Closed liaoshengguang closed 1 year ago
1) The number of markers needed will depend on the specificity of the markers selected. In general I would recommend using 10-100 markers.
2) Setting these parameters is dataset specific and it's hard to provide specific guidelines. In general I find it useful to examine the strength of the metrix when for a classification that is likely correct and compare this to a classification that is likely incorrect. For most datasets you'll likely have one or more clusters that are clearly identifiable as a known cell type that should occur in the dataset. Compare the classification values for these clusters, to the classification values returned for correlations against a cell type that should not be present in the data. The spread between these values can help with defining cutoffs.
@raysinensis may have some additional guidance to share.
Hello, thanks for this wonderful package. I am trying to annotate my clusters with the known marker genes with clustify_lists function.
i have two questions:
Many thanks.