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Hi, I have a question for using immunarch for TCR analysis with 2 (or more) different bulk-seq results.
Is it possible to compare TCR diversity from different experiment sets and is there any way for batch correction? or is it impossible.
Thanks
The text was updated successfully, but these errors were encountered:
Thank you for opening the issue. You could put all data in your_data$data and update the metadata table in your_data$meta to reflect changes. As a possible way to make sure the data is "normalized", you could use repSample to downsample the data to the smallest dataset volume. I don't think there are other possible ways to do a batch correction. Did you use different technologies to get the data?
I'm open to scheduling a short call to discuss this issue over Zoom if this accelerates things.
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Hi, I have a question for using immunarch for TCR analysis with 2 (or more) different bulk-seq results.
Is it possible to compare TCR diversity from different experiment sets and is there any way for batch correction? or is it impossible.
Thanks
The text was updated successfully, but these errors were encountered: