I try to run the Trinity for the RNA-Seq dataset, but I got the following error.
yuanhuang@minion12$ /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/Trinity.pl --seqType fq --JM 50G --left reads_data/SRR520139/SRR520139.sra_1.fastq --right reads_data/SRR520139/SRR520139.sra_2.fastq -CPU 6
Current settings:
core file size (blocks, -c) 0
data seg size (kbytes, -d) unlimited
scheduling priority (-e) 0
file size (blocks, -f) unlimited
pending signals (-i) 385985
max locked memory (kbytes, -l) 64
max memory size (kbytes, -m) unlimited
open files (-n) 1024
pipe size (512 bytes, -p) 8
POSIX message queues (bytes, -q) 819200
real-time priority (-r) 0
stack size (kbytes, -s) unlimited
cpu time (seconds, -t) unlimited
max user processes (-u) 1024
virtual memory (kbytes, -v) unlimited
file locks (-x) unlimited
Paired mode requires bowtie. Found bowtie at: /home/yuanhuang/bin/bowtie
Found samtools at: /home/yuanhuang/bin/samtools
-since butterfly will eventually be run, lets test for proper execution of java
#######################################
Running Java Tests
CMD: java -Xmx64m -jar /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/util/ExitTester.jar 0
CMD finished (0 seconds)
CMD: java -Xmx64m -jar /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/util/ExitTester.jar 1
-we properly captured the java failure status, as needed. Looking good.
Java tests succeeded.
###################################
-------------------------------------------
----------- Jellyfish --------------------
-- (building a k-mer catalog from reads) --
-------------------------------------------
CMD: /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/trinity-plugins/jellyfish/bin/jellyfish count -t 6 -m 25 -s 7669584440 --both-strands both.fa
terminate called after throwing an instance of 'jellyfish::file_parser::FileParserError'
what(): 'both.fa': Invalid input file. Expected fasta or fastq
Error, cmd: /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/trinity-plugins/jellyfish/bin/jellyfish count -t 6 -m 25 -s 7669584440 --both-strands both.fa died with ret 134 at /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/Trinity.pl line 1597.
What's the reason for this error? Does anybody give me the solution? Thank you so much!
yuanhuang@minion12$ /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/Trinity.pl --seqType fq --JM 50G --left reads_data/SRR520139/SRR520139.sra_1.fastq --right reads_data/SRR520139/SRR520139.sra_2.fastq -CPU 6
Current settings:
core file size (blocks, -c) 0
data seg size (kbytes, -d) unlimited
scheduling priority (-e) 0
file size (blocks, -f) unlimited
pending signals (-i) 385985
max locked memory (kbytes, -l) 64
max memory size (kbytes, -m) unlimited
open files (-n) 1024
pipe size (512 bytes, -p) 8
POSIX message queues (bytes, -q) 819200
real-time priority (-r) 0
stack size (kbytes, -s) unlimited
cpu time (seconds, -t) unlimited
max user processes (-u) 1024
virtual memory (kbytes, -v) unlimited
file locks (-x) unlimited
Paired mode requires bowtie. Found bowtie at: /home/yuanhuang/bin/bowtie
Found samtools at: /home/yuanhuang/bin/samtools
-since butterfly will eventually be run, lets test for proper execution of java
#######################################
Running Java Tests
CMD: java -Xmx64m -jar /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/util/ExitTester.jar 0
CMD finished (0 seconds)
CMD: java -Xmx64m -jar /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/util/ExitTester.jar 1
-we properly captured the java failure status, as needed. Looking good.
Java tests succeeded.
###################################
-------------------------------------------
----------- Jellyfish --------------------
-- (building a k-mer catalog from reads) --
-------------------------------------------
CMD: /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/trinity-plugins/jellyfish/bin/jellyfish count -t 6 -m 25 -s 7669584440 --both-strands both.fa
terminate called after throwing an instance of 'jellyfish::file_parser::FileParserError'
what(): 'both.fa': Invalid input file. Expected fasta or fastq
Error, cmd: /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/trinity-plugins/jellyfish/bin/jellyfish count -t 6 -m 25 -s 7669584440 --both-strands both.fa died with ret 134 at /home/yuanhuang/bin/trinityrnaseq_r2013_08_14/Trinity.pl line 1597.
What's the reason for this error? Does anybody give me the solution? Thank you so much!
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