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Combining datasets from different sequencing platforms

Hello,

I'm trying to analyze a whole exome sequencing data with cases-only. I have an external dataset that will be potentially used as a control group. The problem is the external data is imputed array data. I'm wondering if I can combine the two datasets and how to show their compatibility. Thank you for any helps in advance.

analyses

It is going to be very challenging to figure out what differences between your control and your cases is biological, and what differences are caused by batch effect and using a totally different technology.

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