[med-svn] [trinityrnaseq] 02/02: manpage; mark scripts +x

Michael Crusoe misterc-guest at moszumanska.debian.org
Thu Feb 12 18:11:56 UTC 2015


This is an automated email from the git hooks/post-receive script.

misterc-guest pushed a commit to branch master
in repository trinityrnaseq.

commit 0be291ddbe454eba219bdc0bf774adf84b7a6c6c
Author: Michael R. Crusoe <mcrusoe at msu.edu>
Date:   Thu Feb 12 12:00:43 2015 -0500

    manpage; mark scripts +x
---
 debian/Trinity.1              | 110 ++++++++++++++++++++++++++++++++++++++++++
 debian/rules                  |  10 +++-
 debian/trinityrnaseq.manpages |   1 +
 3 files changed, 120 insertions(+), 1 deletion(-)

diff --git a/debian/Trinity.1 b/debian/Trinity.1
new file mode 100644
index 0000000..2358fbc
--- /dev/null
+++ b/debian/Trinity.1
@@ -0,0 +1,110 @@
+.\" DO NOT MODIFY THIS FILE!  It was generated by help2man 1.44.1.
+.TH TRINITY "1" "February 2015" "Trinity version: Trinity_v2.0.2" "User Commands"
+.SH NAME
+Trinity \- RNA-Seq De novo Assembly
+.SH DESCRIPTION
+###############################################################################
+#
+#     ______  ____   ____  ____   ____  ______  __ __
+#    |      ||    \e |    ||    \e |    ||      ||  |  |
+#    |      ||  D  ) |  | |  _  | |  | |      ||  |  |
+#    |_|  |_||    /  |  | |  |  | |  | |_|  |_||  ~  |
+#      |  |  |    \e  |  | |  |  | |  |   |  |  |___, |
+#      |  |  |  .  \e |  | |  |  | |  |   |  |  |     |
+#      |__|  |__|\e_||____||__|__||____|  |__|  |____/
+#
+###############################################################################
+#
+# Required:
+#
+#  \fB\-\-seqType\fR <string>      :type of reads: ( fa, or fq )
+#
+#  \fB\-\-max_memory\fR <string>      :suggested max memory to use by Trinity where limiting can be enabled. (jellyfish, sorting, etc)
+#                            provied in Gb of RAM, ie.  '\-\-max_memory 10G'
+#
+#  If paired reads:
+#      \fB\-\-left\fR  <string>    :left reads, one or more (separated by space)
+#      \fB\-\-right\fR <string>    :right reads, one or more (separated by space)
+#
+#  Or, if unpaired reads:
+#      \fB\-\-single\fR <string>   :single reads, one or more (note, if single file contains pairs, can use flag: \fB\-\-run_as_paired\fR )
+#
+####################################
+##  Misc:  #########################
+#
+#  \fB\-\-SS_lib_type\fR <string>          :Strand\-specific RNA\-Seq read orientation.
+#                                   if paired: RF or FR,
+#                                   if single: F or R.   (dUTP method = RF)
+#                                   See web documentation.
+#
+#  \fB\-\-CPU\fR <int>                     :number of CPUs to use, default: 2
+#  \fB\-\-min_contig_length\fR <int>       :minimum assembled contig length to report
+#                                   (def=200)
+#
+#  \fB\-\-long_reads\fR <string>           :fasta file containing error\-corrected or circular consensus (CCS) pac bio reads
+#
+#  \fB\-\-genome_guided_bam\fR <string>    :genome guided mode, provide path to coordinate\-sorted bam file.
+#                                   (see genome\-guided param section under \fB\-\-show_full_usage_info\fR)
+#
+#  \fB\-\-jaccard_clip\fR                  :option, set if you have paired reads and
+#                                   you expect high gene density with UTR
+#                                   overlap (use FASTQ input file format
+#                                   for reads).
+#                                   (note: jaccard_clip is an expensive
+#                                   operation, so avoid using it unless
+#                                   necessary due to finding excessive fusion
+#                                   transcripts w/o it.)
+#
+#  \fB\-\-trimmomatic\fR                   :run Trimmomatic to quality trim reads
+#                                        see '\-\-quality_trimming_params' under full usage info for tailored settings.
+#
+#
+#  \fB\-\-normalize_reads\fR               :run in silico normalization of reads. Defaults to max. read coverage of 50.
+#                                       see '\-\-normalize_max_read_cov' under full usage info for tailored settings.
+#
+#  \fB\-\-no_distributed_trinity_exec\fR   :do not run Trinity phase 2 (assembly of partitioned reads), and stop after generating command list.
+#
+#
+#  \fB\-\-output\fR <string>               :name of directory for output (will be
+#                                   created if it doesn't already exist)
+#                                   default( your current working directory: "/home/mcrusoe/debian/trinityrnaseq/trinity_out_dir"
+#                                    note: must include 'trinity' in the name as a safety precaution! )
+#
+#  \fB\-\-full_cleanup\fR                  :only retain the Trinity fasta file, rename as ${output_dir}.Trinity.fasta
+#
+#  \fB\-\-cite\fR                          :show the Trinity literature citation
+#
+#  \fB\-\-version\fR                       :reports Trinity version (Trinity_v2.0.2) and exits.
+#
+#  \fB\-\-show_full_usage_info\fR          :show the many many more options available for running Trinity (expert usage).
+.PP
+###############################################################################
+#
+#  *Note, a typical Trinity command might be:
+#
+#        Trinity \fB\-\-seqType\fR fq \fB\-\-max_memory\fR 50G \fB\-\-left\fR reads_1.fq  \fB\-\-right\fR reads_2.fq \fB\-\-CPU\fR 6
+#
+#
+#    and for Genome\-guided Trinity:
+#
+#        Trinity \fB\-\-genome_guided_bam\fR rnaseq_alignments.csorted.bam \fB\-\-max_memory\fR 50G
+#                \fB\-\-genome_guided_max_intron\fR 10000 \fB\-\-CPU\fR 6
+#
+#     see: /usr/lib/trinityrnaseq/sample_data/test_Trinity_Assembly/
+#          for sample data and 'runMe.sh' for example Trinity execution
+#
+#     For more details, visit: http://trinityrnaseq.github.io
+#
+###############################################################################
+.SH "SEE ALSO"
+The full documentation for
+.B Trinity
+is maintained as a Texinfo manual.  If the
+.B info
+and
+.B Trinity
+programs are properly installed at your site, the command
+.IP
+.B info Trinity
+.PP
+should give you access to the complete manual.
diff --git a/debian/rules b/debian/rules
index 50d104d..adaa918 100755
--- a/debian/rules
+++ b/debian/rules
@@ -17,6 +17,9 @@ BUTTERFLY_LIBDIR := ${ROOT_DIR}/../Butterfly/src/lib
 export CLASSPATH=/usr/share/java/collections15.jar:/usr/share/java/gnu-getopt.jar:${BUTTERFLY_LIBDIR}/jung-algorithms-2.0.1.jar:${BUTTERFLY_LIBDIR}/jung-api-2.0.1.jar:${BUTTERFLY_LIBDIR}/jung-api-2.0.1.jar:${BUTTERFLY_LIBDIR}/jung-graph-impl-2.0.1.jar
 
 SOURCE_DIRECTORIES = Inchworm Chrysalis trinity-plugins/fastool trinity-plugins/parafly
+
+BASEDIR=debian/trinityrnaseq/usr/lib/trinityrnaseq
+
 %:
 	dh $@ --parallel
 
@@ -44,4 +47,9 @@ override_dh_install:
 	dh_install
 	find debian/trinityrnaseq -name '*.p?' | xargs sed -i \
 		's=^#!/usr/local/bin/perl=#!/usr/bin/perl='
-
+	chmod u+x \
+		${BASEDIR}/Analysis/DifferentialExpression/pairwise_summaries/class_to_separate_fpkm_matrices.pl \
+		${BASEDIR}/Analysis/FL_reconstruction_analysis/count_by_expression_quintile.pl \
+		${BASEDIR}/util/misc/capture_orig_n_unmapped_reads.pl \
+		${BASEDIR}/util/support_scripts/plugin_install_tests.sh \
+		${BASEDIR}/util/support_scripts/trinity_install_tests.sh
diff --git a/debian/trinityrnaseq.manpages b/debian/trinityrnaseq.manpages
new file mode 100644
index 0000000..eb2bcfa
--- /dev/null
+++ b/debian/trinityrnaseq.manpages
@@ -0,0 +1 @@
+debian/Trinity.1

-- 
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