# HG changeset patch # User iuc # Date 1623674890 0 # Node ID a92a632c4d9bd87c702bc9d38363b475600e80e5 # Parent b89b0765695d3344e26b8beb3f499c11e7ed6264 "planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/metaphlan/ commit f1c6f4fe1e572ace84cf9106bc253603f55aac55" diff -r b89b0765695d -r a92a632c4d9b formatoutput.py --- a/formatoutput.py Mon May 17 20:10:24 2021 +0000 +++ b/formatoutput.py Mon Jun 14 12:48:10 2021 +0000 @@ -57,7 +57,9 @@ # skip headers if line.startswith("#"): continue - + # skip UNKNOWN lines in Predicted taxon relative abundances + if "UNKNOWN" in line: + continue # spit lines split_line = line[:-1].split('\t') taxo_n = split_line[0].split('|') diff -r b89b0765695d -r a92a632c4d9b macros.xml --- a/macros.xml Mon May 17 20:10:24 2021 +0000 +++ b/macros.xml Mon Jun 14 12:48:10 2021 +0000 @@ -1,6 +1,6 @@ - 3.0.8 + 3.0.9 0 20.01 @@ -21,7 +21,7 @@ - 1101/2020.11.19.388223 + 10.7554/eLife.65088 diff -r b89b0765695d -r a92a632c4d9b metaphlan.xml --- a/metaphlan.xml Mon May 17 20:10:24 2021 +0000 +++ b/metaphlan.xml Mon Jun 14 12:48:10 2021 +0000 @@ -195,8 +195,7 @@ --metaphlan_output '$output_file' --outdir 'split_levels' $out.legacy_output -&& -ls split_levels + #end if #if $out.krona_output @@ -211,26 +210,26 @@
- + - + - + - + - + - - + + @@ -245,10 +244,10 @@
- + - @@ -273,12 +272,12 @@
- - + + - + @@ -296,8 +295,8 @@ - + @@ -369,6 +368,152 @@ + + + +
+ + +
+
+ + + + + +
+
+ + + + + + + + + + + + + +
+
+ + + + + + + +
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ + + + + @@ -916,13 +1061,13 @@ - species-level resolution for bacteria, archaea, eukaryotes and viruses; - strain identification and tracking - orders of magnitude speedups compared to existing methods. -- metagenomic strain-level population genomics +- microbiota strain-level population genomics MetaPhlAn clade-abundance estimation ------------------------------------ The basic usage of MetaPhlAn consists in the identification of the clades (from phyla to species and -strains in particular cases) present in the metagenome obtained from a microbiome sample and their +strains in particular cases) present in the microbiota obtained from a microbiome sample and their relative abundance. Marker level analysis @@ -944,7 +1089,7 @@ - one or several sequence files in Fasta, FastQ (compressed or not) - a BowTie2 produced SAM file -- an intermediary mapping file of the metagenome generated by a previous MetaPhlAn run +- an intermediary mapping file of the microbiota generated by a previous MetaPhlAn run It also need the reference database, which can be locally installed or customized using the dedicated tools. @@ -965,4 +1110,4 @@ ]]> - + \ No newline at end of file diff -r b89b0765695d -r a92a632c4d9b test-data/no_taxon_input.fasta --- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/test-data/no_taxon_input.fasta Mon Jun 14 12:48:10 2021 +0000 @@ -0,0 +1,4 @@ +> seq1 +ATTAGGGATTTTAGGGGGGGAGATTTAGAGAGAGAGAGAGAGAAGAAGAGAAGAAGAAGAAGAAAAAGGGGGAAGAGAGA +> seq2 +ATTAGGGATTTTAGGGGGGGAGATTTAGAGAGAGAGAGAGAGAAGAAGAGAAGAAGAAGAAGAAAAAGGGGGAAGAGAGA