diff check_sam_present.xml @ 0:e979cb57a5d5 draft default tip

"planemo upload for repository https://github.com/McIntyre-Lab/BayesASE/tree/main/galaxy commit 9b70598ef46a73632d9e0fa0c6ce6776fb5e9d6a"
author malex
date Thu, 14 Jan 2021 21:51:36 +0000
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--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/check_sam_present.xml	Thu Jan 14 21:51:36 2021 +0000
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+<tool id="check_sam_present" name="Verify that two input SAM files are present" version="21.1.13">
+    <description>verify 2 SAM files are present for every 1 FASTQ file.</description>
+    <macros>
+        <import>macros.xml</import>
+    </macros>
+    <expand macro="requirements"/>
+    <command><![CDATA[
+    check_sam_present.py
+    --fq=$fq.element_identifier
+    --alnType=$alnType
+    --sam1=$sam1
+    --sam2=$sam2
+    --out=$out
+]]></command>
+    <inputs>
+        <param name="alnType" size="30" type="select" value="" display="radio" label="Align Type" help="For BayesASE without modification, select Single End. Select whether SAM files were created from single end or paired end alignments.">
+            <option value="SE" selected="true">Single End</option>
+            <option value="PE" selected="true">Paired End</option>
+        </param>
+        <param name="sam1" type="data" format="sam" label="Unique SAM for G1" help="Select the SAM file [from BWASplitSAM] for updated genome1 containing only uniquely mapped reads."/>
+        <param name="sam2" type="data" format="sam" label="Unique SAM for G2" help="Select the SAM file [from BWASplitSAM] for updated genome2 containing uniquely mapped reads. "/>
+        <param name="fq" type="data" format="fastq" label="FastQ file" help="Select the FastQ file used to generate the SAM files." />
+    </inputs>
+    <outputs>
+        <data name="out" format="tabular" label="${tool.name} on ${on_string}:Check for 2 SAM Files"/>
+    </outputs>
+    <tests>
+        <test>
+            <param name="fq" ftype="data" value="align_and_counts_test_data/W55_M_1_1.fastq"/>
+            <param name="alnType" ftype="select" value="SE"/>
+            <param name="sam1" ftype="data"      value="align_and_counts_test_data/W1118_G1_unique_sam_for_BASE.sam"/>
+            <param name="sam2" ftype="data"      value="align_and_counts_test_data/W55_G2_unique_sam_for_BASE.sam"/>
+            <output name="out"       file="align_and_counts_test_data/check_SAM_present_BASE_test_data.tabular" />
+        </test>
+    </tests>
+    <help><![CDATA[
+
+**Tool Description**
+
+This tool checks to make sure that **2 SAM files** were generated from **1 FASTQ file** (one for each updated parental genome).
+
+**NOTE:**  If you are running the BayesASE Align and Count workflow without modification, all reads are aligned as Single End - select Single End
+
+
+**Inputs**
+
+**FASTQ File [Required]**
+
+The FASTQ file used to generate the SAM files
+
+**Alignment Type [Required]**
+
+Select from drop-down menu how the FASTQ file was aligned - this will be SE if running the BayesASE workflow.
+
+**2 Unique SAM files [Required]**
+-Two SAM files containing uniquely mapping reads. These can be created by the *BWASplitSAM Tool*.
+
+(1) The unique SAM file generated by alignments to updated genome1
+(2) The unique SAM file generated by alignments to updated genome2
+
+
+**Output**
+
+	(1) A single TSV file containing information on whether 2 SAM files are present per FASTQ file or not.
+
+Example of output:
+
+    +-------------------+--------------------------+
+    |   fqName          |   message                |
+    +===================+==========================+
+    |dataset_1795.dat   | Have 2 SAM files - good! |
+    +-------------------+--------------------------+
+
+    ]]></help>
+    <citations>
+            <citation type="bibtex">@ARTICLE{Miller20BASE,
+            author = {Brecca Miller, Alison M. Morse, Elyse Borgert, Zihao Liu, Kelsey Sinclair, Gavin Gamble, Fei Zou, Jeremy Newman, Luis Leon Novello, Fabio Marroni, Lauren M. McIntyre},
+            title = {Testcrosses are an efficient strategy for identifying cis regulatory variation: Bayesian analysis of allele imbalance among conditions (BASE)},
+            journal = {????},
+            year = {submitted for publication}
+            }</citation>
+        </citations>
+</tool>