Hi,
I believe you have to run Fastq Groomer first to convert it to sanger
format. Then you will be able to see your dataset.
https://main.g2.bx.psu.edu/u/dan/p/fastq
Best,
Luciano
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Luciano Cosme cosme.sim...@gmail.com wrote:
Hi,
I believe you have to run Fastq Groomer first to convert it to sanger format.
Then you will be able to see your dataset.
https://main.g2.bx.psu.edu/u/dan/p/fastq
Best,
Luciano
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