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Old 01-22-2018, 11:02 AM   #1
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Default NSG to detect deletions and duplications genome-wide

hi there,

I need to detect deletions and duplications genome-wide in human cells. ideally I would like to use several clones (the more the better) and detect the number of deletions and duplications in each clone. is there an easy way to do that with NSG instead of classical tiling array CGH?

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