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package App::Sandy; |
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# ABSTRACT: App builder that simulates single-end and paired-end reads. |
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use App::Sandy::Base 'class'; |
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extends 'App::Sandy::CLI::App'; |
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our $VERSION = '0.22'; # VERSION |
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sub command_map { |
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genome => 'App::Sandy::Command::Genome', |
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transcriptome => 'App::Sandy::Command::Transcriptome', |
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quality => 'App::Sandy::Command::Quality', |
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expression => 'App::Sandy::Command::Expression', |
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variation => 'App::Sandy::Command::Variation', |
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version => 'App::Sandy::Command::Version', |
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citation => 'App::Sandy::Command::Citation' |
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} |
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__END__ |
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=pod |
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=encoding UTF-8 |
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=head1 NAME |
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App::Sandy - App builder that simulates single-end and paired-end reads. |
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=head1 VERSION |
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version 0.22 |
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=head1 SYNOPSIS |
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sandy [options] |
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sandy help <command> |
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sandy <command> ... |
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Options: |
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-h, --help brief help message |
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-u, --man full documentation |
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Help commands: |
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help show application or command-specific help |
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man show application or command-specific documentation |
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Misc commands: |
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version print the current version |
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citation export citation in BibTeX format |
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Database commands: |
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quality manage quality profile database |
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expression manage expression-matrix database |
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variation manage structural variation database |
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Main commands: |
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genome simulate genome sequencing |
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transcriptome simulate transcriptome sequencing |
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=head1 DESCRIPTION |
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B<Sandy> is a bioinformatic tool that provides a simple engine to generate |
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single-end/paired-end reads from a given fasta file. Many next-generation |
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sequencing analyses rely on hypothetical models and principles that are |
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not precisely satisfied in practice. Simulated data, which provides positive |
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controls, would be a perfect way to overcome these difficulties. Here, we |
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present Sandy, a straightforward, easy to use, fast, complete set of tools |
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to generate synthetic second and third-generation sequencing reads. Sandy |
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simulates whole genome sequencing, whole exome sequencing, RNAseq reads. |
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Sandy presents also several features to the users manipulate the data, as |
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well as well-organized database containing the âtrueâ information (based on |
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the generated data) of the reads position into the genome, gene and transcript |
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expression, sequencing errors, and the sequencing coverage. One of the most |
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impressive features of Sandy is the power to simulate polymorphisms as snvs, |
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indels and structural variations (e.g. gene duplication, retro-duplication, |
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gene-fusion) along with the sequencing reads - with no need of further processing |
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steps. Sandy can be used therefore for benchmarking results of a variety of |
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pipelines in the genomics or transcriptomics, as well as in generating new |
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hypotheses and helping in the best designing of sequencing projects, possibly |
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optimizing time and costs. |
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=head1 AUTHORS |
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=over 4 |
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=item * |
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Thiago L. A. Miller <tmiller@mochsl.org.br> |
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=item * |
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J. Leonel Buzzo <lbuzzo@mochsl.org.br> |
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=item * |
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Felipe R. C. dos Santos <fsantos@mochsl.org.br> |
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=item * |
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Helena B. Conceição <hconceicao@mochsl.org.br> |
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=item * |
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Gabriela Guardia <gguardia@mochsl.org.br> |
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=item * |
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Fernanda Orpinelli <forpinelli@mochsl.org.br> |
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=item * |
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Pedro A. F. Galante <pgalante@mochsl.org.br> |
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=back |
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=head1 COPYRIGHT AND LICENSE |
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This software is Copyright (c) 2018 by Teaching and Research Institute from SÃrio-Libanês Hospital. |
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This is free software, licensed under: |
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The GNU General Public License, Version 3, June 2007 |
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=cut |