Monopogen
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openCRAVAT application
Good morning, Thank you very much for the help provided previously. I am trying to use the output derived from the somatic module, i.e. chr.SNV_mat.RDS in the openCRAVAT software but to do so I would need to better understand the data output. In fact, a necessary field in the openCRAVAT input file is: Strand The strand the variant is on. Either '+' (plus strand): Indicates that the genetic variant is located on the positive (or sense) strand or '-' (minus strand): Indicates that the variant is located on the negative (or anti-sense) strand. Is there any way to know this information or maybe since it's RNA I have to act differently?
Any help is appreciated Thank you