That seems reasonable. Will I be able to keep track of which condition cells came from within the matrix? If so, how?
Combining Conditions in scRNA-seq (Drop-seq) for Analysis
Hi,
I recently ran a Drop-seq experiment and got my demultiplexed data back for two different conditions. When should I combine the two files together? I began with two queryname-sorted BAM files. Should I merge the files after alignment, right before alignment, or after I extract the matrix for each condition?
Thanks
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For PCA (or tSNE, which is likely what you'll end up doing), you'll need a matrix with all of the cells for both conditions. Don't "merge" things in any other way.
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Normally you just cbind() them and will know beforehand how many come from each cell type, so yes. But the responsibility for doing that is on you.
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What's the goal? I assume you have multiple cells for each condition and are able to get counts for each. Normally you'll be using a matrix of that.
Yes, there are many cells for each condition, but I want to plot both conditions onto one plot (probably a PCA plot).