Comments (2)
Hi, I believe using count based data for training is more acceptable, that is because 1. Since there are missing genes in the spatial data, we cannot directly normalize the raw count spatial data. 2. Tangram does not have specific distribution modeling for input data.
But I think Xenium has large-scale spots and it is hard for me to place tangram in my gpu node. Do you use the cpu version to train your model? Thanks.
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Hi @mortunco , one restriction of Tangram is that the cell type compositions between the scRNA-seq and spatial need to be similar. For Q2, how does the cell type composition compare between the sc and spatial? And another question is that how does the gene prediction behavior looks like overall? Can you help to plot the cos_sim vs sparsity of the gene as in the tutorial.
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Related Issues (20)
- Can we have an API as batch size for the integration method? HOT 3
- No attribute 'pp_adatas' in tangram HOT 2
- Possible to use multiple single cell datasets in Tangram? HOT 3
- Cannot find correspondence of the input data HOT 1
- question about training genes HOT 1
- Some questions about best practices HOT 1
- Attribute error : module 'tangram' has no attribute 'map_cells_to_space' HOT 2
- scRNAseq cells < spatial cells, curious about how mapping works HOT 3
- Unexpected behaviour HOT 1
- Question about acceptable AUC, improving AUC HOT 1
- potential overfitting HOT 5
- Interpretation of tangram_ct_pred HOT 2
- Option "enforce gene lowercase" HOT 1
- error when sq.im.segment
- Tangram Deconvolution HOT 1
- Using Integrated single cell data for alignment
- AttributeError: module 'tangram' has no attribute 'pp_adatas'
- Sparsity_sc and sparsity_sp = 0
- Please explain `project_cell_annotations`
- Running time for Tangram
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