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What tools do you use in Basepair's single cell pipeline?
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Can I upload two samples of single cell RNA-seq data (treatment and control) and compare them?
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How do you account for technical variability? Does the program fit for mean variance trend, test for non zero biological variability, or deconvolution based normalization?
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Do you check the relationship between nUMI vs nGenes plot? Do you have a specific threshold in this graph?