# HG changeset patch
# User bgruening
# Date 1442590795 14400
# Node ID 65575e70af7e88b1564eafd4e305a747ee2bdb90
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/pileometh commit 033c712216994524fdd120b771052ac4ca9e51c0-dirty
diff -r 000000000000 -r 65575e70af7e PileOMeth.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/PileOMeth.xml Fri Sep 18 11:39:55 2015 -0400
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+ A tool for processing bisulfite sequencing alignments
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+ pileometh
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+ &1 | head -n 2 | tail -n 1]]>
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+ main_task['task'] == "extract"
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+ main_task['task'] == 'extract'
+ advanced_options['options'] == "yes"
+ advanced_options['CHG'] == "--CHG"
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+ main_task['task'] == 'extract'
+ advanced_options['options'] == "yes"
+ advanced_options['CHH'] == "--CHH"
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+ main_task['task'] == 'mbias'
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diff -r 000000000000 -r 65575e70af7e all_fasta.loc.sample
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/all_fasta.loc.sample Fri Sep 18 11:39:55 2015 -0400
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+#This file lists the locations and dbkeys of all the fasta files
+#under the "genome" directory (a directory that contains a directory
+#for each build). The script extract_fasta.py will generate the file
+#all_fasta.loc. This file has the format (white space characters are
+#TAB characters):
+#
+#
+#
+#So, all_fasta.loc could look something like this:
+#
+#apiMel3 apiMel3 Honeybee (Apis mellifera): apiMel3 /path/to/genome/apiMel3/apiMel3.fa
+#hg19canon hg19 Human (Homo sapiens): hg19 Canonical /path/to/genome/hg19/hg19canon.fa
+#hg19full hg19 Human (Homo sapiens): hg19 Full /path/to/genome/hg19/hg19full.fa
+#
+#Your all_fasta.loc file should contain an entry for each individual
+#fasta file. So there will be multiple fasta files for each build,
+#such as with hg19 above.
+#
diff -r 000000000000 -r 65575e70af7e static/images/example.svg
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/static/images/example.svg Fri Sep 18 11:39:55 2015 -0400
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diff -r 000000000000 -r 65575e70af7e test-data/cg100.fa
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/cg100.fa Fri Sep 18 11:39:55 2015 -0400
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+>chrCG
+cgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcgcA
diff -r 000000000000 -r 65575e70af7e test-data/cg_aln.bam
Binary file test-data/cg_aln.bam has changed
diff -r 000000000000 -r 65575e70af7e test-data/test_1.bedGraph
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/test_1.bedGraph Fri Sep 18 11:39:55 2015 -0400
@@ -0,0 +1,49 @@
+track type="bedGraph" description="output CpG methylation levels"
+chrCG 0 1 100 1 0
+chrCG 2 3 100 1 0
+chrCG 4 5 100 1 0
+chrCG 6 7 100 1 0
+chrCG 8 9 100 1 0
+chrCG 10 11 100 1 0
+chrCG 12 13 100 1 0
+chrCG 14 15 100 1 0
+chrCG 18 19 100 1 0
+chrCG 20 21 100 1 0
+chrCG 22 23 100 1 0
+chrCG 24 25 100 1 0
+chrCG 26 27 100 1 0
+chrCG 28 29 100 1 0
+chrCG 30 31 100 1 0
+chrCG 32 33 100 1 0
+chrCG 34 35 100 1 0
+chrCG 36 37 100 1 0
+chrCG 38 39 100 1 0
+chrCG 40 41 100 1 0
+chrCG 42 43 100 1 0
+chrCG 44 45 100 1 0
+chrCG 46 47 100 1 0
+chrCG 48 49 100 1 0
+chrCG 50 51 100 1 0
+chrCG 52 53 100 1 0
+chrCG 54 55 100 1 0
+chrCG 56 57 100 1 0
+chrCG 58 59 100 1 0
+chrCG 60 61 100 1 0
+chrCG 62 63 100 1 0
+chrCG 64 65 100 1 0
+chrCG 66 67 100 1 0
+chrCG 68 69 100 1 0
+chrCG 70 71 100 1 0
+chrCG 72 73 100 1 0
+chrCG 74 75 100 1 0
+chrCG 76 77 100 1 0
+chrCG 78 79 100 1 0
+chrCG 80 81 100 1 0
+chrCG 82 83 100 1 0
+chrCG 84 85 100 1 0
+chrCG 86 87 100 1 0
+chrCG 88 89 100 1 0
+chrCG 90 91 100 1 0
+chrCG 92 93 100 1 0
+chrCG 94 95 100 1 0
+chrCG 96 97 100 1 0
diff -r 000000000000 -r 65575e70af7e test-data/test_2_output.svg
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/test_2_output.svg Fri Sep 18 11:39:55 2015 -0400
@@ -0,0 +1,390 @@
+
diff -r 000000000000 -r 65575e70af7e tool-data/all_fasta.loc.sample
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tool-data/all_fasta.loc.sample Fri Sep 18 11:39:55 2015 -0400
@@ -0,0 +1,18 @@
+#This file lists the locations and dbkeys of all the fasta files
+#under the "genome" directory (a directory that contains a directory
+#for each build). The script extract_fasta.py will generate the file
+#all_fasta.loc. This file has the format (white space characters are
+#TAB characters):
+#
+#
+#
+#So, all_fasta.loc could look something like this:
+#
+#apiMel3 apiMel3 Honeybee (Apis mellifera): apiMel3 /path/to/genome/apiMel3/apiMel3.fa
+#hg19canon hg19 Human (Homo sapiens): hg19 Canonical /path/to/genome/hg19/hg19canon.fa
+#hg19full hg19 Human (Homo sapiens): hg19 Full /path/to/genome/hg19/hg19full.fa
+#
+#Your all_fasta.loc file should contain an entry for each individual
+#fasta file. So there will be multiple fasta files for each build,
+#such as with hg19 above.
+#
diff -r 000000000000 -r 65575e70af7e tool_data_table_conf.xml.sample
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_data_table_conf.xml.sample Fri Sep 18 11:39:55 2015 -0400
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+
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+ value, dbkey, name, path
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diff -r 000000000000 -r 65575e70af7e tool_dependencies.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_dependencies.xml Fri Sep 18 11:39:55 2015 -0400
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+ https://github.com/dpryan79/PileOMeth/archive/0.1.5.tar.gz
+ make
+ make install prefix=$INSTALL_DIR
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+ $INSTALL_DIR
+ $INSTALL_DIR
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