Comments (3)
I think this could be a field-specific analysis, and hence I would encourage you to create your own functions that take Milo/DA results and compute this. Milo is designed to facilitate DA testing, and it is necessary to be quite strict with what functionality is contained in the package because it also needs to be maintained (Heng Li I am not).
from milor.
You mean Aaron Lun? Heng Li hasn't maintained and improved bwa in years.
from milor.
Heng Li's comment on software devel: http://lh3.github.io/2019/03/11/on-maintaining-bioinformatics-software
(Also, I'm sure both Aaron and I would gladly agree that I'm not Aaron having worked with him for the best part of 3 years).
from milor.
Related Issues (20)
- Prevention of Neighbourhood Merging of Similar Cell Types into Neighbourhood Groups HOT 1
- Cell type is lost during annotateNhoods HOT 5
- Function Not Found Error HOT 3
- nhood size distribution: some neighbourhoods have over 2000 cells HOT 4
- Progress Bar for GLMM HOT 6
- object 'as.SimpleList' of mode 'function' was not found when running calcNhoodDistance HOT 2
- Multiple comparisons gives identical results by using model.contrasts HOT 12
- Does MiloR take into account that the two compared conditions have different number of cells? HOT 2
- Log10 FC or Log2 FC? HOT 1
- How to use MiloR after subsetting the cell types from total cell types? HOT 4
- Direction of test for logFC calculation HOT 1
- Existence of 2 tuitorials for the "Differential abundance testing with Milo - Mouse gastrulation example" HOT 3
- Import precomputed graph HOT 7
- makeNhoods graph refinement (issue with isolated vertices) HOT 4
- No Significant Neighbourhoods Result is Error HOT 1
- Mass cytometry data HOT 1
- MiloR in spatial transcriptomics data HOT 1
- Gene expression testing of only DA neighborhoods within group?? HOT 3
- Can you implement a complete miloR in python ? HOT 1
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