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CLI tool for bioinformatic in-depth exploration of small RNA-seq data

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sRNAPipe-cli

sRNAPipe version 1.2.1

Requirements:

  • Perl modules:
    • Statistics
    • Parallel::ForkManager
    • Statistics::R
    • Getopt::Long
    • String::Random
    • File::Copy::Recursive
    • Math::CDF
  • BWA aligner, version 0.7.12 or higher
  • BedTools, version 2.24.0 or higher
  • Samtools, version 1.5
  • R, version 3.1 or higher
  • R packages:
    • plotrix
    • bioconductor-sushi
    • RColorBrewer
    • ggplot2

Install:

Run:

perl Makefile.pl
make install

Usage:

srnapipe --fastq <fastq file 1> --fastq_n <name 1> [--fastq <fastq file 2> --fastq_n <name 2> --fastq <fastq file 3> -- fastq_n <name 3> ...] --ref <reference genome> [--build_index] --transcripts <transcripts> [--build_transcripts] --TE <transposable elements> [--build_TE] --miRNAs <miRNAs> [--build_miRNAs] --snRNAs <snRNAs> [--build_snRNAs] --rRNAs <rRNAs> [--build_rRNAs] --tRNAs <tRNAs> [--buid_tRNAs] --dir <results directory> --html <results.html> [options]

Arguments:

Argument Description
--fastq Fastq file to process
--fastq_n Name of the content to process
--ref Fasta file containing the reference genome
--transcripts Fasta file containing the transcripts
--TE Fasta file containing the transposable elements
--miRNAs Fasta file containing the miRNAs
--snRNAs Fasta file containing the snRNAs
--rRNAs Fasta file containing the rRNAs
--tRNAs Fasta file containing the tRNAs
--html Main HTML file where results will be displayed
--dir Folder where results will be stored

For any fasta file, if a bwa index is not provided, you should build it through the corresponding '--build_[element]' argument

Options:

Option Description
--min <INT> Minimum read size (default: 18)
--max <INT> Maximum read size (default: 29)
--si_min <INT> Lower bound of siRNA range (default: 21)
--si_max <INT> Higher bound of siRNA range (default: 21)
--pi_min <INT> Lower bound of piRNA range (default: 23)
--pi_max <INT> Higher bound of piRNA range (default: 29)
--mis <INT> Maximal genome mismatches (default: 0)
--misTE <INT> Maximal TE mismatches (default: 3)
--PPPon <true|false> Ping-pong partners (default: true)

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CLI tool for bioinformatic in-depth exploration of small RNA-seq data

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