# HG changeset patch
# User iuc
# Date 1479941757 18000
# Node ID e4b87a00b1dfd82c2489d8cc89a11645727acfa6
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/data_managers/data_manager_star_index_builder commit 3265247e909410db2a6d6087a2c0d3a9885c120c-dirty
diff -r 000000000000 -r e4b87a00b1df README
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/README Wed Nov 23 17:55:57 2016 -0500
@@ -0,0 +1,40 @@
+*What it does*
+
+This is a Galaxy datamanager for the rna STAR gap-aware RNA aligner. It's a hack of Dan Blankenberg's BWA data manager
+and works on any fasta file you have already downloaded with the all fasta data manager - start there!
+
+Warning - this is not well tested and there are some complexities to do with splice junction annotation in rna star
+indexes - feedback welcomed. Send code.
+
+Note, currently you'll need a small patch to prevent an error when you try to generate splice junction indexes described at
+https://bitbucket.org/galaxy/galaxy-central/pull-request/510/fix-for-data-manager-failure-to-update-a#comment-3265356
+
+Please read the fine manual - that and the google group are the places to learn about the options above.
+
+*Note on sjdbOverhang*
+
+From https://groups.google.com/forum/#!topic/rna-star/h9oh10UlvhI::
+
+ James is right, using large enough --sjdbOverhang is safer and should not generally cause any problems with reads of varying length. If your reads are very short, <50b, then I would strongly recommend using optimum --sjdbOverhang=mateLength-1
+ By mate length I mean the length of one of the ends of the read, i.e. it's 100 for 2x100b PE or 1x100b SE. For longer reads you can simply use generic --sjdbOverhang 100.
+ It is a bit confusing because of the way I named this parameter. --sjdbOverhang Noverhang is only used at the genome generation step for constructing the reference sequence out of the annotations.
+ Basically, the Noverhang exonic bases from the donor site and Noverhang exonic bases from the acceptor site are spliced together for each of the junctions, and these spliced sequences are added to the genome sequence.
+
+ At the mapping stage, the reads are aligned to both genomic and splice sequences simultaneously. If a read maps to one of spliced sequences and crosses the "junction" in the middle of it, the coordinates of two pspliced pieces are translated back to genomic space and added to the collection of mapped pieces, which are then all "stitched" together to form the final alignment. Since in the process of "maximal mapped length" search the read is split into pieces of no longer than --seedSearchStartLmax (=50 by default) bases, even if the read (mate) is longer than --sjdbOverhang, it can still be mapped to the spliced reference, as long as --sjdbOverhang > --seedSearchStartLmax.
+
+ Cheers
+ Alex
+
+*Note on gene model requirements for splice junctions*
+
+From https://groups.google.com/forum/#!msg/rna-star/3Y_aaTuzBrE/lUylTB8h5vMJ::
+
+ When you generate a genome with annotations, you need to specify --sjdbOverhang value, which ideally should be equal to (oneMateLength-1), or you could use a generic value of ~100.
+
+ Your gtf lines look fine to me. STAR needs 3 features from a GTF file:
+ 1. Chromosome names in col.1 that agree with chromosome names in genome .fasta files. If you have "chr2L" names in the genome .fasta files, and "2L" in the .gtf file, then you need to use --sjdbGTFchrPrefix chr option.
+ 2. 'exon' in col.3 for the exons of all transcripts (this name can be changed with --sjdbGTFfeatureExon)
+ 3. 'transcript_id' attribute that assigns each exon to a transcript (--this name can be changed with --sjdbGTFtagExonParentTranscript)
+
+ Cheers
+ Alex
diff -r 000000000000 -r e4b87a00b1df data_manager/rnastar_index_builder.py
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/data_manager/rnastar_index_builder.py Wed Nov 23 17:55:57 2016 -0500
@@ -0,0 +1,121 @@
+#!/usr/bin/env python
+# Dan Blankenberg
+# adapted from Dan's BWA one for rna star
+# ross lazarus sept 2014
+# fixed some stupid bugs January 2015
+import json
+import optparse
+import os
+import subprocess
+import sys
+import tempfile
+
+CHUNK_SIZE = 2**20
+ONE_GB = 2**30
+
+DEFAULT_DATA_TABLE_NAME = "rnastar_index"
+
+
+def get_id_name( params, dbkey, fasta_description=None):
+ # TODO: ensure sequence_id is unique and does not already appear in location file
+ sequence_id = params['param_dict']['sequence_id']
+ if not sequence_id:
+ sequence_id = dbkey
+
+ sequence_name = params['param_dict']['sequence_name']
+ if not sequence_name:
+ sequence_name = fasta_description
+ if not sequence_name:
+ sequence_name = dbkey
+ return sequence_id, sequence_name
+
+
+def _add_data_table_entry( data_manager_dict, data_table_name, data_table_entry ):
+ data_manager_dict['data_tables'] = data_manager_dict.get( 'data_tables', {} )
+ data_manager_dict['data_tables'][ data_table_name ] = data_manager_dict['data_tables'].get( data_table_name, [] )
+ data_manager_dict['data_tables'][ data_table_name ].append( data_table_entry )
+ return data_manager_dict
+
+
+def build_rnastar_index(data_manager_dict, fasta_filename, target_directory,
+ dbkey, sequence_id, sequence_name, data_table_name,
+ sjdbOverhang, sjdbGTFfile, sjdbFileChrStartEnd,
+ sjdbGTFtagExonParentTranscript, sjdbGTFfeatureExon,
+ sjdbGTFchrPrefix, n_threads):
+ # TODO: allow multiple FASTA input files
+ fasta_base_name = os.path.basename( fasta_filename )
+ sym_linked_fasta_filename = os.path.join( target_directory, fasta_base_name )
+ os.symlink( fasta_filename, sym_linked_fasta_filename )
+ # print >> sys.stdout,'made',sym_linked_fasta_filename
+ cl = ['STAR', '--runMode', 'genomeGenerate', '--genomeFastaFiles', sym_linked_fasta_filename, '--genomeDir', target_directory, '--runThreadN', n_threads ]
+
+ if sjdbGTFfile:
+ cl += [ '--sjdbGTFfeatureExon', sjdbGTFfeatureExon, '--sjdbGTFtagExonParentTranscript', sjdbGTFtagExonParentTranscript]
+ if (sjdbGTFchrPrefix > ''):
+ cl += ['--sjdbGTFchrPrefix', sjdbGTFchrPrefix]
+ cl += ['--sjdbOverhang', sjdbOverhang, '--sjdbGTFfile', sjdbGTFfile]
+ elif sjdbFileChrStartEnd:
+ cl += ['--sjdbFileChrStartEnd', sjdbFileChrStartEnd, '--sjdbOverhang', sjdbOverhang]
+
+ tmp_stderr = tempfile.NamedTemporaryFile( prefix="tmp-data-manager-rnastar-index-builder-stderr" )
+ proc = subprocess.Popen( args=cl, shell=False, cwd=target_directory, stderr=tmp_stderr.fileno() )
+ return_code = proc.wait()
+ if return_code:
+ tmp_stderr.flush()
+ tmp_stderr.seek(0)
+ print >> sys.stderr, "Error building index:"
+ while True:
+ chunk = tmp_stderr.read( CHUNK_SIZE )
+ if not chunk:
+ break
+ sys.stderr.write( chunk )
+ sys.exit( return_code )
+ tmp_stderr.close()
+ data_table_entry = dict( value=sequence_id, dbkey=dbkey, name=sequence_name, path=fasta_base_name )
+ data_manager_dict = _add_data_table_entry( data_manager_dict, data_table_name, data_table_entry )
+ return data_manager_dict
+
+
+def main():
+ # Parse Command Line
+ parser = optparse.OptionParser()
+ parser.add_option( '--fasta_filename', dest='fasta_filename', action='store', type="string", default=None, help='fasta_filename' )
+ parser.add_option( '--fasta_dbkey', dest='fasta_dbkey', action='store', type="string", default=None, help='fasta_dbkey' )
+ parser.add_option( '--fasta_description', dest='fasta_description', action='store', type="string", default=None, help='fasta_description' )
+ parser.add_option( '--data_table_name', dest='data_table_name', action='store', type="string", default=None, help='data_table_name' )
+ parser.add_option( '--sjdbGTFfile', type="string", default=None )
+ parser.add_option( '--sjdbGTFchrPrefix', type="string", default=None )
+ parser.add_option( '--sjdbGTFfeatureExon', type="string", default=None )
+ parser.add_option( '--sjdbGTFtagExonParentTranscript', type="string", default=None )
+ parser.add_option( '--sjdbFileChrStartEnd', type="string", default=None )
+ parser.add_option( '--sjdbOverhang', type="string", default='100' )
+ parser.add_option( '--runThreadN', type="string", default='4' )
+ (options, args) = parser.parse_args()
+ filename = args[0]
+ params = json.loads( open( filename ).read() )
+ target_directory = params[ 'output_data' ][0]['extra_files_path'].encode('ascii', 'replace')
+ dbkey = options.fasta_dbkey
+ if dbkey in [ None, '', '?' ]:
+ raise Exception( '"%s" is not a valid dbkey. You must specify a valid dbkey.' % ( dbkey ) )
+
+ sequence_id, sequence_name = get_id_name( params, dbkey=dbkey, fasta_description=options.fasta_description )
+
+ try:
+ os.mkdir( target_directory )
+ except OSError:
+ pass
+ # build the index
+ data_manager_dict = build_rnastar_index(
+ data_manager_dict={}, fasta_filename=options.fasta_filename,
+ target_directory=target_directory, dbkey=dbkey, sequence_id=sequence_id,
+ sequence_name=sequence_name, data_table_name=options.data_table_name,
+ sjdbOverhang=options.sjdbOverhang, sjdbGTFfile=options.sjdbGTFfile,
+ sjdbFileChrStartEnd=options.sjdbFileChrStartEnd,
+ sjdbGTFtagExonParentTranscript=options.sjdbGTFtagExonParentTranscript,
+ sjdbGTFfeatureExon=options.sjdbGTFfeatureExon,
+ sjdbGTFchrPrefix=options.sjdbGTFchrPrefix, n_threads=options.runThreadN)
+ open( filename, 'wb' ).write( json.dumps( data_manager_dict ) )
+
+
+if __name__ == "__main__":
+ main()
diff -r 000000000000 -r e4b87a00b1df data_manager/rnastar_index_builder.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/data_manager/rnastar_index_builder.xml Wed Nov 23 17:55:57 2016 -0500
@@ -0,0 +1,127 @@
+
+ builder
+
+ rnastar
+
+
+rnastar_index_builder.py "${out_file}" --fasta_filename "${all_fasta_source.fields.path}"
+--fasta_dbkey "${all_fasta_source.fields.dbkey}" --fasta_description "${all_fasta_source.fields.name}"
+--runThreadN 1
+#if $genemodel.modelformat=="gff3":
+#import pipes
+ --sjdbGTFchrPrefix ${ pipes.quote( str( $genemodel.sjdbGTFchrPrefix ) ) or "''" }
+ --sjdbOverhang "${genemodel.sjdbOverhang}"
+ --sjdbGTFfile "${genemodel.sjdbGTFfile}"
+ --sjdbGTFtagExonParentTranscript ${ pipes.quote( str( $genemodel.sjdbGTFtagExonParentTranscript ) ) or "''" }
+ --sjdbGTFfeatureExon ${ pipes.quote( str( $genemodel.sjdbGTFfeatureExon ) ) or "''" }
+#end if
+#if $genemodel.modelformat=="bed":
+ --sjdbFileChrStartEnd "${genemodel.sjdbFileChrStartEnd}"
+ --sjdbOverhang "${genemodel.sjdbOverhang}"
+#end if
+#if $genemodel.modelformat=="None":
+ --sjdbOverhang 0
+#end if
+--data_table_name "rnastar_index"
+
+
+
+
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+
+
+.. class:: infomark
+
+ --seedSearchStartLmax.
+
+ Cheers
+ Alex
+
+*Note on gene model requirements for splice junctions*
+
+From https://groups.google.com/forum/#!msg/rna-star/3Y_aaTuzBrE/lUylTB8h5vMJ::
+
+ When you generate a genome with annotations, you need to specify --sjdbOverhang value, which ideally should be equal to (oneMateLength-1), or you could use a generic value of ~100.
+
+ Your gtf lines look fine to me. STAR needs 3 features from a GTF file:
+ 1. Chromosome names in col.1 that agree with chromosome names in genome .fasta files. If you have "chr2L" names in the genome .fasta files, and "2L" in the .gtf file, then you need to use --sjdbGTFchrPrefix chr option.
+ 2. 'exon' in col.3 for the exons of all transcripts (this name can be changed with --sjdbGTFfeatureExon)
+ 3. 'transcript_id' attribute that assigns each exon to a transcript (--this name can be changed with --sjdbGTFtagExonParentTranscript)
+
+ Cheers
+ Alex
+
+**Notice:** If you leave name, description, or id blank, it will be generated automatically.
+]]>
+
+
+ doi: 10.1093/bioinformatics/bts635
+
+
diff -r 000000000000 -r e4b87a00b1df data_manager_conf.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/data_manager_conf.xml Wed Nov 23 17:55:57 2016 -0500
@@ -0,0 +1,22 @@
+
+
+
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diff -r 000000000000 -r e4b87a00b1df tool-data/all_fasta.loc.sample
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tool-data/all_fasta.loc.sample Wed Nov 23 17:55:57 2016 -0500
@@ -0,0 +1,18 @@
+#This file lists the locations and dbkeys of all the fasta files
+#under the "genome" directory (a directory that contains a directory
+#for each build). The script extract_fasta.py will generate the file
+#all_fasta.loc. This file has the format (white space characters are
+#TAB characters):
+#
+#
+#
+#So, all_fasta.loc could look something like this:
+#
+#apiMel3 apiMel3 Honeybee (Apis mellifera): apiMel3 /path/to/genome/apiMel3/apiMel3.fa
+#hg19canon hg19 Human (Homo sapiens): hg19 Canonical /path/to/genome/hg19/hg19canon.fa
+#hg19full hg19 Human (Homo sapiens): hg19 Full /path/to/genome/hg19/hg19full.fa
+#
+#Your all_fasta.loc file should contain an entry for each individual
+#fasta file. So there will be multiple fasta files for each build,
+#such as with hg19 above.
+#
diff -r 000000000000 -r e4b87a00b1df tool-data/rnastar_index.loc.sample
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tool-data/rnastar_index.loc.sample Wed Nov 23 17:55:57 2016 -0500
@@ -0,0 +1,38 @@
+#This is a sample file distributed with Galaxy that enables tools
+#to use a directory of BWA indexed sequences data files. You will need
+#to create these data files and then create a bwa_index.loc file
+#similar to this one (store it in this directory) that points to
+#the directories in which those files are stored. The bwa_index.loc
+#file has this format (longer white space characters are TAB characters):
+#
+#
+#
+#So, for example, if you had phiX indexed stored in
+#/depot/data2/galaxy/phiX/base/,
+#then the bwa_index.loc entry would look like this:
+#
+#phiX174 phiX phiX Pretty /depot/data2/galaxy/phiX/base/phiX.fa
+#
+#and your /depot/data2/galaxy/phiX/base/ directory
+#would contain phiX.fa.* files:
+#
+#-rw-r--r-- 1 james universe 830134 2005-09-13 10:12 phiX.fa.amb
+#-rw-r--r-- 1 james universe 527388 2005-09-13 10:12 phiX.fa.ann
+#-rw-r--r-- 1 james universe 269808 2005-09-13 10:12 phiX.fa.bwt
+#...etc...
+#
+#Your bwa_index.loc file should include an entry per line for each
+#index set you have stored. The "file" in the path does not actually
+#exist, but it is the prefix for the actual index files. For example:
+#
+#phiX174 phiX phiX174 /depot/data2/galaxy/phiX/base/phiX.fa
+#hg18canon hg18 hg18 Canonical /depot/data2/galaxy/hg18/base/hg18canon.fa
+#hg18full hg18 hg18 Full /depot/data2/galaxy/hg18/base/hg18full.fa
+#/orig/path/hg19.fa hg19 hg19 /depot/data2/galaxy/hg19/base/hg19.fa
+#...etc...
+#
+#Note that for backwards compatibility with workflows, the unique ID of
+#an entry must be the path that was in the original loc file, because that
+#is the value stored in the workflow for that parameter. That is why the
+#hg19 entry above looks odd. New genomes can be better-looking.
+#
diff -r 000000000000 -r e4b87a00b1df tool_data_table_conf.xml.sample
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_data_table_conf.xml.sample Wed Nov 23 17:55:57 2016 -0500
@@ -0,0 +1,12 @@
+
+
+