On Tue, Jun 24, 2014 at 11:16 PM, Bastien Chevreux <bach@xxxxxxxxxxxx> wrote: > >> (a) All in one file (using the read names to spot pairs, fine for >> MIRA input). > > I hope you meant “output to one file”. That’s in. Yes, I mean as output (since MIRA is able to take this as input?). > If you meant “i have one big unsorted file with pairs and singlets > mixed” as input … that’s currently not foreseen and I’m not sure > I want to implement that. There’s one read-naming hell awaiting > … how to correctly parse out template names if, e.g., Sanger, > 454 and Illumina are mixed in one FASTQ file? > > Any good use case in mind? This could be useful if your paired data has been through any non-pair preserving QC or filtering step (e.g. the old mirabait). But I appreciate this is a complex job, and insisting on nicely paired input makes sense. Peter -- 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