-------- Original Message, Please send all replies to "all" --------
I am a new to Linux and have no programming skills and hence galaxy is
the only rescuer for me.
I have nextgen dna seq data. I finished analysis and now have a list of
variants. I want to see if these variants are already in 1000 genome
data released in Aug 2011. I want to upload list of my chromosome
locations and see if they are any matches with 1000 genome data.
IS there a way we can do it in galaxy...instead of writing scripts to do
it. Like I said, I have no programming skills.
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