Entering edit mode
10.5 years ago
ruansun1983
▴
40
Here is the problem
I have two paired read files, each with only 250 reads (so memory is not an issue)
the quality score is in illumina 1.8 format, has concerted to illumina 1.3 with command
sed -ie '4~4y/!"#$%&'\''()*+,-.\/0123456789:;<=>?@ABCDEFGHIJ/@ABCDEFGHIJKLMNOPQRSTUVWXYZ[\\]^_`abcdefghi/'
Then I run
tophat2 --solexa1.3-quals -r -70 --mate-std-dev 35 --library-type fr-firststrand -p 10 -o tophat_output allchr read1.fastq read2.fastq
which reported the following error
[2014-06-06 13:29:08] Beginning TopHat run (v2.0.11)
-----------------------------------------------
[2014-06-06 13:29:08] Checking for Bowtie
Bowtie version: 2.2.3.0
[2014-06-06 13:29:08] Checking for Samtools
Samtools version: 0.1.18.0
[2014-06-06 13:29:08] Checking for Bowtie index files (genome)..
Found both Bowtie1 and Bowtie2 indexes.
[2014-06-06 13:29:08] Checking for reference FASTA file
[2014-06-06 13:29:08] Generating SAM header for allchr
[2014-06-06 13:29:08] Preparing reads
left reads: min. length=101, max. length=101, 250 kept reads (0 discarded)
right reads: min. length=101, max. length=101, 250 kept reads (0 discarded)
[2014-06-06 13:29:08] Mapping left_kept_reads to genome allchr with Bowtie2
[FAILED]
Error running bowtie:
Error while flushing and closing output
terminate called after throwing an instance of 'int'
(ERR): bowtie2-align died with signal 6 (ABRT)
Removing --solexa1.3-quals
does not help
Can anyone help me?
Why not just keep the quality scores as is? You don't need to do anything special to get your fastq files to be handled properly.
original quality score report the same error. That is why I convert it
Try using a non-negative
-r
value. If that doesn't work, run the last command from the run log yourself and see if you get a different error.just tried, does not work. the same error