# HG changeset patch
# User peterjc
# Date 1415103350 18000
# Node ID c961d16801e488170667363c7d5f850f4fc9092a
Uploaded v0.0.2
diff -r 000000000000 -r c961d16801e4 test-data/sam_spec_padded.bam
Binary file test-data/sam_spec_padded.bam has changed
diff -r 000000000000 -r c961d16801e4 test-data/sam_spec_padded.bam2fq.fastq
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/sam_spec_padded.bam2fq.fastq Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,12 @@
+>ref
+AGCATGTTAGATAAGATAGCTGTGCTAGTAGGCAGTCAGCGCCAT
+>r001/1
+TTAGATAAAGGATACTG
+>r002
+AAAAGATAAGGATA
+>r003
+AGCTAA
+>r004
+ATAGCTTCAGC
+>r001/2
+ATGCCGCTG
diff -r 000000000000 -r c961d16801e4 test-data/sam_spec_padded.bam2fq_no_suf.fastq
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/sam_spec_padded.bam2fq_no_suf.fastq Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,12 @@
+>ref
+AGCATGTTAGATAAGATAGCTGTGCTAGTAGGCAGTCAGCGCCAT
+>r001
+TTAGATAAAGGATACTG
+>r002
+AAAAGATAAGGATA
+>r003
+AGCTAA
+>r004
+ATAGCTTCAGC
+>r001
+ATGCCGCTG
diff -r 000000000000 -r c961d16801e4 test-data/sam_spec_padded.bam2fq_pairs.fastq
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/sam_spec_padded.bam2fq_pairs.fastq Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,4 @@
+>r001/1
+TTAGATAAAGGATACTG
+>r001/2
+ATGCCGCTG
diff -r 000000000000 -r c961d16801e4 test-data/sam_spec_padded.bam2fq_singles.fastq
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/sam_spec_padded.bam2fq_singles.fastq Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,8 @@
+>r002
+AAAAGATAAGGATA
+>r003
+AGCTAA
+>r004
+ATAGCTTCAGC
+>ref
+AGCATGTTAGATAAGATAGCTGTGCTAGTAGGCAGTCAGCGCCAT
diff -r 000000000000 -r c961d16801e4 test-data/sam_spec_padded.depad.bam
Binary file test-data/sam_spec_padded.depad.bam has changed
diff -r 000000000000 -r c961d16801e4 test-data/sam_spec_padded.sam
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/sam_spec_padded.sam Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,10 @@
+@HD VN:1.5 SO:coordinate
+@SQ SN:ref LN:47
+ref 516 ref 1 0 14M2D31M * 0 0 AGCATGTTAGATAAGATAGCTGTGCTAGTAGGCAGTCAGCGCCAT *
+r001 99 ref 7 30 14M1D3M = 39 41 TTAGATAAAGGATACTG *
+* 768 ref 8 30 1M * 0 0 * * CT:Z:.;Warning;Note=Ref wrong?
+r002 0 ref 9 30 3S6M1D5M * 0 0 AAAAGATAAGGATA * PT:Z:1;4;+;homopolymer
+r003 0 ref 9 30 5H6M * 0 0 AGCTAA * NM:i:1
+r004 0 ref 18 30 6M14D5M * 0 0 ATAGCTTCAGC *
+r003 2064 ref 31 30 6H5M * 0 0 TAGGC * NM:i:0
+r001 147 ref 39 30 9M = 7 -41 CAGCGGCAT * NM:i:1
diff -r 000000000000 -r c961d16801e4 tools/samtools_bam2fq/README.rst
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tools/samtools_bam2fq/README.rst Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,104 @@
+Galaxy wrapper for samtools bam2fq
+====================================
+
+This wrapper is copyright 2014 by Peter Cock, The James Hutton Institute
+(formerly SCRI, Scottish Crop Research Institute), UK. All rights reserved.
+See the licence text below.
+
+This is a wrapper for part of the command line samtools suite.
+
+This wrapper is available from the Galaxy Tool Shed at:
+http://toolshed.g2.bx.psu.edu/view/peterjc/samtools_bam2fq
+
+
+Automated Installation
+======================
+
+This should be straightforward, Galaxy should automatically download and install
+samtools if required.
+
+
+Manual Installation
+===================
+
+This expects samtools to be on the $PATH, and was tested using v0.1.19.
+
+To install the wrapper copy or move the following files under the Galaxy tools
+folder, e.g. in a ``tools/samtools_bam2fq`` folder:
+
+* ``samtools_bam2fq.xml`` (the Galaxy tool definition)
+* ``README.rst`` (this file)
+
+You will also need to modify the ``tools_conf.xml`` file to tell Galaxy to offer
+the tool. Just add the line, perhaps under the NGS tools section::
+
+
+
+If you wish to run the unit tests, also move/copy the ``test-data/`` files
+under Galaxy's ``test-data/`` folder. Then::
+
+ $ ./run_tests.sh -id samtools_bam2fq
+
+That's it.
+
+
+History
+=======
+
+======= ======================================================================
+Version Changes
+------- ----------------------------------------------------------------------
+v0.0.1 - Initial public release, tested with samtools v1.1.
+v0.0.2 - Defaults to pair-aware mode which requires pre-sorting by read name.
+======= ======================================================================
+
+
+Developers
+==========
+
+Development is on this GitHub repository:
+https://github.com/peterjc/pico_galaxy/tree/master/tools/samtools_bam2fq
+
+For making the "Galaxy Tool Shed" http://toolshed.g2.bx.psu.edu/ tarball use
+the following command from the Galaxy root folder::
+
+ $ tar -czf samtools_bam2fq.tar.gz tools/samtools_bam2fq/README.rst tools/samtools_bam2fq/samtools_bam2fq.xml tools/samtools_bam2fq/tool_dependencies.xml test-data/sam_spec_padded.bam test-data/sam_spec_padded.sam test-data/sam_spec_padded.depad.bam test-data/sam_spec_padded.bam2fq.fastq test-data/sam_spec_padded.bam2fq_no_suf.fastq test-data/sam_spec_padded.bam2fq_singles.fastq test-data/sam_spec_padded.bam2fq_pairs.fastq
+
+Check this worked::
+
+ $ tar -tzf samtools_bam2fq.tar.gz
+ tools/samtools_bam2fq/README.rst
+ tools/samtools_bam2fq/samtools_bam2fq.xml
+ tools/samtools_bam2fq/tool_dependencies.xml
+ test-data/sam_spec_padded.bam
+ test-data/sam_spec_padded.sam
+ test-data/sam_spec_padded.depad.bam
+ test-data/sam_spec_padded.bam2fq.fastq
+ test-data/sam_spec_padded.bam2fq_no_suf.fastq
+ test-data/sam_spec_padded.bam2fq_singles.fastq
+ test-data/sam_spec_padded.bam2fq_pairs.fastq
+
+
+Licence (MIT)
+=============
+
+Permission is hereby granted, free of charge, to any person obtaining a copy
+of this software and associated documentation files (the "Software"), to deal
+in the Software without restriction, including without limitation the rights
+to use, copy, modify, merge, publish, distribute, sublicense, and/or sell
+copies of the Software, and to permit persons to whom the Software is
+furnished to do so, subject to the following conditions:
+
+The above copyright notice and this permission notice shall be included in
+all copies or substantial portions of the Software.
+
+THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR
+IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,
+FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE
+AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER
+LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM,
+OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN
+THE SOFTWARE.
+
+NOTE: This is the licence for the Galaxy Wrapper only.
+samtools is available and licenced separately.
diff -r 000000000000 -r c961d16801e4 tools/samtools_bam2fq/samtools_bam2fq.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tools/samtools_bam2fq/samtools_bam2fq.xml Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,137 @@
+
+ samtools bam2fq
+
+ samtools
+ samtools
+
+ samtools 2>&1 | grep -i "Version:"
+
+ #if $action_mode.mode == "pairs":
+ ## Sort by name for pair-aware output (should give nice interlaced FASTQ)
+ ## Galaxy has a tendancy to automatically apply co-ordindate sorting,
+ ## so just do this every time. If it was name sorted, pay an IO overhead.
+ ## Note requiring -T is samtools issue 295
+ samtools sort -n -O bam -T TEMP_SORT "$input_bam" | samtools bam2fq -s "$singletons_fastq" - > "$pairs_fastq"
+ #else
+ ## Naive conversion using order in the input file
+ samtools bam2fq $suffices $orig_qual "$input_bam" > "$out_fastq"
+ #end if
+
+
+
+
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+ (action_mode['mode'] == 'pairs')
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+
+ (action_mode['mode'] == 'pairs')
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+
+ (action_mode['mode'] == 'naive')
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+
+
+**What it does**
+
+This tool runs the ``samtools bam2fq`` command in the SAMtools toolkit.
+
+By default this will pre-sort your SAM/BAM file by read name and split your
+reads into an interlaced FASTQ file for paired reads, and a separate FASTQ
+file for singleton reads. A naive conversion is also offered which gives a
+single FASTQ file with the reads ordered as in the input SAM/BAM file.
+
+It is quite common to wish to remap high-throughput sequencing data. If you
+only have the mapped reads in SAM/BAM format, this tool can "unmap" them to
+recover FASTQ format reads to input into an alternative mapping tool.
+
+BAM files can hold both aligned reads and unaligned reads, so another example
+usage would be to filter your BAM file to get only the unaligned reads, and
+turn those back in FASTQ using this tool ready for *de novo* assembly, or to
+try mapping against another reference sequence.
+
+
+**Citation**
+
+If you use this Galaxy tool in work leading to a scientific publication please
+cite:
+
+Heng Li et al (2009). The Sequence Alignment/Map format and SAMtools.
+Bioinformatics 25(16), 2078-9.
+http://dx.doi.org/10.1093/bioinformatics/btp352
+
+Peter J.A. Cock (2014), Galaxy wrapper for the samtools bam2fq command
+http://toolshed.g2.bx.psu.edu/view/peterjc/samtools_bam2fq
+
+This wrapper is available to install into other Galaxy Instances via the Galaxy
+Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/samtools_bam2fq
+
+
+ 10.1093/bioinformatics/btp352
+
+
diff -r 000000000000 -r c961d16801e4 tools/samtools_bam2fq/tool_dependencies.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tools/samtools_bam2fq/tool_dependencies.xml Tue Nov 04 07:15:50 2014 -0500
@@ -0,0 +1,6 @@
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