Hello,everyone.
I am using Trinity(v2012-06-08) for de novo assembly, and the size of paired end reads files is 45.1G (2*22.6G), I used the followed command to do this:
perl Trinity.pl --seqType fq --JM 80G --left mixed_1.fq --right mixed_2.fq --min_contig_length 200 --CPU 10
but this message was gived back to me:
Error, the Chrysalis process failed:
Error, cmd: /home/mbl/softwares/trinityrnaseq_r2012-06-08/Chrysalis/Chrysalis -i both.fa -iworm /home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir/inchworm.K25.L25.DS.fa -o chrysalis -cpu 10 -min_glue 2 -min_iso_ratio 0.05 -glue_factor 0.05 -weldmer_size 48 -min 200 -dist 500 -max_reads 20000000 -max_mem_reads 1000000 -paired -butterfly /home/mbl/softwares/trinityrnaseq_r2012-06-08/Butterfly/Butterfly.jar 2>&1 died with ret 65280 at Trinity.pl line 1128.
at Trinity.pl line 808
main::run_chrysalis('/home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir...', 'both.fa', 200, 500, undef) called at Trinity.pl line 681
what happened? Who can help me?
I am using Trinity(v2012-06-08) for de novo assembly, and the size of paired end reads files is 45.1G (2*22.6G), I used the followed command to do this:
perl Trinity.pl --seqType fq --JM 80G --left mixed_1.fq --right mixed_2.fq --min_contig_length 200 --CPU 10
but this message was gived back to me:
Error, the Chrysalis process failed:
Error, cmd: /home/mbl/softwares/trinityrnaseq_r2012-06-08/Chrysalis/Chrysalis -i both.fa -iworm /home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir/inchworm.K25.L25.DS.fa -o chrysalis -cpu 10 -min_glue 2 -min_iso_ratio 0.05 -glue_factor 0.05 -weldmer_size 48 -min 200 -dist 500 -max_reads 20000000 -max_mem_reads 1000000 -paired -butterfly /home/mbl/softwares/trinityrnaseq_r2012-06-08/Butterfly/Butterfly.jar 2>&1 died with ret 65280 at Trinity.pl line 1128.
at Trinity.pl line 808
main::run_chrysalis('/home/mbl/softwares/trinityrnaseq_r2012-06-08/trinity_out_dir...', 'both.fa', 200, 500, undef) called at Trinity.pl line 681
what happened? Who can help me?
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