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Hi, Thanks, |
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Hi,
I'm working through the vignette on WNN and 10X multiome data. My dataset consists of two conditions of two replicates each (ie ATAC1+ATAC2+RNA1+RNA2 for a condition), and I'd like to perform integration of the data to correct for collection batch effects. Would it be best to run integration of each assay across the suerat objects or is there a better way to perform integration that includes both the ATAC and RNA data all at once?
Thanks.
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