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atgc · 06-18-2011, 09:13 PM

Hello,

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.

ATGC

06-18-2011, 09:13 PM	#1
atgc Junior Member Location: California Join Date: Aug 2010 Posts: 6	Mapping and base calling Hello, 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. ATGC