the filename templates were moved from condorfastq to fastqname a while ago
authorDiane Trout <diane@caltech.edu>
Mon, 12 May 2014 23:14:18 +0000 (16:14 -0700)
committerDiane Trout <diane@ghic.org>
Tue, 10 Jun 2014 23:29:41 +0000 (16:29 -0700)
htsworkflow/submission/condorfastq.py

index ffbd8e0704356f4798d2dfb3790734bdcc782c9c..b6c22348f581f5148eeaa33cacfafe65f6ebc963 100644 (file)
@@ -220,8 +220,6 @@ WHERE {
         Also update model with link between illumina result files
         and our target fastq file.
         """
-        fastq_paired_template = '%(lib_id)s_%(flowcell)s_c%(cycle)s_l%(lane)s_r%(read)s.fastq'
-        fastq_single_template = '%(lib_id)s_%(flowcell)s_c%(cycle)s_l%(lane)s.fastq'
         # find what targets we're missing
         needed_targets = {}
         for seq in raw_files: