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Old 02-04-2013, 07:59 PM   #2
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Location: Québec, Canada

Join Date: Jul 2008
Posts: 258

Originally Posted by stepa_t View Post
Dear all!
I've tried to use Reprile error correction tool ( ) for my MiSeq reads, but unfortunately this soft cannot read my fastq file, despite this file was OK with FastQC and different assemblers. Do you know if there is any modification in fastq format in MiSeq versus other Illumina sequencers, since supposedly it was tested only on GA data? Is there any FastQ file converters?
Does the documentation of Reptile say anything about compatibility with FastQ ?

Can you post the result of this:

$ head myFastqFile.fastq

Maybe your reads are too long, who knows.
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