Entering edit mode
8.2 years ago
kingcohn
▴
30
I am using the a5 assembler to construct a de novo genome. The sample data ran without any issues but I'm getting an error with my fastq reads.
[a5] Found the following libraries:
raw1:
id=raw1
p1=/home/molecularecology/Desktop/zcpb/raw_cp3/CPBWGS_three_1.fastq.gz
p2=/home/molecularecology/Desktop/zcpb/raw_cp3/CPBWGS_three_2.fastq.gz
[a5] Found 1 libraries
[a5] Starting pipeline at step 1
[a5] Cleaning reads with SGA
[a5] Cleaning reads with SGA
cleaning each PE lib
p1 is a5CP3/CPBWGS_three_1.fastq.gz.a5unzipped
Cleaning reads
[a5] java -Xmx512m -jar '/home/molecularecology/Desktop/a5_miseq_linux_20160825/bin'/trimmomatic.jar SE -threads 4 -phred33 a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.both.fastq a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.trim.fastq ILLUMINACLIP:/home/molecularecology/Desktop/a5_miseq_linux_20160825/bin/../adapter.fasta:2:30:10 LEADING:3 TRAILING:3 SLIDINGWINDOW:4:15 MINLEN:36
TrimmomaticSE: Started with arguments: -threads 4 -phred33 a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.both.fastq a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.trim.fastq ILLUMINACLIP:/home/molecularecology/Desktop/a5_miseq_linux_20160825/bin/../adapter.fasta:2:30:10 LEADING:3 TRAILING:3 SLIDINGWINDOW:4:15 MINLEN:36
Using PrefixPair: 'TACACTCTTTCCCTACACGACGCTCTTCCGATCT' and 'GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT'
Using PrefixPair: 'TACACTCTTTCCCTACACGACGCTCTTCCGATCT' and 'TCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT'
Using PrefixPair: 'AGATGTGTATAAGAGACAG' and 'AGATGTGTATAAGAGACAG'
Using Long Clipping Sequence: 'AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTA'
Using Long Clipping Sequence: 'CTGTCTCTTATACACATCTCCGAGCCCACGAGAC'
Using Long Clipping Sequence: 'CTGTCTCTTATACACATCTGACGCTGCCGACGA'
Using Long Clipping Sequence: 'TCGTCGGCAGCGTCAGATGTGTATAAGAGACAG'
Using Long Clipping Sequence: 'GCCTCCCTCGCGCCATCAGAGATGTGTATAAGAGACAG'
Using Long Clipping Sequence: 'GCCTTGCCAGCCCGCTCAGAGATGTGTATAAGAGACAG'
Using Long Clipping Sequence: 'TACACTCTTTCCCTACACGACGCTCTTCCGATCT'
Using Long Clipping Sequence: 'AGATCGGAAGAGCGGTTCAGCAGGAATGCCGAGA'
Using Long Clipping Sequence: 'GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT'
Using Long Clipping Sequence: 'TTTTTTTTTTAATGATACGGCGACCACCGAGATCTACAC'
Using Long Clipping Sequence: 'CTGTCTCTTATACACATCTCTGATGGCGCGAGGGAGGC'
Using Long Clipping Sequence: 'CTGTCTCTTATACACATCTCTGAGCGGGCTGGCAAGGC'
Using Long Clipping Sequence: 'AGATCGGAAGAGCACACGTCTGAACTCCAGTCAC'
Using Long Clipping Sequence: 'TTTTTTTTTTCAAGCAGAAGACGGCATACGA'
Using Long Clipping Sequence: 'GTCTCGTGGGCTCGGAGATGTGTATAAGAGACAG'
Using Long Clipping Sequence: 'TCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT'
ILLUMINACLIP: Using 3 prefix pairs, 16 forward/reverse sequences, 0 forward only sequences, 0 reverse only sequences
Input Reads: 96160254 Surviving: 93109717 (96.83%) Dropped: 3050537 (3.17%)
TrimmomaticSE: Completed successfully
[a5] '/home/molecularecology/Desktop/a5_miseq_linux_20160825/bin'/sga preprocess -q 25 -f 20 -m 35 --pe-mode=0 a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.trim.fastq > a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.both.pp 2> /dev/null
[a5] sga index -d 8210180 -t 4 a5CP3.s1/a5CP3.pp.fastq > a5CP3.s1/index.out 2> a5CP3.s1/index.err
[a5] '/home/molecularecology/Desktop/a5_miseq_linux_20160825/bin'/sga correct -t 4 -p a5CP3.pp -o a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.both.pp.ec.fastq a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.both.pp > a5CP3.s1/raw1.correct.out
[timer - sga::correct] wall clock: 13901.98s CPU: 53675.25s
Running cat a5CP3.s1/CPBWGS_three_1.fastq.gz.a5unzipped.both.repair.fastq >> a5CP3.s1/a5CP3.ec.fastq
Done merging libraries
[a5_s2] Building contigs from a5CP3.ec.fastq with IDBA
[a5_s2] Building contigs from a5CP3.ec.fastq with IDBA
[a5] a5CP3.s2/a5CP3.ec.fasta has 14936675647 bytes of FastA sequence data
[a5] '/home/molecularecology/Desktop/a5_miseq_linux_20160825/bin'/idba_ud500 --num_threads 4 -r a5CP3.s2/a5CP3.ec.fasta -o a5CP3.s2/a5CP3 --mink 35 --maxk 125 --min_pairs 2
Killed
[a5] Error building contigs with IDBA
thanks for your consideration!
I have these same errors with some of my many runs, and I wonder if you or anyone else has de-bugged the source of this error, and can share it here...