Mercurial > repos > bgruening > nanopolish_variants
diff nanopolish_variants.xml @ 5:63af3144371a draft
"planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/nanopolish commit dff183f4eb2d3df42917ec4fed0fbdb2ea11e19a"
author | bgruening |
---|---|
date | Fri, 29 May 2020 13:29:14 -0400 |
parents | de5b3d8f5b90 |
children | bec636361cfd |
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--- a/nanopolish_variants.xml Sun Jun 23 06:04:27 2019 -0400 +++ b/nanopolish_variants.xml Fri May 29 13:29:14 2020 -0400 @@ -1,4 +1,4 @@ -<tool id="nanopolish_variants" name="Nanopolish variants" version="0.11.1"> +<tool id="nanopolish_variants" name="Nanopolish variants" version="@VERSION@+galaxy0"> <description>- Find SNPs of basecalled merged Nanopore reads and polishes the consensus sequences</description> <macros> <import>macros.xml</import> @@ -167,7 +167,18 @@ <param name="ref_file" value="draft_single_seq.fa" /> <param name="w" value="tig00000001:200000-202000" /> <output name="output_polished" file="polished.fa" /> - <output name="output_variants" file="variants.vcf"/> + <output name="output_variants"> + <assert_contents> + <has_text text="TotalReads" /> + <has_text text="AlleleCount" /> + <has_text text="SupportFraction" /> + <has_text text="200061" /> + <has_text text="200776" /> + <has_text text="201588" /> + <has_text text="tig00000001" /> + <has_n_lines n="27" /> + </assert_contents> + </output> </test> <test> <param name="input_merged" ftype="fasta" value="reads.fasta" /> @@ -177,7 +188,18 @@ <param name="ref_file" value="draft_single_seq.fa" /> <param name="w" value="tig00000001:200000-202000" /> <output name="output_polished" file="t3_polished.fa" /> - <output name="output_variants" file="t3_variants.vcf"/> + <output name="output_variants"> + <assert_contents> + <has_text text="TotalReads" /> + <has_text text="AlleleCount" /> + <has_text text="SupportFraction" /> + <has_text text="200061" /> + <has_text text="200776" /> + <has_text text="201588" /> + <has_text text="tig00000001" /> + <has_n_lines n="27" /> + </assert_contents> + </output> </test> <test> <param name="input_merged" ftype="fasta" value="reads.fasta" /> @@ -187,7 +209,18 @@ <param name="ref_file" value="draft_single_seq.fa" /> <param name="w" value="tig00000001:200000-202000" /> <output name="output_polished" file="t4_polished.fa" /> - <output name="output_variants" file="t4_variants.vcf"/> + <output name="output_variants"> + <assert_contents> + <has_text text="TotalReads" /> + <has_text text="AlleleCount" /> + <has_text text="SupportFraction" /> + <has_text text="200061" /> + <has_text text="200776" /> + <has_text text="201588" /> + <has_text text="tig00000001" /> + <has_n_lines n="27" /> + </assert_contents> + </output> </test> <test> <param name="input_merged" ftype="fasta" value="reads.fasta" /> @@ -203,7 +236,16 @@ <param name="consensus" value="false" /> <param name="min_flanking_sequence" value="10" /> <output name="output_polished" file="t2-polished.fa" /> - <output name="output_variants" file="t2-variants.vcf"/> + <output name="output_variants"> + <assert_contents> + <has_text text="TotalReads" /> + <has_text text="AlleleCount" /> + <has_text text="SupportFraction" /> + <has_text text="tig00000001" /> + <has_text text="198000-202000" /> + <has_n_lines n="15" /> + </assert_contents> + </output> </test> </tests> <help><![CDATA[