I was going to follow this method for my Salmon eq_classes files, but realized that with -i salmon_eq_classes for the first run, it turns off the -r option, so I do not get any .corset-read files from the first run (ie, one for each sample). All I get out are cluster and count files.
So is it possible to first consolidate assemblies for each sample using the Salmon eq-classes files? And then do a second run of corset across all the samples.
If not, do I have to write a huge list of assemblies (17) and samples (45)= 765 names in one command! I suppose I could also re-run it and make .bam files
Any suggestions would be appreciated!
Peter
https://groups.google.com/forum/#!topic/corset-project/ShzIVSWOWZk
Dear Nadia
Thanks for the tip. That makes a lot of sense. Now I’m wondering why I didn’t think of that earlier. And thanks for the quick response!
Best,
Peter
--
Peter Dunn
Dist. Professor
Dept of Biological Sciences
Univ. of Wisconsin-Milwaukee
PO Box 413
Milwaukee, WI 53201
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