Hi there,
We are re-analyzing several Solexa Fastq files generated during the past couple of years. They were not all created on the same version of the Illumina Genome Analyzer pipeline. Does anyone know of a straightforward (and perhaps automatic?) way to recognize the precise fastq format so we can analyze these data appropriately?
Many thanks.
We are re-analyzing several Solexa Fastq files generated during the past couple of years. They were not all created on the same version of the Illumina Genome Analyzer pipeline. Does anyone know of a straightforward (and perhaps automatic?) way to recognize the precise fastq format so we can analyze these data appropriately?
Many thanks.
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