Hi,
I used ExomeCNV and FREEC on my tumor-normal matched exome sequencing samples to discover copy number variations. Now I need to combine and annotate the results.
What kind of tools would you suggest for the task ?
Can Annovar be used for annotation purpose of CNV files?
Thanks
Suleyman
I used ExomeCNV and FREEC on my tumor-normal matched exome sequencing samples to discover copy number variations. Now I need to combine and annotate the results.
What kind of tools would you suggest for the task ?
Can Annovar be used for annotation purpose of CNV files?
Thanks
Suleyman
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