# HG changeset patch
# User iuc
# Date 1649160668 0
# Node ID e6799e98c5fbed60fef21fb0a24c6c2b2a7acb46

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/blast commit 15fc6c06f743bae276ff02dc405e7da61a07bd08"

diff -r 000000000000 -r e6799e98c5fb macros.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/macros.xml	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,33 @@
+<macros>
+    <token name="@TOOL_VERSION@">1.6.0</token>
+    <token name="@VERSION_SUFFIX@">0</token>
+    <token name="@PROFILE@">20.09</token>
+    <xml name="requirements">
+        <requirements>
+            <requirement type="package" version="@TOOL_VERSION@">magicblast</requirement>
+            <requirement type="package" version="1.15">samtools</requirement>
+        </requirements>
+    </xml>
+    <xml name="output_sort_param">
+        <param name="output_sort" type="select" label="BAM sorting mode" help="The 'Not sorted' option can significantly extend the run time of the tool (it runs using a single thread)">
+            <option value="coordinate" selected="True">Sort by chromosomal coordinates</option>
+            <option value="name">Sort by read names</option>
+            <option value="unsorted">Not sorted (sorted as input)</option>
+        </param>
+    </xml>
+    <xml name="sanitize_query" token_validinitial="string.ascii_letters,string.digits,string.whitespace,string.punctuation">
+        <sanitizer>
+            <valid initial="@VALIDINITIAL@">
+                <remove value="&apos;"/>
+            </valid>
+            <mapping initial="none">
+                <add source="&apos;" target="&apos;&quot;&apos;&quot;&apos;"/>
+            </mapping>
+        </sanitizer>
+    </xml>
+    <xml name="citations">
+        <citations>
+            <citation type="doi">10.1186/s12859-019-2996-x</citation>
+        </citations>
+    </xml>
+</macros>
diff -r 000000000000 -r e6799e98c5fb magicblast.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/magicblast.xml	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,362 @@
+<tool id="magicblast" name="Magic-BLAST: map large RNA or DNA sequences" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@">
+    <description>against a whole genome or transcriptome</description>
+    <macros>
+        <import>macros.xml</import>
+    </macros>
+    <expand macro="requirements"/>
+    <command detect_errors="exit_code"><![CDATA[
+#import os
+
+magicblast
+-num_threads \${GALAXY_SLOTS:-8}
+#if $query.is_of_type('fasta.gz', 'fastqsanger.gz'):
+    -query <(gunzip -c '${query}')
+#else:
+    -query '${query}'
+#end if
+#if $query_mate:
+    -paired
+    #if $query.is_of_type('fasta.gz', 'fastqsanger.gz'):
+        -query_mate <(gunzip -c '${query}')
+    #else:
+        -query_mate '${query}'
+    #end if
+#end if
+
+#if $query.is_of_type('fastqsanger', 'fastqsanger.gz'):
+    -infmt fastq
+#end if
+
+#if $db_opts.db_opts_selector == "histdb":
+    -db '${os.path.join($db_opts.histdb.extra_files_path, "blastdb")}'
+#elif $db_opts.db_opts_selector == "db":
+    -db '${os.path.join($db_opts.database.fields.path, "blastdb")}'
+#else:
+    #if $db_opts.subject.is_of_type('fasta.gz'):
+        -subject <(gunzip -c '${$db_opts.subject}')
+    #else:
+        -subject '${db_opts.subject}'
+    #end if
+#end if
+
+## General search options
+-word_size $general_search.word_size
+-gapopen $general_search.gapopen
+-gapextend $general_search.gapextend
+-penalty $general_search.penalty
+-max_intron_length $general_search.max_intron_length
+
+## Query filtering options
+$query_filtering.lcase_masking
+-validate_seqs $query_filtering.validate_seqs
+-limit_lookup $query_filtering.limit_lookup
+-max_db_word_count $query_filtering.max_db_word_count
+-lookup_stride $query_filtering.lookup_stride
+
+## Restrict database search
+#if $restrict_search.gilist:
+    -gilist '$restrict_search.gilist'
+#end if
+#if $restrict_search.negative_gilist:
+    -negative_gilist '$restrict_search.negative_gilist'
+#end if
+#if $restrict_search.seqidlist:
+    -seqidlist '$restrict_search.seqidlist'
+#end if
+#if $restrict_search.negative_seqidlist:
+    -negative_seqidlist '$restrict_search.negative_seqidlist'
+#end if
+#if str($restrict_search.taxids) != '':
+    --taxids '$restrict_search.taxids'
+#end if
+#if $restrict_search.taxidlist:
+    -taxidlist '$restrict_search.taxidlist'
+#end if
+#if str($restrict_search.negative_taxids) != '':
+    --negative_taxids '$restrict_search.negative_taxids'
+#end if
+#if $restrict_search.negative_taxidlist:
+    -negative_taxidlist '$restrict_search.negative_taxidlist'
+#end if
+
+## Mapping options
+-score $mapping.score
+#if $mapping.max_edit_dist > 0:
+    -max_edit_dist $mapping.max_edit_dist
+#end if
+-splice '$mapping.splice'
+-reftype '$mapping.reftype'
+
+## Output unaligned options
+#if str($output_options.report_unaligned_cond.report_unaligned) == 'yes':
+    #if str($output_options.report_unaligned_cond.report_unaligned_separately_cond.report_unaligned_separately) == 'yes':
+        -out_unaligned 'out_unaligned'
+        #if str($output_options.report_unaligned_cond.report_unaligned_separately_cond.unaligned_fmt_cond.unaligned_fmt) == 'bam':
+            -unaligned_fmt 'sam'
+        #else:
+            -unaligned_fmt '$output_options.report_unaligned_cond.report_unaligned_separately_cond.unaligned_fmt_cond.unaligned_fmt'
+        #end if
+    #end if
+#else:
+    -no_unaligned
+#end if
+
+## Additional output options
+$output_options.no_discordant
+## Switch default SAM output to be BAM.
+#if str($output_options.outfmt_cond.outfmt) == 'bam':
+    $output_options.outfmt_cond.md_tag
+    #if $query_mate:
+        $output_options.outfmt_cond.no_query_id_trim
+    #end if
+    -out 'output.sam'
+    #if str($output_options.outfmt_cond.output_sort) == 'coordinate':
+        && samtools sort -@\${GALAXY_SLOTS:-4} -O bam 'output.sam' > '$output'
+    #elif str($output_options.outfmt_cond.output_sort) == 'name':
+        && samtools sort -n -@\${GALAXY_SLOTS:-4} -O bam -o 'output.sam' > '$output'
+    #else:
+        && samtools view -@\${GALAXY_SLOTS:-4} -bS 'output.sam' > '$output'
+    #end if
+#else:
+    -out '$output'
+    -outfmt '$output_options.outfmt_cond.outfmt'
+#end if
+
+## Convert out_unaligned from SAM to BAM if necessary
+
+#if str($output_options.report_unaligned_cond.report_unaligned) == 'yes':
+    #if str($output_options.report_unaligned_cond.report_unaligned_separately_cond.report_unaligned_separately) == 'yes':
+        #if str($output_options.report_unaligned_cond.report_unaligned_separately_cond.unaligned_fmt_cond.unaligned_fmt) == 'bam':
+            #if str($output_options.report_unaligned_cond.report_unaligned_separately_cond.unaligned_fmt_cond.output_sort) == 'coordinate':
+                && samtools sort -@\${GALAXY_SLOTS:-4} -O bam -o 'out_unaligned' > '$output_unaligned'
+            #elif str($output_options.report_unaligned_cond.report_unaligned_separately_cond.unaligned_fmt_cond.output_sort) == 'name':
+                && samtools sort -n -@\${GALAXY_SLOTS:-4} -O bam -o 'out_unaligned' > '$output_unaligned'
+            #else:
+                && samtools view -@\${GALAXY_SLOTS:-4} -bS 'out_unaligned' > '$output_unaligned'
+            #end if
+        #else:
+            && mv 'out_unaligned' '$output_unaligned'
+        #end if
+    #end if
+#end if
+    ]]></command>
+    <inputs>
+        <param argument="-query" type="data" format="fasta,fasta.gz,fastqsanger,fastqsanger.gz" label="Query file" help="Fasta or fastqsanger, optionally gzipped"/>
+        <param argument="-query_mate" type="data" format="fasta,fasta.gz,fastqsanger,fastqsanger.gz" optional="true" label="Query mate file (optional)" help="Fasta or fastqsanger, optionally gzipped"/>
+        <conditional name="db_opts">
+            <param name="db_opts_selector" type="select" label="Subject database/sequences">
+              <option value="histdb" selected="true">blast database from your history</option>
+              <option value="db">Locally installed blast database</option>
+              <option value="file">fasta file from your history (see warning in the tool help section below)</option>
+            </param>
+            <when value="histdb">
+                <param name="histdb" type="data" format="blastdbn" label="Nucleotide blast database"/>
+            </when>
+            <when value="db">
+                <param name="database" type="select" multiple="true" optional="false" label="Nucleotide blast database">
+                    <options from_data_table="blastdb"/>
+                </param>
+            </when>
+            <when value="file">
+                <param argument="-subject" type="data" format="fasta,fasta.gz" label="Nucleotide fasta subject file to use instead of a database"/>
+            </when>
+        </conditional>
+        <section name="general_search" title="General search">
+            <param argument="-word_size" type="integer" value="18" min="12" label="Minimum number of consecutive bases matching exactly"/>
+            <param argument="-gapopen" type="integer" value="0" min="0" label="Cost to open a gap"/>
+            <param argument="-gapextend" type="integer" value="0" min="0" label="Cost to extend a gap"/>
+            <param argument="-penalty" type="integer" value="-4" max="0" label="Penalty for a nucleotide mismatch"/>
+            <param argument="-max_intron_length" type="integer" value="500000" min="0" label="Maximum allowed intron length"/>
+        </section>
+        <section name="query_filtering" title="Query filtering">
+            <param argument="-lcase_masking" type="boolean" truevalue="-lcase_masking" falsevalue="" checked="false" label="Use lower case filtering in subject sequences?"/>
+            <param argument="-validate_seqs" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Reject low quality sequences?"/>
+            <param argument="-limit_lookup" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Remove word seeds with high frequency in the searched database?"/>
+            <param argument="-max_db_word_count" type="integer" value="30" min="0" label="Words that appear more than this number of times in the database will be masked in the lookup table"/>
+            <param argument="-lookup_stride" type="integer" value="0" min="0" label="Number of words to skip after collecting one while creating a lookup table"/>
+        </section>
+        <section name="restrict_search" title="Restrict database search">
+            <param argument="-gilist" type="data" format="tabular" optional="true" label="Tabular file containing list of GIs to which to restrict database search" help="Available only for database searches"/>
+            <param argument="-negative_gilist" type="data" format="tabular" optional="true" label="Tabular file containing list of GIs to restrict database search to everything except the specified GIs" help="Available only for database searches"/>
+            <param argument="-seqidlist" type="data" format="tabular" optional="true" label="Tabular file containing list of SeqIDs to which to restrict database search" help="Available only for database searches"/>
+            <param argument="-negative_seqidlist" type="data" format="tabular" optional="true" label="Tabular file containing list of SeqIDs to restrict database search to everything except the specified SeqIDs" help="Available only for database searches"/>
+            <param argument="-taxids" type="text" optional="true" label="Comma-separated list of taxonomy IDs to which to restrict database search" help="Available only for database searches">
+                <expand macro="sanitize_query" validinitial="string.ascii_letters,string.digits,string.whitespace,string.punctuation"/>
+            </param>
+            <param argument="-taxidlist" type="data" format="tabular" optional="true" label="Tabular file containing list of taxonomy IDs to which to restrict database search" help="Available only for database searches"/>
+            <param argument="-negative_taxids" type="text" optional="true" label="Comma-separated list of taxonomy IDs to restrict database search to everything except the specified taxonomy IDs" help="Available only for database searches">
+                <expand macro="sanitize_query" validinitial="string.ascii_letters,string.digits,string.whitespace,string.punctuation"/>
+            </param>
+            <param argument="-negative_taxidlist" type="data" format="tabular" optional="true" label="Tabular file containing list of taxonomy IDs to restrict database search to everythin except the specified taxonomy IDs" help="Available only for database searches"/>
+        </section>
+        <section name="mapping" title="Mapping">
+            <param argument="-score" type="integer" value="0" min="0" label="Cutoff score for accepting alignments" help="Zero value ignores"/>
+            <param argument="-max_edit_dist" type="integer" value="0" min="0" label="Cutoff edit distance for accepting an alignment" help="Zero value is unlimited"/>
+            <param argument="-splice" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Search for spliced alignments?"/>
+            <param argument="-reftype" type="select" label="Type of the reference">
+                <option value="genome" selected="true">genome</option>
+                <option value="transcriptome">transcriptome</option>
+            </param>
+        </section>
+        <section name="output_options" title="Output options">
+            <conditional name="report_unaligned_cond">
+                <param name="report_unaligned" type="select" label="Report unaligned reads?">
+                    <option value="yes" selected="true">Yes</option>
+                    <option value="no">No</option>
+                </param>
+                <when value="yes">
+                    <conditional name="report_unaligned_separately_cond">
+                        <param name="report_unaligned_separately" type="select" label="Output unaligned reads to a separate file?" help="Select No to output all reads to the same file">
+                            <option value="no" selected="true">No</option>
+                            <option value="yes">Yes</option>
+                        </param>
+                        <when value="no"/>
+                        <when value="yes">
+                            <conditional name="unaligned_fmt_cond">
+                                <param argument="-unaligned_fmt" type="select" label="Output format for unaligned reads">
+                                    <option value="bam" selected="true">bam</option>
+                                    <option value="tabular">tabular</option>
+                                    <option value="fasta">fasta</option>
+                                </param>
+                                <when value="bam">
+                                    <expand macro="output_sort_param"/>
+                                </when>
+                                <when value="tabular"/>
+                                <when value="fasta"/>
+                            </conditional>
+                        </when>
+                    </conditional>
+                </when>
+                <when value="no"/>
+            </conditional>
+            <conditional name="outfmt_cond">
+                <param argument="-outfmt" type="select" label="Output format">
+                    <option value="bam" selected="true">bam</option>
+                    <option value="tabular">tabular</option>
+                </param>
+                <when value="bam">
+                    <expand macro="output_sort_param"/>
+                    <param argument="-md_tag" type="boolean" truevalue="-md_tag" falsevalue="" checked="false" label="Include MD tag in BAM output?"/>
+                    <param argument="-no_query_id_trim" type="boolean" truevalue="-no_query_id_trim" falsevalue="" checked="false" label="Do not trim '.1', '/1', '.2', or '/2' at the end of read ids in BAM output for paired reads?" help="Ignored if no query mate"/>
+                </when>
+                <when value="tabular"/>
+            </conditional>
+            <param argument="-no_discordant" type="boolean" truevalue="-no_discordant" falsevalue="" checked="false" label="Suppress discordant alignments for paired reads?" help="Ignored if no query mate"/>
+        </section>
+    </inputs>
+    <outputs>
+        <data name="output" format="bam" label="${tool.name} on ${on_string}">
+            <change_format>
+                <when input="output.outfmt_cond.outfmt" value="tabular" format="tabular"/>
+            </change_format>
+        </data>
+        <data name="output_unaligned" format="bam" label="${tool.name} on ${on_string}: unaligned reads">
+            <filter>output_options['report_unaligned_cond']['report_unaligned'] == 'yes' and output_options['report_unaligned_cond']['report_unaligned_separately_cond']['report_unaligned_separately'] == 'yes'</filter>
+            <change_format>
+                <when input="output_options.report_unaligned_cond.report_unaligned_separately_cond.unaligned_fmt_cond.unaligned_fmt" value="tabular" format="tabular"/>
+                <when input="output_options.report_unaligned_cond.report_unaligned_separately_cond.unaligned_fmt_cond.unaligned_fmt" value="fasta" format="fasta"/>
+            </change_format>
+        </data>
+    </outputs>
+    <tests>
+        <!-- Single fasta.gz input, subject file -->
+        <test expect_num_outputs="1">
+            <param name="query" value="query1.fasta.gz" ftype="fasta.gz"/>
+            <param name="db_opts_selector" value="file"/>
+            <param name="subject" value="subject1.fasta.gz" ftype="fasta.gz"/>
+            <output name="output" ftype="bam">
+                <assert_contents>
+                    <has_size value="1247" delta="50"/>
+                </assert_contents>
+            </output>
+        </test>
+        <!-- Single fasta.gz input, subject file, output unaligned reads separately-->
+        <test expect_num_outputs="2">
+            <param name="query" value="query1.fasta.gz" ftype="fasta.gz"/>
+            <param name="db_opts_selector" value="file"/>
+            <param name="subject" value="subject1.fasta.gz" ftype="fasta.gz"/>
+            <param name="report_unaligned_separately" value="yes"/>
+            <param name="unaligned_fmt" value="tabular"/>
+            <output name="output" ftype="bam">
+                <assert_contents>
+                    <has_size value="492" delta="50"/>
+                </assert_contents>
+            </output>
+            <output name="output_unaligned" ftype="tabular">
+                <assert_contents>
+                    <has_size value="959"/>
+                </assert_contents>
+            </output>
+        </test>
+        <!-- Single fasta.gz input, subject file, gilist file, results in error -->
+        <test expect_failure="true">
+            <param name="query" value="query1.fasta.gz" ftype="fasta.gz"/>
+            <param name="db_opts_selector" value="file"/>
+            <param name="subject" value="subject1.fasta.gz" ftype="fasta.gz"/>
+            <param name="report_unaligned_separately" value="yes"/>
+            <param name="gilist" value="gilist1.tabular" ftype="tabular"/>
+            <assert_stderr>
+                <has_text text="Incompatible with argument:"/>
+            </assert_stderr>
+        </test>
+        <!-- Single fasta.gz input, cached db, taxidlist, results in error -->
+        <test expect_failure="true">
+            <param name="query" value="query1.fasta.gz" ftype="fasta.gz"/>
+            <param name="db_opts_selector" value="db"/>
+            <param name="database" value="phiX174"/>
+            <param name="taxidlist" value="taxids.tabular" ftype="tabular"/>
+            <assert_stderr>
+                <has_text text="Taxonomy filtering is not supported in v4 BLAST dbs"/>
+            </assert_stderr>
+        </test>
+        <!-- Paired fastqsanger.gz input, subject file -->
+        <test expect_num_outputs="1">
+            <param name="query" value="query_forward1.fastqsanger.gz" ftype="fastqsanger.gz"/>
+            <param name="query_mate" value="query_reverse1.fastqsanger.gz" ftype="fastqsanger.gz"/>
+            <param name="db_opts_selector" value="file"/>
+            <param name="subject" value="subject1.fasta.gz" ftype="fasta.gz"/>
+            <output name="output" ftype="bam">
+                <assert_contents>
+                    <has_size value="62080" delta="50"/>
+                </assert_contents>
+            </output>
+        </test>
+        <!-- Paired fastqsanger.gz input, cached blast db -->
+        <test expect_num_outputs="1">
+            <param name="query" value="query_forward1.fastqsanger.gz" ftype="fastqsanger.gz"/>
+            <param name="query_mate" value="query_reverse1.fastqsanger.gz" ftype="fastqsanger.gz"/>
+            <param name="db_opts_selector" value="db"/>
+            <param name="database" value="phiX174"/>
+            <output name="output" ftype="bam">
+                <assert_contents>
+                    <has_size value="62079" delta="50"/>
+                </assert_contents>
+            </output>
+        </test>
+    </tests>
+    <help><![CDATA[
+**What it does**
+
+.. class:: warningmark
+
+In addition to a BLAST database, you can also search against a fasta file of subject (target) sequences. However, this is not
+advised because it is slower (only one CPU is used), but more importantly gives e-values for pairwise searches (very small
+e-values which will look overly signficiant).  In most cases you should convert the fasta file into a blast database using
+*makeblastdb* and search against that.
+
+Magic-BLAST is a tool for mapping large next-generation RNA or DNA sequencing runs against a whole genome or transcriptome.
+Each alignment optimizes a composite score, taking into account simultaneously the two reads of a pair, and in case of RNA-seq,
+locating the candidate introns and adding up the score of all exons. This is very different from other versions of BLAST, where
+each exon is scored as a separate hit and read-pairing is ignored.
+
+Magic-BLAST incorporates within the NCBI BLAST code framework ideas developed in the NCBI Magic pipeline, in particular hit
+extensions by local walk and jump, and recursive clipping of mismatches near the edges of the reads, which avoids accumulating
+artefactual mismatches near splice sites and is needed to distinguish short indels from substitutions near the edges.
+
+The tool accepts a single or paired set of reads in fasta or fastqsanger format and produces bam or tabular output.
+
+More information about Magic-BLAST is available in the
+`online documentation <https://ncbi.github.io/magicblast/>`_.
+    ]]></help>
+    <expand macro="citations"/>
+</tool>
diff -r 000000000000 -r e6799e98c5fb test-data/blastdb.loc
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/blastdb.loc	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,4 @@
+# This file is just a placeholder since Galxy does
+# not yet suppoort uploading a BLAST database, which
+# is required for functional tests.
+phiX174	phiX174	${__HERE__}/phiX174
diff -r 000000000000 -r e6799e98c5fb test-data/gilist1.tabular
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/gilist1.tabular	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,1 @@
+57163782
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nhd
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phiX174/blastdb.nhd	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,7 @@
+15495040301
+25770063902
+2660043075
+27122163083
+3427376816
+40885395164
+7819003870
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nhi
Binary file test-data/phiX174/blastdb.nhi has changed
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nhr
Binary file test-data/phiX174/blastdb.nhr has changed
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nin
Binary file test-data/phiX174/blastdb.nin has changed
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nog
Binary file test-data/phiX174/blastdb.nog has changed
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nsd
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phiX174/blastdb.nsd	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,7 @@
+gnl|bl_ord_id|00
+gnl|bl_ord_id|11
+gnl|bl_ord_id|22
+gnl|bl_ord_id|33
+gnl|bl_ord_id|44
+gnl|bl_ord_id|55
+gnl|bl_ord_id|66
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nsi
Binary file test-data/phiX174/blastdb.nsi has changed
diff -r 000000000000 -r e6799e98c5fb test-data/phiX174/blastdb.nsq
Binary file test-data/phiX174/blastdb.nsq has changed
diff -r 000000000000 -r e6799e98c5fb test-data/query1.fasta.gz
Binary file test-data/query1.fasta.gz has changed
diff -r 000000000000 -r e6799e98c5fb test-data/query_forward1.fastqsanger.gz
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diff -r 000000000000 -r e6799e98c5fb test-data/query_reverse1.fastqsanger.gz
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diff -r 000000000000 -r e6799e98c5fb test-data/taxids.tabular
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/taxids.tabular	Tue Apr 05 12:11:08 2022 +0000
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+57163782
diff -r 000000000000 -r e6799e98c5fb tool-data/blastdb.loc.sample
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool-data/blastdb.loc.sample	Tue Apr 05 12:11:08 2022 +0000
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+# This is a sample file distributed with Galaxy that is used to define a
+# list of nucleotide BLAST databases, using three columns tab separated:
+#
+# <unique_id>{tab}<database_caption>{tab}<base_name_path>
+#
+# The captions typically contain spaces and might end with the build date.
+# It is important that the actual database name does not have a space in
+# it, and that there are only two tabs on each line.
+#
+# You can download the NCBI provided protein databases like NR from here:
+# ftp://ftp.ncbi.nlm.nih.gov/blast/db/
+#
+# For simplicity, many Galaxy servers are configured to offer just a live
+# version of each NCBI BLAST database (updated with the NCBI provided
+# Perl scripts or similar). In this case, we recommend using the case
+# sensistive base-name of the NCBI BLAST databases as the unique id.
+# Consistent naming is important for sharing workflows between Galaxy
+# servers.
+#
+# For example, consider the NCBI partially non-redundant nucleotide 
+# nt BLAST database, where you have downloaded and decompressed the
+# files under /data/blastdb/ meaning at the command line BLAST+ would
+# would look at the files /data/blastdb/nt.n* when run with:
+#
+# $ blastn -db /data/blastdb/nt -query ...
+#
+# In this case use nr (lower case to match the NCBI file naming) as the
+# unique id in the first column of blastdb_p.loc, giving an entry like
+# this:
+#
+# nt{tab}NCBI partially non-redundant (nt){tab}/data/blastdb/nt
+#
+# Alternatively, rather than a "live" mirror of the NCBI databases which
+# are updated automatically, for full reproducibility the Galaxy Team
+# recommend saving date-stamped copies of the databases. In this case
+# your blastdb.loc file should include an entry per line for each
+# version you have stored. For example:
+#
+# nt_05Jun2010{tab}NCBI nt (partially non-redundant) 05 Jun 2010{tab}/data/blastdb/05Jun2010/nt
+# nt_15Aug2010{tab}NCBI nt (partially non-redundant) 15 Aug 2010{tab}/data/blastdb/15Aug2010/nt
+# ...etc...
+#
+# See also blastdb_p.loc which is for any protein BLAST database, and
+# blastdb_d.loc which is for any protein domains databases (like CDD).
diff -r 000000000000 -r e6799e98c5fb tool_data_table_conf.xml.sample
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_data_table_conf.xml.sample	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,6 @@
+<tables>
+    <table name="blastdb" comment_char="#" allow_duplicate_entries="False">
+        <columns>value, name, path</columns>
+        <file path="tool-data/blastdb.loc"/>
+    </table>
+</tables>
diff -r 000000000000 -r e6799e98c5fb tool_data_table_conf.xml.test
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_data_table_conf.xml.test	Tue Apr 05 12:11:08 2022 +0000
@@ -0,0 +1,6 @@
+<tables>
+    <table name="blastdb" comment_char="#" allow_duplicate_entries="False">
+        <columns>value, name, path</columns>
+        <file path="${__HERE__}/test-data/blastdb.loc"/>
+    </table>
+</tables>