Dear mira users, I just received some sff files from our sequence facility, so dutifully, I ran sff_extract and produced a nice fastq / xml file set ready for MIRA. MIRA crashed with a "Sanity check of read '<insert read name here>' failed" error. I went and looked at the failed sequence and sure enough, it was crap. So I fired up emacs and removed the offending entry, and yes, it happened again. I don't particularly want to remove bad sequences using the "fail by crashing mira" followed by "edit using emacs" approach. Before I go and try and write code to examine and filter out bad fastq data, is there something obvious out there that I could use? Thanks John -- You have received this mail because you are subscribed to the mira_talk mailing list. For information on how to subscribe or unsubscribe, please visit http://www.chevreux.org/mira_mailinglists.html