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how to analyze and summarize multiple whole-exome-sequencing studies

Hi everyone, there are several similar whole-exome-sequencing studies published in the same disease. I would like to summarize them. However, i don't want to just describe or list what they found. I know we can do a meta-analysis to combine data from different studies. Is there any similar method to integrate whole-exome-sequencing results?

Thanks April

next-gen

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