Closed davetang closed 6 years ago
Hi, thanks for your question! The short answer is: yes, if you don't like the results of M3Drop you can select features manually by defining the scmap_features
vector in the rowData
slot:
rowData(YOUR_SCE_OBJECT)$scmap_features <- YOUR_VECTOR
scmap_features
values must be either TRUE
or FALSE
corresponding to selected and non-selected genes accordingly. This should be sufficient for your purposes, but please let me know if there are any errors.
Brilliant, thanks!
Hi there! Thank you for the very useful package. I have a question on
selectFeatures
and whether other methods, such as using highly variable genes, will be implemented? I realise that the M3Drop preprint suggests that it out performs other feature selection methods, at least in full-transcript scRNA-seq protocols (I have UMI data by the way). If I want to implement something myself, is it simply defining a logical vector toscmap_features
for the genes I want to use?My problem is that the M3Drop method doesn't identify representative genes that define one of my clusters and hence even when I project the data onto itself, only half of the cells in that cluster are assigned back to that cluster. I've tried increasing the number of features/genes up to 2,000 but it doesn't improve.