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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/fastplong commit e42ea8cb63b6c98b7f782a26ab0fe5b3e50d2275
| author | iuc |
|---|---|
| date | Mon, 02 Jun 2025 10:09:02 +0000 |
| parents | 6fa648249316 |
| children |
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<tool id="fastplong" name="Fastplong" version="@TOOL_VERSION@+galaxy0" profile="23.2" license="MIT"> <description>Filter and trim long reads</description> <creator> <organization name="Masaryk University" url="https://www.muni.cz/"/> <person givenName="Hana" familyName="Resovska" email="499924@mail.muni.cz"/> </creator> <macros> <token name="@TOOL_VERSION@">0.3.0</token> </macros> <requirements> <requirement type="package" version="@TOOL_VERSION@">fastplong</requirement> </requirements> <command detect_errors="exit_code"> <![CDATA[ fastplong --thread \${GALAXY_SLOTS:-1} --report_title 'fastplong report for $in' --in '$in' --out '$output' #if $reads_to_process: --reads_to_process '$reads_to_process' #end if $disable_quality_filtering $disable_adapter_trimming #if $start_adapter: --start_adapter '$start_adapter' #end if #if $end_adapter: --end_adapter '$end_adapter' #end if #if $adapter_fasta: --adapter_fasta '$adapter_fasta' #end if #if $distance_threshold: --distance_threshold '$distance_threshold' #end if #if $trimming_extension: --trimming_extension '$trimming_extension' #end if #if $trim_front: --trim_front '$trim_front' #end if #if $trim_tail: --trim_tail '$trim_tail' #end if $trim_poly_x #if $poly_x_min_len: --poly_x_min_len '$poly_x_min_len' #end if $cut_front $cut_tail #if $cut_window_size: --cut_window_size '$cut_window_size' #end if #if $cut_mean_quality: --cut_mean_quality '$cut_mean_quality' #end if #if $cut_front_window_size: --cut_front_window_size '$cut_front_window_size' #end if #if $cut_front_mean_quality: --cut_front_mean_quality '$cut_front_mean_quality' #end if #if $cut_tail_window_size: --cut_tail_window_size '$cut_tail_window_size' #end if #if $cut_tail_mean_quality: --cut_tail_mean_quality '$cut_tail_mean_quality' #end if #if $qualified_quality_phred: --qualified_quality_phred '$qualified_quality_phred' #end if #if $unqualified_percent_limit: --unqualified_percent_limit '$unqualified_percent_limit' #end if #if $n_base_limit: --n_base_limit '$n_base_limit' #end if #if $mean_qual: --mean_qual '$mean_qual' #end if $disable_length_filtering: #if $length_required: --length_required '$length_required' #end if #if $length_limit: --length_limit '$length_limit' #end if $low_complexity_filter: #if $complexity_threshold: --complexity_threshold '$complexity_threshold' #end if $failed_out failed_reads.fastq ]]> </command> <inputs> <param argument="--in" type="data" format="fastq,fastq.gz" label="Input FASTQ file"/> <param argument="--reads_to_process" type="integer" optional="true" label="Number of reads to process" help="Limit the number of reads to process. Useful for quick QC or creating subsets."/> <param argument="--disable_quality_filtering" type="boolean" truevalue="--disable_quality_filtering" falsevalue="" checked="false" label="Disable quality filtering?" help="By default, quality filtering is enabled. Enable this option to turn it off."/> <param argument="--disable_adapter_trimming" type="boolean" truevalue="--disable_adapter_trimming" falsevalue="" checked="false" label="Disable adapter trimming?" help="By default, adapter trimming is enabled. Enable this option to turn it off."/> <param argument="--start_adapter" type="text" optional="true" label="Start adapter sequence (5')" help="Specify the adapter sequence at the 5' end of reads. Leave blank to auto-detect."/> <param argument="--end_adapter" type="text" optional="true" label="End adapter sequence (3')" help="Specify the adapter sequence at the 3' end of reads. Leave blank to auto-detect."/> <param argument="--adapter_fasta" type="data" format="fasta" optional="true" label="Adapter sequences (FASTA file)" help="Specify a FASTA file with adapter sequences to trim."/> <param argument="--distance_threshold" type="float" min="0" max="1" optional="true" label="Adapter distance threshold" help="Threshold of adapter-length. Range: 0.0–1.0"/> <param argument="--trimming_extension" type="integer" optional="true" label="Trimming extension length" help="Extend trimming beyond the adapter match to clean up the sequence more thoroughly. Default is 10"/> <param argument="--trim_front" type="integer" optional="true" label="Trim front (5') bases" help="Trim this many bases from the start (5') of each read. Default: 0"/> <param argument="--trim_tail" type="integer" optional="true" label="Trim tail (3') bases" help="Trim this many bases from the end (3') of each read. Default: 0"/> <param argument="--trim_poly_x" type="boolean" truevalue="--trim_poly_x" falsevalue="" checked="false" label="Trim polyX tails?" help="Enable to trim polyX stretches at the 3' end."/> <param argument="--poly_x_min_len" type="integer" optional="true" label="Minimum polyX length" help="Minimum length to detect polyX in the tail. Default: 10"/> <param argument="--cut_front" type="boolean" truevalue="--cut_front" falsevalue="" checked="false" label="Enable sliding-window trimming from 5' end?" help="Trim from 5' end until window mean quality is above threshold."/> <param argument="--cut_tail" type="boolean" truevalue="--cut_tail" falsevalue="" checked="false" label="Enable sliding-window trimming from 3' end?" help="Trim from 3' end until window mean quality is above threshold."/> <param argument="--cut_window_size" type="integer" optional="true" label="Sliding window size" help="Window size shared by cut_front, cut_tail, cut_sliding. Default is 4"/> <param argument="--cut_mean_quality" type="integer" optional="true" label="Mean quality threshold" help="Mean quality required for cutting. Default: 20"/> <param argument="--cut_front_window_size" type="integer" optional="true" label="Front window size" help="Override window size for cut_front only. Default: cut_window_size"/> <param argument="--cut_front_mean_quality" type="integer" optional="true" label="Front mean quality" help="Override quality threshold for cut_front only. Default: cut_mean_quality"/> <param argument="--cut_tail_window_size" type="integer" optional="true" label="Tail window size" help="Override window size for cut_tail only. Default: cut_window_size"/> <param argument="--cut_tail_mean_quality" type="integer" optional="true" label="Tail mean quality" help="Override quality threshold for cut_tail only. Default: cut_mean_quality"/> <param argument="--qualified_quality_phred" type="integer" min="0" optional="true" label="Qualified base Phred score" help="Phred quality score that counts as qualified. Default: 15"/> <param argument="--unqualified_percent_limit" type="integer" min="0" max="100" optional="true" label="Unqualified base percentage limit" help="Percent of bases allowed to be below quality threshold. Default: 40"/> <param argument="--n_base_limit" type="integer" optional="true" label="N base limit" help="Reads with more than this number of N bases are discarded. Default: 5"/> <param argument="--mean_qual" type="integer" optional="true" label="Minimum mean quality" help="Reads with mean quality below this are discarded. Default: 0"/> <param argument="--disable_length_filtering" type="boolean" truevalue="--disable_length_filtering" falsevalue="" checked="false" label="Disable length filtering?" help="Length filtering is enabled by default. Enable this to disable it."/> <param argument="--length_required" type="integer" optional="true" label="Minimum read length" help="Reads shorter than this will be discarded. Default: 15"/> <param argument="--length_limit" type="integer" optional="true" label="Maximum read length" help="Reads longer than this will be discarded. Default: 0 (no limit)"/> <param argument="--low_complexity_filter" type="boolean" truevalue="--low_complexity_filter" falsevalue="" checked="false" label="Enable low complexity filter?" help="Enable low complexity filtering."/> <param argument="--complexity_threshold" type="integer" min="0" max="100" optional="true" label="Complexity threshold (%)" help="Minimum required sequence complexity (0–100). Default: 30"/> <param argument="--failed_out" type="boolean" truevalue="--failed_out" falsevalue="" checked="false" label="Save failed reads?" help="Enable this to write failed reads to a separate FASTQ file."/> </inputs> <outputs> <data name="output" format="fastq" label="Filtered Output FASTQ"/> <data name="failed_out_reads" format="fastq" from_work_dir="failed_reads.fastq" label="Failed Reads FASTQ"> <filter>failed_out</filter> </data> <data name="json_output_default" format="json" from_work_dir="fastplong.json" label="JSON Report (default)"/> <data name="html_output_default" format="html" from_work_dir="fastplong.html" label="HTML Report (default)"/> </outputs> <tests> <test expect_num_outputs="3"> <param name="in" value="input.fastq"/> <output name="output" file="output.fastq"/> </test> <test expect_num_outputs="3"> <param name="in" value="input.fastq"/> <param name="reads_to_process" value="3"/> <output name="output" file="output_reads_to_process.fastq"/> </test> <test expect_num_outputs="4"> <param name="in" value="input.fastq"/> <param name="failed_out" value="true"/> <output name="failed_out_reads" value="output_failed_out.fastq"/> </test> </tests> <help> **Fastplong: Filter and trim long reads** This tool wraps the `fastplong` command-line tool to allow filtering and trimming of long reads in FASTQ format. **Inputs** - A FASTQ file containing reads and optional parameters to control trimming, quality filtering, adapter detection, and more. **Outputs** - A filtered FASTQ file with trimmed reads, HTML and JSON report and an optional FASTQ file of failed reads. For more information, see https://github.com/OpenGene/fastplong </help> <citations> <citation type="doi">10.1002/imt2.107</citation> <citation type="doi">10.1093/bioinformatics/bty560</citation> </citations> </tool>
