Entering edit mode
10.3 years ago
subodh
•
0
Hi everyone,
I have a problem in running tophat 2.0.11 with a 50 bp paired end illumina RNA reads.
I have used following command:
./tophat2 \
--read-gap-length 2 \
-r 50 \
--mate-std-dev 20 \
-o /home/sandor/Desktop/HD/NGS_analysis/tophat-2.0.11.Linux_x86_64/tophat_out \
-m 0 \
-i 70 \
-I 500000 \
--max-insertion-length 3 \
--max-deletion-length 3 \
-p 4 \
--report-secondary-alignments \
--no-coverage-search \
--segment-length 25 \
/home/sandor/Desktop/HD/NGS_analysis/tophat-2.0.11.Linux_x86_64/hg19_indexes/hg19 \
A4EP_GCCAAT_L004_R1_001.fastq_filtered \
A4EP_GCCAAT_L004_R2_001.fastq_filtered
The output was as follows:
[2014-07-28 10:47:10] Beginning TopHat run (v2.0.11)
-----------------------------------------------
[2014-07-28 10:47:10] Checking for Bowtie
Bowtie version: 2.2.2.0
[2014-07-28 10:47:10] Checking for Samtools
Samtools version: 0.1.18.0
[2014-07-28 10:47:10] Checking for Bowtie index files (genome)..
[2014-07-28 10:47:10] Checking for reference FASTA file
[2014-07-28 10:47:10] Generating SAM header for hg19_indexes/hg19
[2014-07-28 10:48:45] Preparing reads
left reads: min. length=51, max. length=51, 25111234 kept reads (223 discarded)
right reads: min. length=51, max. length=51, 25084880 kept reads (26577 discarded)
[2014-07-28 10:58:49] Mapping left_kept_reads to genome hg19 with Bowtie2
[2014-07-28 11:29:21] Mapping left_kept_reads_seg1 to genome hg19 with Bowtie2 (1/2)
[2014-07-28 11:33:10] Mapping left_kept_reads_seg2 to genome hg19 with Bowtie2 (2/2)
[2014-07-28 11:38:02] Mapping right_kept_reads to genome hg19 with Bowtie2
[2014-07-28 12:09:08] Mapping right_kept_reads_seg1 to genome hg19 with Bowtie2 (1/2)
[2014-07-28 12:12:58] Mapping right_kept_reads_seg2 to genome hg19 with Bowtie2 (2/2)
[2014-07-28 12:18:00] Searching for junctions via segment mapping
[FAILED]
Error: segment-based junction search failed with err =-11
Loading left segment hits...
I am not getting why this error is coming.
Appreciate if anyone can help me to resolve this problem.
Thank you.
I think this could be a memory problem. Have you previously run tophat2 successfully? Can you try to run with only a subset of the reads?
Hi jon.brate,
Thank you for your reply.
But I am running through external hard disk.
No ... I haven't run tophat2 previously... This is the first time I am running.
subset of reads ??? I haven't got that.
"Memory" here probably means RAM memory, not disk space. How much RAM does your machine have?
RAM is 8 GB
Looking at this link makes it appear as that is borderline possible for the amount of reads you have. (something like 7GB for 20 million reads, about 15GB for 50 million reads).