metalsinglecell.pp.scale#
- metalsinglecell.pp.scale(adata, max_value=None, zero_center=True, layer=None, copy=False)[source]#
Z-score genes then clip (
sc.pp.scale). Densifies (zero-centering breaks sparsity).max_valuedefaults toNone(no clip), matching scanpy/rapids-singlecell — pass a value (e.g. 10) to clip z-scores, as the atlas/streaming demos do explicitly.