Command line: /usr/local/bin/spades.py	-o	/tmp/183/output_dir	-t	8	-m	25	--pe1-1	/tmp/183/input_1/DRR015801_1.fastq.gz	--pe1-2	/tmp/183/input_1/DRR015801_2.fastq.gz	

System information:
  SPAdes version: 3.13.1
  Python version: 3.7.3
  OS: Linux-3.10.0-1062.el7.x86_64-x86_64-with-glibc2.10

Output dir: /tmp/183/output_dir
Mode: read error correction and assembling
Debug mode is turned OFF

Dataset parameters:
  Multi-cell mode (you should set '--sc' flag if input data was obtained with MDA (single-cell) technology or --meta flag if processing metagenomic dataset)
  Reads:
    Library number: 1, library type: paired-end
      orientation: fr
      left reads: ['/tmp/183/input_1/DRR015801_1.fastq.gz']
      right reads: ['/tmp/183/input_1/DRR015801_2.fastq.gz']
      interlaced reads: not specified
      single reads: not specified
      merged reads: not specified
Read error correction parameters:
  Iterations: 1
  PHRED offset will be auto-detected
  Corrected reads will be compressed
Assembly parameters:
  k: automatic selection based on read length
  Repeat resolution is enabled
  Mismatch careful mode is turned OFF
  MismatchCorrector will be SKIPPED
  Coverage cutoff is turned OFF
Other parameters:
  Dir for temp files: /tmp/183/output_dir/tmp
  Threads: 8
  Memory limit (in Gb): 25