Entering edit mode
9.6 years ago
seta
★
1.9k
Hi all,
I'm using last version of Trinity (20140717) to make de novo transcriptome assembly of large fastq.gz files, but the program immediately give me the following error
fastool: parsing error, truncated sequence and/or quality detected!
Thread 1 terminated abnormally: Error, cmd: /home/jafarinezhad/software/trinityrnaseq_r20140717/util/..//trinity-plugins/fastool/fastool --illumina-trinity --to-fasta /home/jafarinezhad/software/trinityrnaseq_r20140717/newreads1.fq.gz >> left.fa died with ret 256 at /home/jafarinezhad/software/trinityrnaseq_r20140717/util/insilico_read_normalization.pl line 719.
CMD finished (0 seconds)
Error, conversion thread failed at /home/jafarinezhad/software/trinityrnaseq_r20140717/util/insilico_read_normalization.pl line 329.
Error, cmd: /home/jafarinezhad/software/trinityrnaseq_r20140717/util/insilico_read_normalization.pl --seqType fq --JM 150G --max_cov 50 --CPU 6 --output /home/jafarinezhad/software/trinityrnaseq_r20140717/trinity_out_dir/insilico_read_normalization --SS_lib_type FR --left /home/jafarinezhad/software/trinityrnaseq_r20140717/newreads1.fq.gz --right /home/jafarinezhad/software/trinityrnaseq_r20140717/newreads2.fq.gz --pairs_together --PARALLEL_STATS died with ret 7424 at ./Trinity line 1990.
Is anybody faced with this error, how should solve it? Thanks
Sounds like your fasta files are corrupted, check is something went wrong when you copy your files.
it sounds that they are right during copy. how are they corrupted? any suggested solution?
Fastq Quality Read And Score Length Check
Even when you didn't get any error message, sometimes bytes just flip and corrupt a compressed file (disk I/O have some errors that cannot be predicted).
Thank you. But I am again facing an issue. this time it is giving error:
Can anyone please help?