Description of bug
I have a paired-end data of bacteria. After error correction using trimmomatic, I got four files: QD34_12_paired_1.fq.gz, QD34_12_paired_2.fq.gz, QD34_12_unpaired_1.fq.gz, QD34_12_unpaired_2.fq.gz. For unpaired fastq files, I don't know how to edit my YAML file. Is it right as the follow code show? Can spades recognize whether the unpaired file is forward or reverse?
YAML File
[{
"orientation": "fr",
"type": "paired-end",
"left reads": ["/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_paired_1.fq.gz"],
"right reads": ["/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_paired_2.fq.gz"]
},
{
"type": "single",
"single reads": ["/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_unpaired_1.fq.gz", "/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_unpaired_2.fq.gz"]
}]
spades.log
no
params.txt
Command line: /home/xjm/miniconda3/envs/spades/SPAdes-3.15.3-Linux/bin/spades.py --isolate --dataset /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12/QD34_12.yaml -t 28 -m 128 -o /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12
System information:
SPAdes version: 3.15.3
Python version: 3.7.8
OS: Linux-4.15.0-161-generic-x86_64-with-debian-buster-sid
Output dir: /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12
Mode: ONLY assembling (without read error correction)
Debug mode is turned OFF
Dataset parameters:
Isolate mode
Reads:
Library number: 1, library type: paired-end
orientation: fr
left reads: ['/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_paired_1.fq.gz']
right reads: ['/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_paired_2.fq.gz']
interlaced reads: not specified
single reads: not specified
merged reads: not specified
Library number: 2, library type: single
left reads: not specified
right reads: not specified
interlaced reads: not specified
single reads: ['/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_unpaired_1.fq.gz', '/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_unpaired_2.fq.gz']
merged reads: not specified
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: /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12/tmp
Threads: 28
Memory limit (in Gb): 128
SPAdes version
3.15.3
Operating System
Linux-4.15.0-161-generic-x86_64-with-debian-buster-sid
Python Version
3.7.8
Method of SPAdes installation
manual
No errors reported in spades.log
Description of bug
I have a paired-end data of bacteria. After error correction using trimmomatic, I got four files: QD34_12_paired_1.fq.gz, QD34_12_paired_2.fq.gz, QD34_12_unpaired_1.fq.gz, QD34_12_unpaired_2.fq.gz. For unpaired fastq files, I don't know how to edit my YAML file. Is it right as the follow code show? Can spades recognize whether the unpaired file is forward or reverse?
spades.log
no
params.txt
Command line: /home/xjm/miniconda3/envs/spades/SPAdes-3.15.3-Linux/bin/spades.py --isolate --dataset /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12/QD34_12.yaml -t 28 -m 128 -o /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12
System information:
SPAdes version: 3.15.3
Python version: 3.7.8
OS: Linux-4.15.0-161-generic-x86_64-with-debian-buster-sid
Output dir: /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12
Mode: ONLY assembling (without read error correction)
Debug mode is turned OFF
Dataset parameters:
Isolate mode
Reads:
Library number: 1, library type: paired-end
orientation: fr
left reads: ['/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_paired_1.fq.gz']
right reads: ['/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_paired_2.fq.gz']
interlaced reads: not specified
single reads: not specified
merged reads: not specified
Library number: 2, library type: single
left reads: not specified
right reads: not specified
interlaced reads: not specified
single reads: ['/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_unpaired_1.fq.gz', '/userData/xjm/genome_seq_Po/patch2/trimmomatic_output-1/QD34_12/QD34_12_unpaired_2.fq.gz']
merged reads: not specified
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: /userData/xjm/genome_seq_Po/patch2/spades_output/QD34_12/tmp
Threads: 28
Memory limit (in Gb): 128
SPAdes version
3.15.3
Operating System
Linux-4.15.0-161-generic-x86_64-with-debian-buster-sid
Python Version
3.7.8
Method of SPAdes installation
manual
No errors reported in spades.log