There is nice Python lib : https://pypi.org/project/infercnvpy/ which infers copy number variations from the single-cell RNA seq data. But it requires Python 3.8 and on free clouds like colab (or kaggle) one has 3.7.1
Question: Is there infer CNV like python library which works for Python 3.7.1 (colab/kaggle) ?
Or there can be other ways round ?
Here is link to problem example notebook: