I’ve been running into some unexpected errors with my recent DNA sequencing projects — specifically, I’ve noticed issues with low quality reads despite strict sample prep protocols. Has anyone experienced similar challenges? I’m curious about your troubleshooting approaches and any tips you might have.
I’ve seen low quality reads when using older reagents; have you checked theirs? Sometimes it’s worth trying fresh samples too. @labtechsupport could offer more insights.
Have you considered optimizing your library prep — sometimes reducing input DNA can help with read quality. @james_tech87, what do you think?