Let me reply to my own question:
What happened is that the solid2fastq script obviously did not process the reads completely (as a part of the batch process).
Funnily enough, the last read of the fastq file being incomplete did not prevent bwa aln to run and generate a .sai file.
Only in the bwa samse step, this caused trouble and led to said error message.
Hope this helps.
cheers,
Sophia
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Dear all,
I got this error message, too, when running bwa samse (bwa-0.5.9rc1):
Code:[bwa_aln_core] refine gapped alignments... Segmentation fault (core dumped)
1. my original SOLiD reads were reformatted using bwa's solid2fastq.pl alright, and
2. I ran a batch of 12 samples that were processed all the same way. Only 7 gave this error, 5 were processed without error.
Any ideas why this happens will be appreciated.
thanks,
Sophia
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Thank you for your help.
I was just too stupid for reading the manual. I did new indexing of the genome with the -a is argument which is not recommended for large genomes. After applying the -a bwt option in indexing, alignment worked.
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I had the same problem (BWA on Fedora 13) and gave up on it for a long time. Then someone passed me a BLOG link:
Here's what I use for bwa alignment (without removing PCR dups). You can replace the paths with your own and put into a bash script for au...
My problem seemed to be i was using a solid2fastq script from a different program (BFAST i think. Why was i doing this, because it is C-compiled therefore much faster!). Once i used solid2fast from the BWA package it started working.
I hope this helps!
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BWA crashes in Fedora
Lately I changed OS from Ubuntu to Fedora (KDE) (both 64bit).
While in Ubuntu BWA worked perfectly it now crashes while trying to align a 7.4GB Illumina fastQ file which I could align perfectly in Ubuntu.
The output is
Code:[bwa_aln] 17bp reads: max_diff = 2 [bwa_aln] 38bp reads: max_diff = 3 [bwa_aln] 64bp reads: max_diff = 4 [bwa_aln] 93bp reads: max_diff = 5 [bwa_aln] 124bp reads: max_diff = 6 [bwa_aln] 157bp reads: max_diff = 7 [bwa_aln] 190bp reads: max_diff = 8 [bwa_aln] 225bp reads: max_diff = 9 [bwa_aln_core] calculate SA coordinate... Segmentation fault (core dumped)
The command was:
Code:bwa aln ~/RefSeq/hg19_070510/Chromosomes/hg19.fa test.fq > test.aln
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