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Old 04-18-2013, 12:37 PM   #1
Location: Cambridge

Join Date: Apr 2013
Posts: 32
Default CASIM: Variants, Detecting Aneuploidy

Whatís the best way of detecting aneuploidy in a whole genome data set?

Is read depth all that there is? Can we detect and use alterations in chromosomal SNP rates?

Any better approach?
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