Hello
i have a pipeline which works with illumina reads. When i convert the 454 reads in to fastq format and give it as input, the pipeline is not working. The average length of the sequence is 350 bp. I am planning to make them in to 100bp reads. Are there any tools out there which can do this?
i have a pipeline which works with illumina reads. When i convert the 454 reads in to fastq format and give it as input, the pipeline is not working. The average length of the sequence is 350 bp. I am planning to make them in to 100bp reads. Are there any tools out there which can do this?
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