Mercurial > repos > bgruening > trim_galore
view trim_galore_wrapper.xml @ 0:3c1664caa8e3 draft
Uploaded
| author | bgruening |
|---|---|
| date | Sat, 06 Jul 2013 09:52:23 -0400 |
| parents | |
| children | 898db63d2e84 |
line wrap: on
line source
<tool id="trim_galore" name="Trim Galore" version="0.2.4.1"> <!-- Wrapper compatible with Trim Galore version 0.2.4.0 --> <description>adaptive quality and adapter trimmer</description> <version_command interpreter="perl">trim_galore --version</version_command> <requirements> <requirement type="package" version="1.1">cutadapt</requirement> <requirement type="package" version="0.10.1">fastqc</requirement> </requirements> <command interpreter="perl"> #from glob import glob #import tempfile, os trim_galore ## ## Input parameters ## #if $params.settingsType == "custom": $params.fastqc ## default 20 --quality $params.quality ## default 'AGATCGGAAGAGC' #if $params.adapter.strip() != '': --adapter $params.adapter #end if ## default 1 --stringency $params.stringency ## default 0.1 -e $params.error_rate ## default 20 --length $params.min_length #if $params.retain_unpaired.settingsType == "retain_unpaired_output": --retain_unpaired --length_1 $params.retain_unpaired.length_1 --length_2 $params.retain_unpaired.length_2 #end if #end if ## ## RBBS specific options. ## #if $rrbs.settingsType == "custom": $rrbs.rrbs $rrbs.non_directional #end if ## ## Creating a temporary directory where trim_galore will store all result files ## #set $temp_dir = os.path.abspath(tempfile.mkdtemp()) --output_dir $temp_dir --suppress_warn #if $singlePaired.sPaired == "single": #if $singlePaired.input_singles.ext == "fastqillumina": --phred64 #elif $singlePaired.input_singles.ext == "fastqsanger": --phred33 #end if #if $params.settingsType == "custom": #if not $params.report: --no_report_file #end if #end if ## input sequence $singlePaired.input_singles #else: --paired #if $singlePaired.input_mate1.ext == "fastqillumina": --phred64 #elif $singlePaired.input_mate1.ext == "fastqsanger": --phred33 #end if $singlePaired.trim1 #if $singlePaired.adapter2.strip() != '': --adapter2 $singlePaired.adapter2 #end if #if $params.settingsType == "custom": #if not $params.report: --no_report_file #end if #end if ## input sequences $singlePaired.input_mate1 $singlePaired.input_mate2 #end if && ## ## Trim Galore! run is finished. Move the result files to the proper place ## #if $singlePaired.sPaired == "single": #set $single_end_path = os.path.join($temp_dir, os.path.basename(str($singlePaired.input_singles)) + '_trimmed.fq') mv $single_end_path $trimmed_reads_single; #if $params.settingsType == "custom": #if $params.report: #set $report_path = os.path.join($temp_dir, os.path.basename(str($singlePaired.input_singles)) + '_trimming_report.txt') mv $report_path $report_file; #end if #end if #else: #set $paired_end_path_1 = os.path.join($temp_dir, os.path.basename(str($singlePaired.input_mate1)) + '_val_1.fq') #set $paired_end_path_2 = os.path.join($temp_dir, os.path.basename(str($singlePaired.input_mate2)) + '_val_2.fq') mv $paired_end_path_1 $trimmed_reads_pair1; mv $paired_end_path_2 $trimmed_reads_pair2; #if $params.settingsType == "custom": #if $params.retain_unpaired.settingsType == "retain_unpaired_output": #set $unpaired_path_1 = os.path.join($temp_dir, os.path.basename(str($singlePaired.input_mate1)) + '_unpaired_1.fq') #set $unpaired_path_2 = os.path.join($temp_dir, os.path.basename(str($singlePaired.input_mate2)) + '_unpaired_2.fq') mv $unpaired_path_1 $unpaired_reads_1; mv $unpaired_path_2 $unpaired_reads_2; #end if #if $params.report: #set $report_path = os.path.join($temp_dir, os.path.basename(str($singlePaired.input_mate1)) + '_trimming_report.txt') mv $report_path $report_file; #end if #end if #end if ## delete the temp_dir rm -rf $temp_dir </command> <inputs> <!-- Input Parameters --> <conditional name="singlePaired"> <param name="sPaired" type="select" label="Is this library mate-paired?"> <option value="single">Single-end</option> <option value="paired">Paired-end</option> </param> <when value="single"> <param name="input_singles" type="data" format="fastqsanger,fastqillumina,fastq,fasta" label="FASTQ/FASTA file" help="FASTQ or FASTA files." /> </when> <when value="paired"> <param name="input_mate1" type="data" format="fastqsanger,fastqillumina,fastq,fasta" label="FASTQ/FASTA file" help="FASTQ or FASTA files." /> <param name="input_mate2" type="data" format="fastqsanger,fastqillumina,fastq,fasta" label="FASTQ/FASTA file" help="FASTQ or FASTA files." /> <param name="trim1" type="boolean" truevalue="--trim1" falsevalue="" checked="False" label="Trims 1 bp off every read from its 3' end." help="" /> <param name="adapter2" type="text" value="" label="Optional adapter sequence to be trimmed off read 2"> <validator type="regex" message="Adapter sequence must contain DNA characters only (A,C,T,G or N)">^[ACTGNactgn]*$</validator> </param> </when> </conditional> <conditional name="params"> <param name="settingsType" type="select" label="Trim galore! advanced settings" help="You can use the default settings or set custom values for any of Trim Galore's parameters."> <option value="default">Use Defaults</option> <option value="custom">Full parameter list</option> </param> <when value="default" /> <!-- Full/advanced params. --> <when value="custom"> <param name="fastqc" type="boolean" truevalue="--fastqc" falsevalue="" checked="False" label="Run FastQC in the default mode on the FastQ file once trimming is complete" help="" /> <param name="quality" type="integer" value="20" label="Trim low-quality ends from reads in addition to adapter removal." help="For more information please see below." /> <param name="adapter" type="text" value="AGATCGGAAGAGC" label="Adapter sequence to be trimmed"> <validator type="regex" message="Adapter sequence must contain DNA characters only (A,C,T,G or N)">^[ACTGNactgn]*$</validator> </param> <param name="stringency" type="integer" value="1" label="Overlap with adapter sequence required to trim a sequence" /> <param name="error_rate" type="float" value="0.1" label="Maximum allowed error rate" /> <param name="min_length" type="integer" value="20" label="Discard reads that became shorter than length INT" /> <param name="report" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Generate a report file" help="" /> <conditional name="retain_unpaired"> <param name="settingsType" type="select" label="specify if you would like to retain unpaired reads"> <option value="no_output">Do not output unpaired reads</option> <option value="retain_unpaired_output">Output unpaired reads</option> </param> <when value="no_output" /> <!-- Output params. --> <when value="retain_unpaired_output"> <param name="length_1" type="integer" value="35" label="Unpaired single-end read length cutoff needed for read 1 to be written" /> <param name="length_2" type="integer" value="35" label="Unpaired single-end read length cutoff needed for read 2 to be written" /> </when> <!-- output --> </conditional> <!-- retain_unpaired --> </when> <!-- full --> </conditional> <!-- params --> <conditional name="rrbs"> <param name="settingsType" type="select" label="RRBS specific settings"> <option value="default">Use Defaults (no RRBS)</option> <option value="custom">Full parameter list</option> </param> <when value="default" /> <!-- Full/advanced params. --> <when value="custom"> <param name="rrbs" type="boolean" truevalue="--rrbs" falsevalue="" checked="True" label="Specifies that the input file was an MspI digested RRBS sample" /> <param name="non_directional" type="boolean" truevalue="--non_directional" falsevalue="" checked="False" label="Selecting this option for non-directional RRBS libraries" /> </when> <!-- full --> </conditional> <!-- params --> </inputs> <outputs> <data format="fastq" name="trimmed_reads_single" label="${tool.name} on ${on_string}: trimmed reads"> <filter>singlePaired['sPaired'] == "single"</filter> <actions> <action type="format"> <option type="from_param" name="singlePaired.input_singles" param_attribute="ext" /> </action> </actions> </data> <data format="fastq" name="trimmed_reads_pair1" label="${tool.name} on ${on_string}: trimmed reads pair 1"> <filter>singlePaired['sPaired'] == "paired"</filter> <actions> <action type="format"> <option type="from_param" name="singlePaired.input_mate1" param_attribute="ext" /> </action> </actions> </data> <data format="fastq" name="trimmed_reads_pair2" label="${tool.name} on ${on_string}: trimmed reads pair 2"> <filter>singlePaired['sPaired'] == "paired"</filter> <actions> <action type="format"> <option type="from_param" name="singlePaired.input_mate1" param_attribute="ext" /> </action> </actions> </data> <data format="fastq" name="unpaired_reads_1" label="${tool.name} on ${on_string}: unpaired reads (1)"> <filter> (( params['settingsType'] == "custom" and params['retain_unpaired']['settingsType'] == "retain_unpaired_output" )) </filter> <actions> <action type="format"> <option type="from_param" name="singlePaired.input_mate1" param_attribute="ext" /> </action> </actions> </data> <data format="fastq" name="unpaired_reads_2" label="${tool.name} on ${on_string}: unpaired reads (2)"> <filter> (( params['settingsType'] == "custom" and params['retain_unpaired']['settingsType'] == "retain_unpaired_output" )) </filter> <actions> <action type="format"> <option type="from_param" name="singlePaired.input_mate1" param_attribute="ext" /> </action> </actions> </data> <data format="txt" name="report_file" label="${tool.name} on ${on_string}: report file"> <filter> (( params['settingsType'] == "custom" and params['report'] == True )) </filter> </data> </outputs> <tests> </tests> <help> **What it does** TrimGalore!_ is a wrapper script that makes use of the publically available adapter trimming tool Cutadapt and FastQC for optional quality control once the trimming process has completed. .. _TrimGalore!: http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/ It is developed by Krueger F at the Babraham Institute. ------ **Know what you are doing** .. class:: warningmark There is no such thing (yet) as an automated gearshift in short read mapping. It is all like stick-shift driving in San Francisco. In other words = running this tool with default parameters will probably not give you meaningful results. A way to deal with this is to **understand** the parameters by carefully reading the `documentation`__ and experimenting. Fortunately, Galaxy makes experimenting easy. .. __: http://www.bioinformatics.babraham.ac.uk/projects/bismark/ ------ **Input formats** Bismark accepts files in either Sanger FASTQ format (galaxy type *fastqsanger*), Illumina FASTQ format (galaxy type *fastqillumina*) or FASTA format (galaxy type *fasta*). Use the FASTQ Groomer to prepare your files. ------ **A Note on Built-in Reference Genomes** The default variant for all genomes is "Full", defined as all primary chromosomes (or scaffolds/contigs) including mitochondrial plus associated unmapped, plasmid, and other segments. When only one version of a genome is available in this tool, it represents the default "Full" variant. Some genomes will have more than one variant available. The "Canonical Male" or sometimes simply "Canonical" variant contains the primary chromosomes for a genome. For example a human "Canonical" variant contains chr1-chr22, chrX, chrY, and chrM. The "Canonical Female" variant contains the primary chromosomes excluding chrY. ------ The final output of Bismark is in SAM format by default. **Outputs** The output is in SAM format, and has the following columns:: Column Description -------- -------------------------------------------------------- 1 QNAME seq-ID 2 FLAG this flag tries to take the strand a bisulfite read originated from into account (this is different from ordinary DNA alignment flags!) 3 RNAME chromosome 4 POS start position 5 MAPQ always 255 6 CIGAR extended CIGAR string 7 MRNM Mate Reference sequence NaMe ('=' if same as RNAME) 8 MPOS 1-based Mate POSition 9 ISIZE Inferred insert SIZE 10 SEQ query SEQuence on the same strand as the reference 11 QUAL Phred33 scale 12 NM-tag edit distance to the reference) 13 XX-tag base-by-base mismatches to the reference. This does not include indels. 14 XM-tag methylation call string 15 XR-tag read conversion state for the alignment 16 XG-tag genome conversion state for the alignment Each read of paired-end alignments is written out in a separate line in the above format. It looks like this (scroll sideways to see the entire example):: QNAME FLAG RNAME POS MAPQ CIAGR MRNM MPOS ISIZE SEQ QUAL OPT HWI-EAS91_1_30788AAXX:1:1:1761:343 4 * 0 0 * * 0 0 AAAAAAANNAAAAAAAAAAAAAAAAAAAAAAAAAAACNNANNGAGTNGNNNNNNNGCTTCCCACAGNNCTGG hhhhhhh;;hhhhhhhhhhh^hOhhhhghhhfhhhgh;;h;;hhhh;h;;;;;;;hhhhhhghhhh;;Phhh HWI-EAS91_1_30788AAXX:1:1:1578:331 4 * 0 0 * * 0 0 GTATAGANNAATAAGAAAAAAAAAAATGAAGACTTTCNNANNTCTGNANNNNNNNTCTTTTTTCAGNNGTAG hhhhhhh;;hhhhhhhhhhhhhhhhhhhhhhhhhhhh;;h;;hhhh;h;;;;;;;hhhhhhhhhhh;;hhVh ------- **Bismark settings** All of the options have a default value. You can change any of them. If any Bismark function is missing please contact the tool author or your Galaxy admin. ------ **Bismark parameter list** This is an exhaustive list of Bismark options: ------ **OPTIONS** Input:: --singles A comma- or space-separated list of files containing the reads to be aligned (e.g. lane1.fq,lane2.fq lane3.fq). Reads may be a mix of different lengths. Bismark will produce one mapping result and one report file per input file. -1 mates1 Comma-separated list of files containing the #1 mates (filename usually includes "_1"), e.g. flyA_1.fq,flyB_1.fq). Sequences specified with this option must correspond file-for-file and read-for-read with those specified in mates2. Reads may be a mix of different lengths. Bismark will produce one mapping result and one report file per paired-end input file pair. -2 mates2 Comma-separated list of files containing the #2 mates (filename usually includes "_2"), e.g. flyA_1.fq,flyB_1.fq). Sequences specified with this option must correspond file-for-file and read-for-read with those specified in mates1. Reads may be a mix of different lengths. -q/--fastq The query input files (specified as mate1,mate2 or singles are FASTQ files (usually having extension .fg or .fastq). This is the default. See also --solexa-quals. -f/--fasta The query input files (specified as mate1,mate2 or singles are FASTA files (usually havin extension .fa, .mfa, .fna or similar). All quality values are assumed to be 40 on the Phred scale. -s/--skip INT Skip (i.e. do not align) the first INT reads or read pairs from the input. -u/--upto INT Only aligns the first INT reads or read pairs from the input. Default: no limit. --phred33-quals FASTQ qualities are ASCII chars equal to the Phred quality plus 33. Default: on. --phred64-quals FASTQ qualities are ASCII chars equal to the Phred quality plus 64. Default: off. --solexa-quals Convert FASTQ qualities from solexa-scaled (which can be negative) to phred-scaled (which can't). The formula for conversion is: phred-qual = 10 * log(1 + 10 ** (solexa-qual/10.0)) / log(10). Used with -q. This is usually the right option for use with (unconverted) reads emitted by the GA Pipeline versions prior to 1.3. Works only for Bowtie 1. Default: off. --solexa1.3-quals Same as --phred64-quals. This is usually the right option for use with (unconverted) reads emitted by GA Pipeline version 1.3 or later. Default: off. Alignment:: -n/--seedmms INT The maximum number of mismatches permitted in the "seed", i.e. the first L base pairs of the read (where L is set with -l/--seedlen). This may be 0, 1, 2 or 3 and the default is 1. This option is only available for Bowtie 1 (for Bowtie 2 see -N). -l/--seedlen The "seed length"; i.e., the number of bases of the high quality end of the read to which the -n ceiling applies. The default is 28. Bowtie (and thus Bismark) is faster for larger values of -l. This option is only available for Bowtie 1 (for Bowtie 2 see -L). -e/--maqerr INT Maximum permitted total of quality values at all mismatched read positions throughout the entire alignment, not just in the "seed". The default is 70. Like Maq, bowtie rounds quality values to the nearest 10 and saturates at 30. This value is not relevant for Bowtie 2. --chunkmbs INT The number of megabytes of memory a given thread is given to store path descriptors in --best mode. Best-first search must keep track of many paths at once to ensure it is always extending the path with the lowest cumulative cost. Bowtie tries to minimize the memory impact of the descriptors, but they can still grow very large in some cases. If you receive an error message saying that chunk memory has been exhausted in --best mode, try adjusting this parameter up to dedicate more memory to the descriptors. This value is not relevant for Bowtie 2. Default: 512. -I/--minins INT The minimum insert size for valid paired-end alignments. E.g. if -I 60 is specified and a paired-end alignment consists of two 20-bp alignments in the appropriate orientation with a 20-bp gap between them, that alignment is considered valid (as long as -X is also satisfied). A 19-bp gap would not be valid in that case. Default: 0. -X/--maxins INT The maximum insert size for valid paired-end alignments. E.g. if -X 100 is specified and a paired-end alignment consists of two 20-bp alignments in the proper orientation with a 60-bp gap between them, that alignment is considered valid (as long as -I is also satisfied). A 61-bp gap would not be valid in that case. Default: 500. Output:: --non_directional The sequencing library was constructed in a non strand-specific manner, alignments to all four bisulfite strands will be reported. Default: OFF. (The current Illumina protocol for BS-Seq is directional, in which case the strands complementary to the original strands are merely theoretical and should not exist in reality. Specifying directional alignments (which is the default) will only run 2 alignment threads to the original top (OT) or bottom (OB) strands in parallel and report these alignments. This is the recommended option for sprand-specific libraries). --sam-no-hd Suppress SAM header lines (starting with @). This might be useful when very large input files are split up into several smaller files to run concurrently and the output files are to be merged. --quiet Print nothing besides alignments. --vanilla Performs bisulfite mapping with Bowtie 1 and prints the 'old' output (as in Bismark 0.5.X) instead of SAM format output. -un/--unmapped Write all reads that could not be aligned to a file in the output directory. Written reads will appear as they did in the input, without any translation of quality values that may have taken place within Bowtie or Bismark. Paired-end reads will be written to two parallel files with _1 and _2 inserted in their filenames, i.e. _unmapped_reads_1.txt and unmapped_reads_2.txt. Reads with more than one valid alignment with the same number of lowest mismatches (ambiguous mapping) are also written to _unmapped_reads.txt unless the option --ambiguous is specified as well. --ambiguous Write all reads which produce more than one valid alignment with the same number of lowest mismatches or other reads that fail to align uniquely to a file in the output directory. Written reads will appear as they did in the input, without any of the translation of quality values that may have taken place within Bowtie or Bismark. Paired-end reads will be written to two parallel files with _1 and _2 inserted in theit filenames, i.e. _ambiguous_reads_1.txt and _ambiguous_reads_2.txt. These reads are not written to the file specified with --un. -o/--output_dir DIR Write all output files into this directory. By default the output files will be written into the same folder as the input file(s). If the specified folder does not exist, Bismark will attempt to create it first. The path to the output folder can be either relative or absolute. --temp_dir DIR Write temporary files to this directory instead of into the same directory as the input files. If the specified folder does not exist, Bismark will attempt to create it first. The path to the temporary folder can be either relative or absolute. ------ Bowtie 2 alignment options:: -N INT Sets the number of mismatches to allowed in a seed alignment during multiseed alignment. Can be set to 0 or 1. Setting this higher makes alignment slower (often much slower) but increases sensitivity. Default: 0. This option is only available for Bowtie 2 (for Bowtie 1 see -n). -L INT Sets the length of the seed substrings to align during multiseed alignment. Smaller values make alignment slower but more senstive. Default: the --sensitive preset of Bowtie 2 is used by default, which sets -L to 20. This option is only available for Bowtie 2 (for Bowtie 1 see -l). --ignore-quals When calculating a mismatch penalty, always consider the quality value at the mismatched position to be the highest possible, regardless of the actual value. I.e. input is treated as though all quality values are high. This is also the default behavior when the input doesn't specify quality values (e.g. in -f mode). This option is invariable and on by default. Bowtie 2 paired-end options:: --no-mixed This option disables Bowtie 2's behavior to try to find alignments for the individual mates if it cannot find a concordant or discordant alignment for a pair. This option is invariable and and on by default. --no-discordant Normally, Bowtie 2 looks for discordant alignments if it cannot find any concordant alignments. A discordant alignment is an alignment where both mates align uniquely, but that does not satisfy the paired-end constraints (--fr/--rf/--ff, -I, -X). This option disables that behavior and it is on by default. Bowtie 2 effort options:: -D INT Up to INT consecutive seed extension attempts can "fail" before Bowtie 2 moves on, using the alignments found so far. A seed extension "fails" if it does not yield a new best or a new second-best alignment. Default: 15. -R INT INT is the maximum number of times Bowtie 2 will "re-seed" reads with repetitive seeds. When "re-seeding," Bowtie 2 simply chooses a new set of reads (same length, same number of mismatches allowed) at different offsets and searches for more alignments. A read is considered to have repetitive seeds if the total number of seed hits divided by the number of seeds that aligned at least once is greater than 300. Default: 2. Bowtie 2 Scoring options:: --score_min "func" Sets a function governing the minimum alignment score needed for an alignment to be considered "valid" (i.e. good enough to report). This is a function of read length. For instance, specifying L,0,-0.2 sets the minimum-score function f to f(x) = 0 + -0.2 * x, where x is the read length. See also: setting function options at http://bowtie-bio.sourceforge.net/bowtie2. The default is L,0,-0.2. Bowtie 2 Reporting options:: --most_valid_alignments INT This used to be the Bowtie 2 parameter -M. As of Bowtie 2 version 2.0.0 beta7 the option -M is deprecated. It will be removed in subsequent versions. What used to be called -M mode is still the default mode, but adjusting the -M setting is deprecated. Use the -D and -R options to adjust the effort expended to find valid alignments. For reference, this used to be the old (now deprecated) description of -M: Bowtie 2 searches for at most INT+1 distinct, valid alignments for each read. The search terminates when it can't find more distinct valid alignments, or when it finds INT+1 distinct alignments, whichever happens first. Only the best alignment is reported. Information from the other alignments is used to estimate mapping quality and to set SAM optional fields, such as AS:i and XS:i. Increasing -M makes Bowtie 2 slower, but increases the likelihood that it will pick the correct alignment for a read that aligns many places. For reads that have more than INT+1 distinct, valid alignments, Bowtie 2 does not guarantee that the alignment reported is the best possible in terms of alignment score. -M is always used and its default value is set to 10. </help> </tool>