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Old 06-18-2011, 09:13 PM   #1
Junior Member
Location: California

Join Date: Aug 2010
Posts: 6
Default Mapping and base calling


I recently received sequencing data from Illumina's HiSeq. The reads are 100 bp, paired end. The data has been provided to us in fastq format.

I have worked with PE sequencing earlier. However, initially, data was provided in a txt format which we imported into CLC Genomics Workbench. Does anyone know if the fastq format can be imported into CLC Genomics Workbench?
Thanks for your help in advance.

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