# HG changeset patch
# User iuc
# Date 1483623331 18000
# Node ID b59546214e63c52d0ea8a0103e0ddacbfe058505

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/fermikit commit 16dcfc0fb84fad80fcf18417ae46c5499c96147a

diff -r 000000000000 -r b59546214e63 all_fasta.loc.sample
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/all_fasta.loc.sample	Thu Jan 05 08:35:31 2017 -0500
@@ -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):
+#
+#<unique_build_id>	<dbkey>		<display_name>	<file_path>
+#
+#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 b59546214e63 fermi2.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/fermi2.xml	Thu Jan 05 08:35:31 2017 -0500
@@ -0,0 +1,65 @@
+<tool id="fermi2" name="fermi2" version="0.14.dev1">
+    <description>assembles Illumina reads into unitigs</description>
+    <requirements>
+        <requirement type="package" version="r193">fermi2</requirement>
+    </requirements>
+    <command detect_errors="aggressive"><![CDATA[
+        fermi2.pl unitig
+        -s$genome_size
+        -t\${GALAXY_SLOTS:-4}
+        -l$readlength
+        -p prefix "cat
+        #for fastq in $input1:
+            '$fastq'
+        #end for
+        "
+        -T $T
+        $two_pass_error
+        $E
+        > prefix.mak &&
+        make -f prefix.mak
+    ]]></command>
+    <inputs>
+        <param type="data" multiple="true" name="input1" format="fastqsanger,fastqsanger.gz"/>
+        <param argument="-l" name="readlength" type="integer" label="primary read length" value="101" min="70"/>
+        <param argument="-s" name="genome_size" type="integer" value="180000" min="1" label="approximate genome size in kilobases" help="Enter approximate genome size in kilobases. For a human genome of 3.2 gigabases enter 3200000"/>
+        <param argument="-T" type="integer" value="61" label="use INT-mer for post-trimming/filtering" min="10"/>
+        <param argument="-2" name="two_pass_error" type="boolean" checked="false" truevalue="-2" falsevalue="" label="Use 2-pass error correction"/>
+        <param argument="-E" type="boolean" checked="false" truevalue="-E" falsevalue="" label="Do not apply error correction"/>
+    </inputs>
+    <outputs>
+        <data name="unitigs" format="fastqsanger.gz" from_work_dir="prefix.mag.gz"/>
+    </outputs>
+    <tests>
+        <test>
+            <param name="input1" value="test.fastq.gz,test.fastq.gz"/>
+            <param name="readlength" value="150"/>
+            <param name="genome_size" value="1"/>
+            <output name="unitigs" file="unitigs.gz" compare="sim_size"/>
+        </test>
+    </tests>
+    <help><![CDATA[
+fermi2 can assemble reads into unitigs.
+Unitig output can be further analysed by alignment to a reference genome using bwa-mem,
+and based on the alignment variants can be called using the fermi-variants tool.
+
+::
+
+  Usage:   fermi2.pl unitig [options] <in.fq>
+
+  Options: -p STR    output prefix [fmdef]
+           -s STR    approximate genome size [100m]
+           -2        2-pass error correction
+           -l INT    primary read length [101]
+           -T INT    use INT-mer for post-trimming/filtering [61]
+           -k INT    min overlap length during unitig construction [based on -l]
+           -o INT    min overlap length during graph cleaning [based on -l]
+           -m INT    min overlap length for unambiguous merging [based on -l]
+           -t INT    number of threads [4]
+           -E        don't apply error correction
+
+    ]]></help>
+    <citations>
+        <citation type="doi">10.1093/bioinformatics/btv440</citation>
+    </citations>
+</tool>
diff -r 000000000000 -r b59546214e63 test-data/aligned_contigs.bam
Binary file test-data/aligned_contigs.bam has changed
diff -r 000000000000 -r b59546214e63 test-data/flt.vcf
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/flt.vcf	Thu Jan 05 08:35:31 2017 -0500
@@ -0,0 +1,49 @@
+##fileformat=VCFv4.1
+##source=htsbox-pileup-r327
+##reference=/tmp/tmpIcvwsb/files/000/dataset_2.dat
+##contig=<ID=11_1910000_1940000,length=30001>
+##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
+##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
+##INFO=<ID=_DP,Number=1,Type=Integer,Description="Raw read depth">
+##INFO=<ID=_DS,Number=1,Type=Integer,Description="min{alt_DP_on_forward, alt_DP_on_reverse}">
+##INFO=<ID=_AB,Number=1,Type=Integer,Description="Percentage of non-reference reads">
+##INFO=<ID=_FS,Number=1,Type=Integer,Description="Phred-scaled p-value using Fisher's exact test to detect strand bias">
+##FILTER=<ID=DPhigh,Description="High read depth: _DP>62.82">
+##FILTER=<ID=DPlow,Description="Low read depth: _DP<3">
+##FILTER=<ID=FShigh,Description="Large Fisher-Strand bias: _FS>30">
+##FILTER=<ID=ABlow,Description="Low fraction of non-reference reads: _AB<30 at SNPs or _AB<30 at INDELs">
+##FILTER=<ID=DSlow,Description="Low double-strand support at SNPs: _DS<1">
+#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	aligned_contigs_bam
+11_1910000_1940000	636	.	c	T	25	.	_DP=39;_AB=64	GT:AD	1/0:14,25
+11_1910000_1940000	708	.	t	C	40	.	_DP=40;_AB=100	GT:AD	1/1:0,40
+11_1910000_1940000	1116	.	t	C	43	.	_DP=43;_AB=100	GT:AD	1/1:0,43
+11_1910000_1940000	1891	.	t	C	44	.	_DP=44;_AB=100	GT:AD	1/1:0,44
+11_1910000_1940000	2297	.	a	G	43	.	_DP=43;_AB=100	GT:AD	1/1:0,43
+11_1910000_1940000	2727	.	a	G	42	.	_DP=42;_AB=100	GT:AD	1/1:0,42
+11_1910000_1940000	3378	.	a	G	50	.	_DP=50;_AB=100	GT:AD	1/1:0,50
+11_1910000_1940000	4140	.	c	T	21	.	_DP=36;_AB=58	GT:AD	1/0:15,21
+11_1910000_1940000	4820	.	g	A	35	.	_DP=35;_AB=100	GT:AD	1/1:0,35
+11_1910000_1940000	4860	.	t	G	36	.	_DP=36;_AB=100	GT:AD	1/1:0,36
+11_1910000_1940000	4976	.	g	A	33	.	_DP=33;_AB=100	GT:AD	1/1:0,33
+11_1910000_1940000	5455	.	a	AGT	12	.	_DP=25;_AB=48	GT:AD	0/1:13,12
+11_1910000_1940000	5559	.	g	T	39	.	_DP=39;_AB=100	GT:AD	1/1:0,39
+11_1910000_1940000	6369	.	ct	C	8	ABlow	_DP=42;_AB=19	GT:AD	0/1:34,8
+11_1910000_1940000	6654	.	g	A	43	.	_DP=43;_AB=100	GT:AD	1/1:0,43
+11_1910000_1940000	7873	.	g	A	45	.	_DP=45;_AB=100	GT:AD	1/1:0,45
+11_1910000_1940000	8084	.	t	C	54	.	_DP=54;_AB=100	GT:AD	1/1:0,54
+11_1910000_1940000	10894	.	t	G	40	.	_DP=40;_AB=100	GT:AD	1/1:0,40
+11_1910000_1940000	12259	.	a	G	35	.	_DP=35;_AB=100	GT:AD	1/1:0,35
+11_1910000_1940000	15695	.	g	A	36	.	_DP=36;_AB=100	GT:AD	1/1:0,36
+11_1910000_1940000	16353	.	ctt	C	14	.	_DP=14;_AB=100	GT:AD	1/1:0,14
+11_1910000_1940000	20714	.	c	T	24	.	_DP=42;_AB=57	GT:AD	1/0:18,24
+11_1910000_1940000	24531	.	t	G	32	.	_DP=32;_AB=100	GT:AD	1/1:0,32
+11_1910000_1940000	24546	.	gt	G	25	.	_DP=25;_AB=100	GT:AD	1/1:0,25
+11_1910000_1940000	25710	.	t	TTG	17	.	_DP=46;_AB=37	GT:AD	0/1:29,17
+11_1910000_1940000	25813	.	c	CTG,CTGTG	13	.	_DP=33;_AB=70	GT:AD	1/0:10,13,10
+11_1910000_1940000	26084	.	ctg	C,CTGTGTG	17	.	_DP=36;_AB=75	GT:AD	1/2:9,17,10
+11_1910000_1940000	26212	.	g	A	29	.	_DP=55;_AB=53	GT:AD	1/0:26,29
+11_1910000_1940000	26370	.	c	CTG,CTGTGTG	12	.	_DP=34;_AB=68	GT:AD	1/0:11,12,11
+11_1910000_1940000	26521	.	a	G	30	.	_DP=30;_AB=100	GT:AD	1/1:0,30
+11_1910000_1940000	26713	.	a	G	32	.	_DP=32;_AB=100	GT:AD	1/1:0,32
+11_1910000_1940000	27735	.	tc	T	41	.	_DP=41;_AB=100	GT:AD	1/1:0,41
+11_1910000_1940000	28524	.	c	A	18	.	_DP=38;_AB=47	GT:AD	0/1:20,18
diff -r 000000000000 -r b59546214e63 test-data/small.fa.gz
Binary file test-data/small.fa.gz has changed
diff -r 000000000000 -r b59546214e63 test-data/sv.vcf
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/sv.vcf	Thu Jan 05 08:35:31 2017 -0500
@@ -0,0 +1,16 @@
+##fileformat=VCFv4.1
+##source=htsbox-abreak-r327
+##reference=/tmp/tmpIcvwsb/files/000/dataset_2.dat
+##contig=<ID=11_1910000_1940000,length=30001>
+##ALT=<ID=DEL,Description="Deletion">
+##ALT=<ID=INS,Description="Insertion">
+##INFO=<ID=SVLEN,Number=1,Type=Integer,Description="SV length">
+##INFO=<ID=SVTYPE,Number=1,Type=String,Description="Type of structural variant">
+##INFO=<ID=END,Number=1,Type=Integer,Description="End coordinate of this variant">
+##INFO=<ID=QGAP,Number=1,Type=Integer,Description="Length of gap on the query sequence">
+##INFO=<ID=MINMAPQ,Number=1,Type=Integer,Description="Min flanking mapping quality">
+##INFO=<ID=MINSC,Number=1,Type=Integer,Description="Min flanking alignment score">
+##INFO=<ID=MINTIPQ,Number=1,Type=Integer,Description="Min quality/depth flanking the break point">
+##FILTER=<ID=LowSupp,Description="MINTIPQ < 10">
+#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO
+11_1910000_1940000	5276	.	C	<DEL>	30	.	SVTYPE=DEL;END=26956;SVLEN=21678;QGAP=3;MINMAPQ=60;MINSC=793;MINTIPQ=23
diff -r 000000000000 -r b59546214e63 test-data/test.fastq.gz
Binary file test-data/test.fastq.gz has changed
diff -r 000000000000 -r b59546214e63 test-data/unitigs.gz
Binary file test-data/unitigs.gz has changed
diff -r 000000000000 -r b59546214e63 tool_data_table_conf.xml.sample
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_data_table_conf.xml.sample	Thu Jan 05 08:35:31 2017 -0500
@@ -0,0 +1,9 @@
+<!-- Use the file tool_data_table_conf.xml.oldlocstyle if you don't want to update your loc files as changed in revision 4550:535d276c92bc-->
+<tables>
+    <!-- Locations of all fasta files under genome directory -->
+    <table name="all_fasta" comment_char="#" allow_duplicate_entries="False">
+        <columns>value, dbkey, name, path</columns>
+        <file path="tool-data/all_fasta.loc" />
+    </table>
+</tables>
+