I am using a transcriptome and a cegma annotation to run the first maker
iteration. Based on the resulting genes I build a snap model and start
the second iteration. The transcriptome and the cegma annotation are
passed through. What is the option est2genome (set to 1) doing in this
case? Is it somehow preferred over any other prediction method? Is it
useful to switch on several predictors during one run? And my last
question, if the switch for repeat masking pass through is on does this
mean that maker is not running any rm computations?
best regards
felix
--
Felix Bemm
Department of Bioinformatics
University of Würzburg, Germany
Tel: +49 931 - 31 83696
Fax: +49 931 - 31 84552
felix...@uni-wuerzburg.de
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