Entering edit mode
6.4 years ago
Guillermo D. Huerta
▴
10
Hi all,
I'm trying to run Trinity (2.6.6.) to analyze a metatranscriptome, but it is giving me the following errors:
Error, pairs.K25.stats is empty. Be sure to check your fastq reads and ensure that the read names are identical except for the /1 or /2 designation. at /fs/project/PAS1117/modules/trinity/2.6.6/util/insilico_read_normalization.pl line 921.
CMD finished (1209 seconds)
Error, cmd: /fs/project/PAS1117/modules/trinity/2.6.6/util/insilico_read_normalization.pl --seqType fq --JM 112G --max_cov 50 --min_cov 1 --CPU 28 --output /fs/project/PAS1117/GuiDH/Trinity_tests/trinity_out_dir/insilico_read_normalization --max_pct_stdev 10000 --left /fs/project/PAS1117/Tara_Euk/upwelling-v2/ERR1719296_1.fastq.gz --right /fs/project/PAS1117/Tara_Euk/upwelling-v2/ERR1719296_2.fastq.gz --pairs_together --PARALLEL_STATS **died with ret 512 at /fs/project/PAS1117/modules/trinity/2.6.6/Trinity line 2581.
main::process_cmd('/fs/project/PAS1117/modules/trinity/2.6.6/util/insilico_read_...') called at /fs/project/PAS1117/modules/trinity/2.6.6/Trinity line 3127
main::normalize('/fs/project/PAS1117/GuiDH/Trinity_tests/trinity_out_dir/insil...', 50, 'ARRAY(0x2735d58)', 'ARRAY(0x277bb80)') called at /fs/project/PAS1117/modules/trinity/2.6.6/Trinity line 3074
Could someone check if there is something wrong with the batch file sent? (pasted here below)
#PBS -N trinity_test3
#PBS -l walltime=40:00:00
#PBS -l nodes=1:ppn=48
#PBS -j oe
#PBS -m abe
#PBS -A PAA0034
set -x
cd $PBS_O_WORKDIR
module use /fs/project/PAS1117/modulefiles
module load samtools/1.3.1
module load bowtie2/2.2.9
module load jellyfish/2.2.9
module load salmon/0.9.1
module load trinity/2.6.6
Trinity --seqType fq --left /fs/project/PAS1117/Tara_Euk/upwelling-v2/ERR1719296_1.fastq.gz --right /fs/project/PAS1117/Tara_Euk/upwelling-v2/ERR1719296_2.fastq.gz --CPU 28 --max_memory 112G
echo $PBS_JOBID
echo $PBS-JOBNAME
Thank you!
Maybe a problem with fastq headers: Trinity v2.4.0 error ret 512 at ./Trinity line 2462. See also
How do I use reads I downloaded from SRA?
Another debbuging hint: Error, pairs.K25.stats is empty;
Hi,
thanks very much for your answer!
If you have a look to the top lines of the (right) fastq.gz file, would you say that is a matter of format?
I think the sequence header is fine, but the quality header may cause trouble. How did you download / manipulate the files? I don't know if this is the cause of the error, but the quality header line (
+ERR1719154.1.1 H10C:D1D8LACXX:2:1101:1390:2131 length=92
) is different from the sequence header line (@H10C:D1D8LACXX:2:1101:1390:2131_F/1
).