In a RNA-seq dataset, I have two batches that have one sample in common, plus other samples in each batch. There are 3 replicates for each sample. Is there a way to compare other samples across tthe two batches? In other words, how can the batch effects be removed? The setup is shown above, how can I do DEG analysis to compare sample1 to sample3, or sample 2 to sample4?
Yes, you can perform DEG analysis across two batches with one shared sample by using batch correction methods like ComBat or limma. These tools help normalize batch effects while preserving biological differences. 7 brew locations