Mercurial > repos > florianbegusch > qiime2_suite
view qiime2/qiime_quality-filter_q-score-joined.xml @ 8:d66c7509e8f9 draft
Uploaded
author | florianbegusch |
---|---|
date | Tue, 13 Aug 2019 07:57:53 -0400 |
parents | a025a4a89e07 |
children | f190567fe3f6 |
line wrap: on
line source
<?xml version="1.0" ?> <tool id="qiime_quality-filter_q-score-joined" name="qiime quality-filter q-score-joined" version="2019.4"> <description> - Quality filter based on joined sequence quality scores.</description> <requirements> <requirement type="package" version="2019.4">qiime2</requirement> </requirements> <command><![CDATA[ qiime quality-filter q-score-joined --i-demux=$idemux #if str($pminquality): --p-min-quality=$pminquality #end if #if str($pqualitywindow): --p-quality-window=$pqualitywindow #end if #if str($pminlengthfraction): --p-min-length-fraction=$pminlengthfraction #end if #if str($pmaxambiguous): --p-max-ambiguous=$pmaxambiguous #end if --o-filtered-sequences=ofilteredsequences --o-filter-stats=ofilterstats ; cp ofilteredsequences.qza $ofilteredsequences; cp ofilterstats.qza $ofilterstats ]]></command> <inputs> <param format="qza,no_unzip.zip" label="--i-demux: ARTIFACT SampleData[JoinedSequencesWithQuality] The demultiplexed sequence data to be quality filtered. [required]" name="idemux" optional="False" type="data"/> <param label="--p-min-quality: INTEGER The minimum acceptable PHRED score. All PHRED scores less that this value are considered to be low PHRED scores. [default: 4]" name="pminquality" optional="True" type="integer" value="4"/> <param label="--p-quality-window: INTEGER The maximum number of low PHRED scores that can be observed in direct succession before truncating a sequence read. [default: 3]" name="pqualitywindow" optional="True" type="integer" value="3"/> <param label="--p-min-length-fraction: NUMBER The minimum length that a sequence read can be following truncation and still be retained. This length should be provided as a fraction of the input sequence length. [default: 0.75]" name="pminlengthfraction" optional="True" type="float" value="0.75"/> <param label="--p-max-ambiguous: INTEGER The maximum number of ambiguous (i.e., N) base calls. This is applied after trimming sequences based on `min-length-fraction`. [default: 0]" name="pmaxambiguous" optional="True" type="integer" value="0"/> </inputs> <outputs> <data format="qza" label="${tool.name} on ${on_string}: filteredsequences.qza" name="ofilteredsequences"/> <data format="qza" label="${tool.name} on ${on_string}: filterstats.qza" name="ofilterstats"/> </outputs> <help><![CDATA[ Quality filter based on joined sequence quality scores. ####################################################### This method filters joined sequence based on quality scores and the presence of ambiguous base calls. Parameters ---------- demux : SampleData[JoinedSequencesWithQuality] The demultiplexed sequence data to be quality filtered. min_quality : Int, optional The minimum acceptable PHRED score. All PHRED scores less that this value are considered to be low PHRED scores. quality_window : Int, optional The maximum number of low PHRED scores that can be observed in direct succession before truncating a sequence read. min_length_fraction : Float, optional The minimum length that a sequence read can be following truncation and still be retained. This length should be provided as a fraction of the input sequence length. max_ambiguous : Int, optional The maximum number of ambiguous (i.e., N) base calls. This is applied after trimming sequences based on `min_length_fraction`. Returns ------- filtered_sequences : SampleData[JoinedSequencesWithQuality] The resulting quality-filtered sequences. filter_stats : QualityFilterStats Summary statistics of the filtering process. ]]></help> <macros> <import>qiime_citation.xml</import> </macros> <expand macro="qiime_citation"/> </tool>