| Previous changeset 3:bc79b5b0fe04 (2019-06-19) Next changeset 5:63af3144371a (2020-05-29) |
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Commit message:
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/nanopolish commit 25c22b467760e4784e199125292927bd2274a189-dirty |
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modified:
nanopolish_variants.xml |
| b |
| diff -r bc79b5b0fe04 -r de5b3d8f5b90 nanopolish_variants.xml --- a/nanopolish_variants.xml Wed Jun 19 03:46:05 2019 -0400 +++ b/nanopolish_variants.xml Sun Jun 23 06:04:27 2019 -0400 |
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| @@ -1,4 +1,4 @@ -<tool id="nanopolish_variants" name="Nanopolish variants" version="0.1.0"> +<tool id="nanopolish_variants" name="Nanopolish variants" version="0.11.1"> <description>- Find SNPs of basecalled merged Nanopore reads and polishes the consensus sequences</description> <macros> <import>macros.xml</import> @@ -98,7 +98,7 @@ <inputs> <!-- index inputs --> <param type="data" name="input_merged" format="fasta,fastq" label="Basecalled merged reads.fa"/> - <param type="data" name="input_reads_raw" format="h5,fast5.tar.gz,fast5.tar.bz2,fast5.tar" label="Flat archive file of raw fast5 files"/> + <param type="data" name="input_reads_raw" format="fast5.tar.gz,fast5.tar.bz2,fast5.tar" label="Flat archive file of raw fast5 files"/> <!-- variants consensus inputs --> <param type="data" argument="-b" format="bam" label="Reads aligned to the reference genome" /> |