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Old 07-14-2011, 12:05 PM   #1
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Default BFAST match abort trap


I am trying to analyze SOLiD data using BFAST, and am a little new to the system. I have successfully created and indexed the reference genome, but I am running into problems with BFAST match. I get an error message saying:

Reading /ResearchFiles/JEC21_genome/CNA_assembly/BFAST/NIH433_fastq_reads.1.fastq into a temp file.
Assertion failed: (m->readLength > 0), function RGMatchPrint, file ../bfast/RGMatch.c, line 155.
Abort trap

My command line is bfast match -f JEC21_all.fasta -r NIH433_fastq_reads.1.fastq > NIH433_JEC21_matched

I also created the input fastq file using the solid2fastq program that came with the BFAST package.

Any idea what is causing this?


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Old 07-14-2011, 07:29 PM   #2
Nils Homer
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Most likely the input fastq is corrupted. You can either try to re-run solid2fastq, or remove reads from the input fastq until you find the offending read.
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