Error during Trinity running with the recent version?
0
0
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

next-gen Assembly RNA-Seq • 5.0k views
ADD COMMENT
0
Entering edit mode

Sounds like your fasta files are corrupted, check is something went wrong when you copy your files.

ADD REPLY
0
Entering edit mode

it sounds that they are right during copy. how are they corrupted? any suggested solution?

ADD REPLY
0
Entering edit mode
ADD REPLY
0
Entering edit mode

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).

ADD REPLY
0
Entering edit mode

Thank you. But I am again facing an issue. this time it is giving error:

conversion thread failed at /home/fuad/Downloads/Trinityrnaseq-v2.6.6.wExtSampleData/Trinityrnaseq-v2.6.6/util/insilico_read_normalization.pl line 333.
Error, cmd: /home/fuad/Downloads/Trinityrnaseq-v2.6.6.wExtSampleData/Trinityrnaseq-v2.6.6/util/insilico_read_normalization.pl --seqType fa --JM 4G  --max_cov 50 --min_cov 1 --CPU 4 --output /home/fuad/Downloads/Trinityoutput/insilico_read_normalization   --max_pct_stdev 10000  --SS_lib_type RF  --left /home/fuad/Downloads/catination/left.fastq --right /home/fuad/Downloads/catination/right.fastq --pairs_together --PARALLEL_STATS   died with ret 7424 at /home/fuad/Downloads/Trinityrnaseq-v2.6.6.wExtSampleData/Trinityrnaseq-v2.6.6/Trinity line 2581.
    main::process_cmd("/home/fuad/Downloads/Trinityrnaseq-v2.6.6.wExtSampleData/Trin"...) called at /home/fuad/Downloads/Trinityrnaseq-v2.6.6.wExtSampleData/Trinityrnaseq-v2.6.6/Trinity line 3127
    main::normalize("/home/fuad/Downloads/Trinityoutput/insilico_read_normalization", 50, ARRAY(0x564b84843b70), ARRAY(0x564b84843ba0)) called at /home/fuad/Downloads/Trinityrnaseq-v2.6.6.wExtSampleData/Trinityrnaseq-v2.6.6/Trinity line 3074
    main::run_normalization(50, ARRAY(0x564b84843b70), ARRAY(0x564b84843ba0)) called at /home/fuad/Downloads/Trinityrnaseq-v2.6.6.wExtSampleData/Trinityrnaseq-v2.6.6/Trinity line 1294

Can anyone please help?

ADD REPLY

Login before adding your answer.

Traffic: 2364 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6