Command line: /oak/stanford/groups/akundaje/marinovg/programs/SPAdes-3.14.0-Linux/bin/spades.py --pe1-1 /srv/scratch/marinovg/L1359-Cyanophora_paradoxa_gDNA.HT7L3DSXX_L4.read1.paired.fastq.gz --pe1-2 /srv/scratch/marinovg/L1359-Cyanophora_paradoxa_gDNA.HT7L3DSXX_L4.read2.paired.fastq.gz --s1 /srv/scratch/marinovg/L1359-Cyanophora_paradoxa_gDNA.HT7L3DSXX_L4.unpaired.fastq.gz -t 60 -o /srv/scratch/marinovg/SPAdes-3.14-L1359-Cyanophora_paradoxa_gDNA System information: SPAdes version: 3.14.0 Python version: 2.7.17 OS: Linux-4.15.0-76-generic-x86_64-with-Ubuntu-18.04-bionic Output dir: /srv/scratch/marinovg/SPAdes-3.14-L1359-Cyanophora_paradoxa_gDNA Mode: read error correction and assembling Debug mode is turned OFF Dataset parameters: Standard mode For multi-cell/isolate data we recommend to use '--isolate' option; for single-cell MDA data use '--sc'; for metagenomic data use '--meta'; for RNA-Seq use '--rna'. Reads: Library number: 1, library type: single left reads: not specified right reads: not specified interlaced reads: not specified single reads: ['/srv/scratch/marinovg/L1359-Cyanophora_paradoxa_gDNA.HT7L3DSXX_L4.unpaired.fastq.gz'] merged reads: not specified Library number: 2, library type: paired-end orientation: fr left reads: ['/srv/scratch/marinovg/L1359-Cyanophora_paradoxa_gDNA.HT7L3DSXX_L4.read1.paired.fastq.gz'] right reads: ['/srv/scratch/marinovg/L1359-Cyanophora_paradoxa_gDNA.HT7L3DSXX_L4.read2.paired.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: /srv/scratch/marinovg/SPAdes-3.14-L1359-Cyanophora_paradoxa_gDNA/tmp Threads: 60 Memory limit (in Gb): 250