System information:
SPAdes version: 3.14.0
Python version: 3.8.1
OS: Linux-4.4.0-166-generic-x86_64-with-glibc2.10
Output dir: /home/u4244/data/tb/0-ref/2-assembly/spades
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: paired-end
orientation: fr
left reads: ['/home/u4244/data/tb/0-ref/1-mapping/bwa_R1.fastq']
right reads: ['/home/u4244/data/tb/0-ref/1-mapping/bwa_R2.fastq']
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: [21, 33, 55, 77]
Repeat resolution is enabled
Mismatch careful mode is turned ON
MismatchCorrector will be used
Coverage cutoff is turned OFF
Other parameters:
Dir for temp files: /home/u4244/data/tb/0-ref/2-assembly/spades/tmp
Threads: 16
Memory limit (in Gb): 94
======= SPAdes pipeline started. Log can be found here: /home/u4244/data/tb/0-ref/2-assembly/spades/spades.log
max() arg is an empty sequence
Traceback (most recent call last):
File "/home/u4244/anaconda3/envs/spades/bin/spades.py", line 589, in main
build_pipeline(pipeline, cfg, output_files, tmp_configs_dir, dataset_data, log,
File "/home/u4244/anaconda3/envs/spades/bin/spades.py", line 529, in build_pipeline
spades_stage.add_to_pipeline(pipeline, get_stage, cfg, output_files, tmp_configs_dir, dataset_data, log, bin_home,
File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/stages/spades_stage.py", line 377, in add_to_pipeline
pipeline.add(SpadesStage(cfg, get_stage, "as", output_files, tmp_configs_dir,
File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/stages/spades_stage.py", line 286, in init
generateK(self.cfg, self.log, self.dataset_data)
File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/stages/spades_stage.py", line 121, in generateK
RL = support.get_primary_max_reads_length(dataset_data, log, ["merged reads"],
File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/support.py", line 620, in get_primary_max_reads_length
max_reads_lenghts = [get_max_reads_length(reads_file, log, num_checked) for reads_file in
File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/support.py", line 620, in
max_reads_lenghts = [get_max_reads_length(reads_file, log, num_checked) for reads_file in
File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/support.py", line 651, in get_max_reads_length
max_reads_length = max(
ValueError: max() arg is an empty sequence
Command line: /home/u4244/anaconda3/envs/spades/bin/spades.py -k 21,33,55,77 --careful -1 /home/u4244/data/tb/0-ref/1-mapping/bwa_R1.fastq -2 /home/u4244/data/tb/0-ref/1-mapping/bwa_R2.fastq -o /home/u4244/data/tb/0-ref/2-assembly/spades
System information: SPAdes version: 3.14.0 Python version: 3.8.1 OS: Linux-4.4.0-166-generic-x86_64-with-glibc2.10
Output dir: /home/u4244/data/tb/0-ref/2-assembly/spades 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: paired-end orientation: fr left reads: ['/home/u4244/data/tb/0-ref/1-mapping/bwa_R1.fastq'] right reads: ['/home/u4244/data/tb/0-ref/1-mapping/bwa_R2.fastq'] 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: [21, 33, 55, 77] Repeat resolution is enabled Mismatch careful mode is turned ON MismatchCorrector will be used Coverage cutoff is turned OFF Other parameters: Dir for temp files: /home/u4244/data/tb/0-ref/2-assembly/spades/tmp Threads: 16 Memory limit (in Gb): 94
======= SPAdes pipeline started. Log can be found here: /home/u4244/data/tb/0-ref/2-assembly/spades/spades.log
max() arg is an empty sequence Traceback (most recent call last): File "/home/u4244/anaconda3/envs/spades/bin/spades.py", line 589, in main build_pipeline(pipeline, cfg, output_files, tmp_configs_dir, dataset_data, log, File "/home/u4244/anaconda3/envs/spades/bin/spades.py", line 529, in build_pipeline spades_stage.add_to_pipeline(pipeline, get_stage, cfg, output_files, tmp_configs_dir, dataset_data, log, bin_home, File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/stages/spades_stage.py", line 377, in add_to_pipeline pipeline.add(SpadesStage(cfg, get_stage, "as", output_files, tmp_configs_dir, File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/stages/spades_stage.py", line 286, in init generateK(self.cfg, self.log, self.dataset_data) File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/stages/spades_stage.py", line 121, in generateK RL = support.get_primary_max_reads_length(dataset_data, log, ["merged reads"], File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/support.py", line 620, in get_primary_max_reads_length max_reads_lenghts = [get_max_reads_length(reads_file, log, num_checked) for reads_file in File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/support.py", line 620, in
max_reads_lenghts = [get_max_reads_length(reads_file, log, num_checked) for reads_file in
File "/home/u4244/anaconda3/envs/spades/share/spades/spades_pipeline/support.py", line 651, in get_max_reads_length
max_reads_length = max(
ValueError: max() arg is an empty sequence
== Error == exception caught: <class 'ValueError'>