I have a mIHC dataset that has information on the different cells present in each sample based on the biomarker association they show. this dataset has pre-treatment and post-treatment data with 2 panels in each having different sets of biomarker each panel (its not entirely different, some are common). Each panel has 2 type of data, being whole number of cells and relative number of cells in percentage. I am confused as to use PLS-DA on each of the panels or p integration on the 2 panels.
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