Hi,<br>  I believe you have to run Fastq Groomer first to convert it to sanger format. Then you will be able to see your dataset. <br><br><a href="https://main.g2.bx.psu.edu/u/dan/p/fastq">https://main.g2.bx.psu.edu/u/dan/p/fastq</a><br>
<br>Best,<br><br>Luciano<br>