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Hi everyone,
I have two scRNA‑seq datasets from different batches:
Dataset A: ~8,000 cells
Dataset B: ~60,000 cells
I want to integrate them to perform joint clustering and visualization.
Because the datasets differ so much in size, I’m unsure which strategy is most appropriate to:
Avoid the smaller dataset being dominated by the larger one
Correct batch effects effectively
Preserve biological signals
Could you please advise on the best method or workflow in Seurat 5 for this type of scenario?
Thank you very much for any guidance or examples
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