# HG changeset patch
# User kpbioteam
# Date 1550852255 18000
# Node ID b0b6949347511e8f4176b6ce9b64c2aaef659eb1
# Parent  e3932f28bf3680ab9a743b9a09eb5843866dfdb0
Uploaded

diff -r e3932f28bf36 -r b0b694934751 minfi_dmp.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/minfi_dmp.xml	Fri Feb 22 11:17:35 2019 -0500
@@ -0,0 +1,97 @@
+<tool id="minfi_dmp" name="Minfi DMP" version="@MINFI_VERSION@">
+    <description>to find differentially methylated positions</description>
+    <macros>
+        <import>macros.xml</import>
+    </macros>
+    <expand macro="requirements" />
+    <command detect_errors="exit_code"><![CDATA[
+        Rscript '$minfi_dmp_script'
+    ]]></command>
+    <configfiles>
+        <configfile name="minfi_dmp_script"><![CDATA[
+require("minfi", quietly = TRUE)
+
+set <- get(load('$grset'))
+
+genomeranges <- as.data.frame(ranges(set))
+
+beta <- getBeta(set)
+
+pheno <- read.table('$phenotype_table',skip=1)
+
+type <- '$phenotype'
+
+qCutoff <- as.numeric('$q_cutoff')
+
+shrinkVar <- '$variance_shrinkage'
+
+tab <- read.table('$ucsc_genome')
+
+tab <- tab[,-(11:14),drop=FALSE] 
+
+colnames(tab) <- c("seqname","source","feature","start","end","score","strand", "frame","attributes", "names")
+
+tab[,"source"] <- NULL
+
+tab[,"frame"] <- NULL
+
+tab[,"attributes"] <- NULL
+
+dmp <- dmpFinder(beta, pheno[,"V2"], type = type, qCutoff = qCutoff, shrinkVar = shrinkVar)
+
+dmp[,"names"] <- rownames(dmp)
+
+data <- merge(dmp, tab, by="names",sort = TRUE)
+
+data <- data[c("seqname","start","end","names","score","strand", "feature","intercept", "f", "pval","qval")]
+
+write.table(data, file= '$dmp', quote = FALSE,col.names = FALSE, row.names = FALSE, sep = "\t")
+    ]]>
+        </configfile>
+    </configfiles> 
+    <inputs>
+        <param type="data" name="grset" format="rdata" label="Input Set" help="MethylSet, RatioSet or GenomicRatioSet" />
+        <param type="data" name="phenotype_table" format="tabular" label="Phenotype Table"/>
+        <param name="phenotype" type="select" label="Phenotype Type">
+            <option value="categorical">categorical</option>
+            <option value="continuous">continuous</option>
+        </param> 
+        <param name="q_cutoff" type="integer" value="1" label="qCutoff Size" help="DMPs with an FDR q-value greater than this will not be returned."/>
+        <param name="variance_shrinkage" type="boolean" truevalue="TRUE" falsevalue="FALSE" label="Variance Shrinkage"
+            help="Enable variance shrinkage is recommended when sample sizes are small"/>
+        <param type="data" name="ucsc_genome" format="gtf" label="Genome Table" help="UCSC genome data Methyl450"/>
+    </inputs>
+    <outputs>
+        <data name="dmp" format="interval" label="Differentially Methylated Positions"/>
+    </outputs>
+    <tests>
+        <test>
+            <param name="grset" value="GRSet_without_SNPs.rdata"/>
+            <param name="phenotype_table" value="phenotypeTable.txt"/>
+            <param name="phenotype" value="categorical"/>
+            <param name="q_cutoff" value="1"/>
+            <param name="variance_shrinkage" value="FALSE"/>
+            <param name="ucsc_genome" value="ucsc.gtf"/>
+            <output name="dmp" file="Differentially_Methylated_Positions.interval"/>
+        </test>
+    </tests>
+    <help><![CDATA[
+This tool creates differentially methylated positions (DMPs) with respect to a phenotype covariate. The phenotype may be categorical (e.g. cancer vs. normal) or continuous (e.g. blood pressure). 
+
+The output is an interval file with the following columns:
+
+    - seqnames
+    - start
+    - end
+    - cpg
+    - names
+    - score
+    - strand
+    - feature
+    - intercept
+    - f pval
+    - qval
+
+ ]]></help>
+    <expand macro="citations" />
+</tool>