From 235fb43f046b285a3b5d8ca702b2cc8ad64dcf36 Mon Sep 17 00:00:00 2001
From: JasperBoom <jboom@infernum.nl>
Date: Tue, 15 Jun 2021 11:18:37 +0200
Subject: [PATCH] Revert changes to WDL file.

---
 bam2fastx.wdl | 29 +++++++++++++++++------------
 1 file changed, 17 insertions(+), 12 deletions(-)

diff --git a/bam2fastx.wdl b/bam2fastx.wdl
index 110441e..0bdccca 100644
--- a/bam2fastx.wdl
+++ b/bam2fastx.wdl
@@ -35,7 +35,7 @@ task Bam2Fasta {
         String dockerImage = "quay.io/biocontainers/bam2fastx:1.3.1--hf05d43a_1"
     }
 
-    command <<<
+    command {
         set -e
         mkdir -p "$(dirname ~{outputPrefix})"
 
@@ -44,13 +44,13 @@ task Bam2Fasta {
         bamFiles=""
         for bamFile in ~{sep=" " bam}
         do
-            ln -s ${bamFile} ./
-            bamFiles=${bamFiles}" ./$(basename ${bamFile})"
+            ln $bamFile .
+            bamFiles=$bamFiles" $(basename $bamFile)"
         done
 
-        for indexFile in ~{sep=" " bamIndex}
+        for index in ~{sep=" " bamIndex}
         do
-            ln -s ${indexFile} ./
+            ln $index .
         done
 
         bam2fasta \
@@ -58,8 +58,8 @@ task Bam2Fasta {
         -c ~{compressionLevel} \
         ~{true="--split-barcodes" false="" splitByBarcode} \
         ~{"--seqid-prefix " + seqIdPrefix} \
-        ${bamFiles}
-    >>>
+        $bamFiles
+    }
 
     output {
         File fastaFile = outputPrefix + ".fasta.gz"
@@ -103,7 +103,7 @@ task Bam2Fastq {
         String dockerImage = "quay.io/biocontainers/bam2fastx:1.3.1--hf05d43a_1"
     }
 
-    command <<<
+    command {
         set -e
         mkdir -p "$(dirname ~{outputPrefix})"
 
@@ -112,8 +112,13 @@ task Bam2Fastq {
         bamFiles=""
         for bamFile in ~{sep=" " bam}
         do
-            fullPathBam=$(readlink -f ${bamFile})
-            bamFiles=${bamFiles}" ${fullPathBam}"
+            ln $bamFile .
+            bamFiles=$bamFiles" $(basename $bamFile)"
+        done
+
+        for index in ~{sep=" " bamIndex}
+        do
+            ln $index .
         done
 
         bam2fastq \
@@ -121,8 +126,8 @@ task Bam2Fastq {
         -c ~{compressionLevel} \
         ~{true="--split-barcodes" false="" splitByBarcode} \
         ~{"--seqid-prefix " + seqIdPrefix} \
-        ${bamFiles}
-    >>>
+        $bamFiles
+    }
 
     output {
         File fastqFile = outputPrefix + ".fastq.gz"
-- 
GitLab