y) = $self->_doc_copyright_years;
return <<EOS
Copyright (C) $y[0]-$y[1] 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.
EOS
}
sub _doc_authors {
return <<EOS
This software is developed by the analysis and engineering teams at
The Genome Institute at Washington University School of Medicine in St. Louis,
with funding from the National Human Genome Research Institute. Richard K. Wilson, P.I.
The primary authors of the MuSiC suite are:
Nathan D. Dees, Ph.D.
Cyriac Kandoth, Ph.D.
Dan Koboldt, M.S.
William Schierding, M.S.
Michael Wendl, Ph.D.
Qunyuan Zhang, Ph.D.
Thomas B. Mooney, M.S.
EOS
}
sub _doc_bugs {
return <<EOS;
For defects with any software in the genome namespace, contact
genome-dev ~at~ genome.wustl.edu.
EOS
}
sub _doc_credits {
return <<EOS,
The MuSiC suite uses tabix, by Heng Li. See http://samtools.sourceforge.net/tabix.shtml.
MuSiC depends on copies of data from the following databases, packaged in a form useable for quick analysis:
* KEGG - http://www.genome.jp/kegg/
* COSMIC - http://www.sanger.ac.uk/genetics/CGP/cosmic/
* OMIM - http://www.ncbi.nlm.nih.gov/omim
* Pfam - http://pfam.sanger.ac.uk/
* SMART - http://smart.embl-heidelberg.de/
* SUPERFAMILY - http://supfam.cs.bris.ac.uk/SUPERFAMILY/
* PatternScan - http://www.expasy.ch/prosite/
EOS
}
sub _doc_see_also {
'B<genome>(1)',
}
1;
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