important fastp fix

src/batch_processor.py

@@ -15,7 +15,7 @@ LOGTYPE_DEBUG = 'DEBUG'
 def fastp(accession,folder,sdb,extra_args=""):
     # Separate fastq files into paired- and single-end reads
     #based on https://github.com/hawkjo/sequencetools/blob/master/clean_fastqs_in_subdirs.py
-    fastq_files = glob.glob(folder+"*.fastq")
+    fastq_files = glob.glob(folder+"/"+accession+"*.fastq")
     pe_fastq_files = []
     se_fastq_files = []
     for fname in fastq_files: