--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/qiime2__deblur__denoise_16S.xml	Mon Aug 29 19:25:20 2022 +0000
@@ -0,0 +1,87 @@
+<?xml version='1.0' encoding='utf-8'?>
+<!--
+Copyright (c) 2022, QIIME 2 development team.
+
+Distributed under the terms of the Modified BSD License. (SPDX: BSD-3-Clause)
+-->
+<!--
+This tool was automatically generated by:
+    q2galaxy (version: 2022.8.1)
+for:
+    qiime2 (version: 2022.8.1)
+-->
+<tool name="qiime2 deblur denoise-16S" id="qiime2__deblur__denoise_16S" version="2022.8.0+q2galaxy.2022.8.1.2" profile="22.05" license="BSD-3-Clause">
+    <description>Deblur sequences using a 16S positive filter.</description>
+    <requirements>
+        <container type="docker">quay.io/qiime2/core:2022.8</container>
+    </requirements>
+    <version_command>q2galaxy version deblur</version_command>
+    <command detect_errors="aggressive">q2galaxy run deblur denoise_16S '$inputs'</command>
+    <configfiles>
+        <inputs name="inputs" data_style="paths"/>
+    </configfiles>
+    <inputs>
+        <param name="demultiplexed_seqs" type="data" format="qza" label="demultiplexed_seqs: SampleData[SequencesWithQuality | PairedEndSequencesWithQuality | JoinedSequencesWithQuality]" help="[required]  The demultiplexed sequences to be denoised.">
+            <options options_filter_attribute="metadata.semantic_type">
+                <filter type="add_value" value="SampleData[PairedEndSequencesWithQuality]"/>
+                <filter type="add_value" value="SampleData[JoinedSequencesWithQuality]"/>
+                <filter type="add_value" value="SampleData[SequencesWithQuality]"/>
+            </options>
+            <validator type="expression" message="Incompatible type">hasattr(value.metadata, "semantic_type") and value.metadata.semantic_type in ['SampleData[JoinedSequencesWithQuality]', 'SampleData[PairedEndSequencesWithQuality]', 'SampleData[SequencesWithQuality]']</validator>
+        </param>
+        <param name="trim_length" type="integer" value="" label="trim_length: Int" help="[required]  Sequence trim length, specify -1 to disable trimming."/>
+        <section name="__q2galaxy__GUI__section__extra_opts__" title="Click here for additional options">
+            <param name="left_trim_len" type="integer" min="0" value="0" label="left_trim_len: Int % Range(0, None)" help="[default: 0]  Sequence trimming from the 5' end. A value of 0 will disable this trim."/>
+            <param name="sample_stats" type="boolean" truevalue="__q2galaxy__::literal::True" falsevalue="__q2galaxy__::literal::False" label="sample_stats: Bool" help="[default: No]  If true, gather stats per sample."/>
+            <param name="mean_error" type="float" value="0.005" label="mean_error: Float" help="[default: 0.005]  The mean per nucleotide error, used for original sequence estimate."/>
+            <param name="indel_prob" type="float" value="0.01" label="indel_prob: Float" help="[default: 0.01]  Insertion/deletion (indel) probability (same for N indels)."/>
+            <param name="indel_max" type="integer" value="3" label="indel_max: Int" help="[default: 3]  Maximum number of insertion/deletions."/>
+            <param name="min_reads" type="integer" value="10" label="min_reads: Int" help="[default: 10]  Retain only features appearing at least min_reads times across all samples in the resulting feature table."/>
+            <param name="min_size" type="integer" value="2" label="min_size: Int" help="[default: 2]  In each sample, discard all features with an abundance less than min_size."/>
+            <param name="jobs_to_start" type="integer" value="1" label="jobs_to_start: Int" help="[default: 1]  Number of jobs to start (if to run in parallel)."/>
+            <param name="hashed_feature_ids" type="boolean" truevalue="__q2galaxy__::literal::True" falsevalue="__q2galaxy__::literal::False" checked="true" label="hashed_feature_ids: Bool" help="[default: Yes]  If true, hash the feature IDs."/>
+        </section>
+    </inputs>
+    <outputs>
+        <data name="table" format="qza" label="${tool.name} on ${on_string}: table.qza" from_work_dir="table.qza"/>
+        <data name="representative_sequences" format="qza" label="${tool.name} on ${on_string}: representative_sequences.qza" from_work_dir="representative_sequences.qza"/>
+        <data name="stats" format="qza" label="${tool.name} on ${on_string}: stats.qza" from_work_dir="stats.qza"/>
+    </outputs>
+    <tests/>
+    <help>
+QIIME 2: deblur denoise-16S
+===========================
+Deblur sequences using a 16S positive filter.
+
+
+Outputs:
+--------
+:table.qza: The resulting denoised feature table.
+:representative_sequences.qza: The resulting feature sequences.
+:stats.qza: Per-sample stats if requested.
+
+|  
+
+Description:
+------------
+Perform sequence quality control for Illumina data using the Deblur workflow with a 16S reference as a positive filter. Only forward reads are supported at this time. The specific reference used is the 88% OTUs from Greengenes 13_8. This mode of operation should only be used when data were generated from a 16S amplicon protocol on an Illumina platform. The reference is only used to assess whether each sequence is likely to be 16S by a local alignment using SortMeRNA with a permissive e-value; the reference is not used to characterize the sequences.
+
+
+|  
+
+</help>
+    <citations>
+        <citation type="bibtex">@article{cite1,
+ author = {Amir, Amnon and McDonald, Daniel and Navas-Molina, Jose A and Kopylova, Evguenia and Morton, James T and Xu, Zhenjiang Zech and Kightley, Eric P and Thompson, Luke R and Hyde, Embriette R and Gonzalez, Antonio and Knight, Rob},
+ journal = {MSystems},
+ number = {2},
+ pages = {e00191--16},
+ publisher = {Am Soc Microbiol},
+ title = {Deblur rapidly resolves single-nucleotide community sequence patterns},
+ volume = {2},
+ year = {2017}
+}
+</citation>
+        <citation type="doi">10.1038/s41587-019-0209-9</citation>
+    </citations>
+</tool>