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-------- Original Message, Please send all replies to "all" --------

Hello Jennifer,
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.
Thanks.
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