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Old 07-27-2011, 02:07 PM   #15
Compendia Bio
Location: Ann Arbor

Join Date: Oct 2010
Posts: 35

Originally Posted by louis7781x View Post
Thanks for your help,I want to know the input type because the coverage of DNA-seq and RNA-seq is different.So if I use RNA-seq aligned to ref genome and use output file bam to run CNV-seq,Does it apply to analyze copy number varivation?
I have the same question too. It would be really great if someone can shed some light on it.
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