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Thread | Thread Starter | Forum | Replies | Last Post |
BFAST - Help | cutcopy11 | SOLiD | 17 | 10-17-2013 08:12 AM |
BFAST fasta2brg help | Esther | Bioinformatics | 4 | 05-10-2011 01:29 PM |
BFAST bfast.submit.pl configuration | epigen | Bioinformatics | 1 | 03-18-2011 07:51 AM |
BFAST thanks you for your help! (was: ... needs your help) | nilshomer | Bioinformatics | 5 | 04-21-2010 08:29 PM |
Bfast | jsun529 | Bioinformatics | 19 | 11-12-2009 09:32 AM |
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#1 |
Member
Location: Hoboken, NJ Join Date: May 2011
Posts: 15
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Hi,
I'm working on my thesis work and I'm trying to run BFAST software for aligning FASTQ datasets. I'm getting error written below. and the command is; > bfast fasta2brg -f filename The error is; ________________________________________________________________ **************** Checking input parameters supplied by the user ... Validating fastaFileName SRR035022_1.filt.fastq. Input arguments look good! **************** Printing Program Parameters: programMode: [ExecuteProgram] fastaFileName: SRR035022_1.filt.fastq space: [NT Space] timing: [Not Using] ****************** Reading from SRR035022_1.filt.fastq. ******************** In function "RGBinaryRead": Fatal Error[OpenFileError]. Variable/Value: SRR035022_1.filt.fastq. Message: Could not open file for reading. The file stream error was:: Value too large for defined data type ***** Exiting due to errors ***** _____________________________________________________________ I couldnt figure out what the problem is... Can you tell me what I'm doing wrong ? Thanks in advance... |
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