Is it possible to confidently carry out CNV analysis using whole exome sequencing data? There are many papers now that suggest it is possible, but how confident can we be about the results? And when using older BAM files to carry out this CNV analysis, is there a possibility that newer tools will experience more errors because of incompatibility of data files and software?
Question: CNV analysis from exome sequencing data
17 months ago by
mkamranazim • 0
mkamranazim • 0 wrote:
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