By default, when demultiplexing with CASAVA, same sample across multiple lanes is added to separate FASTQ file for each lane. Is there a way to have one FASTQ file for each sample?
There is a --fastq-cluster-count option so that FASTQs are not limited to a certain amount of reads. Maybe there is something to make FASTQs not limited to one lane?
There is a --fastq-cluster-count option so that FASTQs are not limited to a certain amount of reads. Maybe there is something to make FASTQs not limited to one lane?
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