Hi,
I am pretty new to sequence analysis in general, but I was wondering if anyone know how to identify amplifications and deletions from 454 sequencing data? Intuitively, I would feel the coverage or read depth would indicate read depth (not sure about amplifications). But I'm not sure if this is the best way to go about it. Does anyone have any experience with this?
Thanks!
I am pretty new to sequence analysis in general, but I was wondering if anyone know how to identify amplifications and deletions from 454 sequencing data? Intuitively, I would feel the coverage or read depth would indicate read depth (not sure about amplifications). But I'm not sure if this is the best way to go about it. Does anyone have any experience with this?
Thanks!
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