Hi everyone,
I would like to use several CNV tools on a common dataset and compare the results.
How should I go about simulating a genome with CNVs in known positions? I know how to simulate reads from a 'normal' genome, but I was wondering if there was a tool out there that will 'insert' CNVs into a normal genome.
Any help/comments will be much appreciated.
Thanks!
I would like to use several CNV tools on a common dataset and compare the results.
How should I go about simulating a genome with CNVs in known positions? I know how to simulate reads from a 'normal' genome, but I was wondering if there was a tool out there that will 'insert' CNVs into a normal genome.
Any help/comments will be much appreciated.
Thanks!
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