App-SimulateReads
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lib/App/SimulateReads/Command/Genome.pm view on Meta::CPAN
package App::SimulateReads::Command::Genome;
# ABSTRACT: simulate command class. Simulate genome sequencing
use App::SimulateReads::Base 'class';
extends 'App::SimulateReads::CLI::Command';
with 'App::SimulateReads::Role::Digest';
our $VERSION = '0.16'; # VERSION
sub default_opt {
'paired-end-id' => '%i.%U_%c_%s_%S_%E',
'single-end-id' => '%i.%U_%c_%s_%t_%n',
'seed' => time,
'verbose' => 0,
'prefix' => 'out',
'output-dir' => '.',
'jobs' => 1,
'gzip' => 1,
'count-loops-by' => 'coverage',
'coverage' => 8,
'strand-bias' => 'random',
'seqid-weight' => 'length',
'sequencing-type' => 'paired-end',
'fragment-mean' => 300,
'fragment-stdd' => 50,
'sequencing-error' => 0.005,
'read-size' => 100,
'quality-profile' => 'poisson'
}
sub rm_opt {
'strand-bias',
'number-of-reads',
'seqid-weight',
'expression-matrix'
}
__END__
=pod
=encoding UTF-8
=head1 NAME
App::SimulateReads::Command::Genome - simulate command class. Simulate genome sequencing
=head1 VERSION
version 0.16
=head1 SYNOPSIS
simulate_reads genome [options] <fasta-file>
Arguments:
a fasta-file
Options:
-h, --help brief help message
-M, --man full documentation
-v, --verbose print log messages
-p, --prefix prefix output [default:"out"]
-o, --output-dir output directory [default:"."]
-i, --append-id append to the defined template id [Format]
-I, --id overlap the default template id [Format]
-j, --jobs number of jobs [default:"1"; Integer]
-z, --gzip compress output file
-s, --seed set the seed of the base generator
[default:"time()"; Integer]
-c, --coverage fastq-file coverage [default:"8", Number]
-t, --sequencing-type single-end or paired-end reads
[default:"paired-end"]
-q, --quality-profile illumina sequencing system profiles
[default:"poisson"]
-e, --sequencing-error sequencing error rate
[default:"0.005"; Number]
-r, --read-size the read size [default:"100"; Integer]
the quality_profile from database overrides
this value
-m, --fragment-mean the fragment mean size for paired-end reads
[default:"300"; Integer]
-d, --fragment-stdd the fragment standard deviation size for
paired-end reads [default:"50"; Integer]
=head1 DESCRIPTION
Simulate genome sequencing.
=head1 OPTIONS
=over 8
=item B<--help>
Print a brief help message and exits.
=item B<--man>
Prints the manual page and exits.
=item B<--verbose>
Prints log information to standard error
=item B<--prefix>
Concatenates the prefix to the output-file name.
=item B<--output-dir>
Creates output-file inside output-dir. If output-dir
does not exist, it is created recursively
=item B<--append-id>
Append string template to the defined template id.
See B<Format>
=item B<--id>
Overlap the default defined template id:
I<single-end> %i.%U_%c_%s_%t_%n and I<paired-end> %i.%U_%c_%s_%S_%E
e.g. SR123.1_chr1_P_1001_1101
See B<Format>
=item B<Format>
A string B<Format> is a combination of literal and escape characters similar to the way I<printf> works.
That way, the user has the freedom to customize the fastq sequence identifier to fit her needs. Valid
escape characteres are:
Common escape characters
Escape Meaning
------ ------------------------------------------
%i instrument id composed by SR + PID
%I job slot number
%q quality profile
%e sequencing error
%R read 1, or 2 if it is the paired-end mate
%U read number
%r read size
%c sequence id as chromossome, ref
%s read or fragment strand
%t read start position
%n read end position
Paired-end specific escape characters
Escape Meaning
------ ------------------------------------------
%T mate read start position
%N mate read end position
%D distance between the paired-reads
%m fragment mean
%d fragment standard deviation
%f fragment size
%S fragment start position
%E fragment end position
=item B<--jobs>
Sets the number of child jobs to be created
=item B<--gzip>
Compress the output-file with gzip algorithm. It is
possible to pass --no-gzip if one wants
uncompressed output-file
=item B<--seed>
Sets the seed of the base generator. The ability to set the seed is
useful for those who want reproducible simulations. Pay attention to
the number of jobs (--jobs) set, because each job receives a different
seed calculated from the I<main seed>. So, for reproducibility, the
same seed set before needs the same number of jobs set before as well.
=item B<--read-size>
Sets the read size, if quality-profile is equal to 'poisson'. The
quality-profile from database overrides the read-size
=item B<--coverage>
Calculates the number of reads based on the sequence
coverage: number_of_reads = (sequence_size * coverage) / read_size.
This is the default option for genome sequencing simulation
=item B<--sequencing-type>
Sets the sequencing type to single-end or paired-end
=item B<--fragment-mean>
If the sequencing-type is set to paired-end, it sets the
fragment mean
=item B<--fragment-stdd>
If the sequencing-type is set to paired-end, it sets the
fragment standard deviation
=item B<--sequencing-error>
Sets the sequencing error rate. Valid values are between zero and one
=item B<--quality-profile>
Sets the illumina sequencing system profile for quality. For now, the unique
valid values are hiseq and poisson
=back
=head1 AUTHOR
Thiago L. A. Miller <tmiller@mochsl.org.br>
=head1 COPYRIGHT AND LICENSE
This software is Copyright (c) 2018 by Teaching and Research Institute from SÃrio-Libanês Hospital.
This is free software, licensed under:
The GNU General Public License, Version 3, June 2007
=cut
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