Closed rocketeer1998 closed 2 years ago
Hi @rocketeer1998 , thanks for the feedback! Can you please specify, what exactly do you want to get as an output?
Hi @rocketeer1998 , thanks for the feedback! Can you please specify, what exactly do you want to get as an output?
Just as shown in your publication Fig.6 e and f. I want to show the spatial distribution of some cell types based on marker gene expression.
The annotation for that was done manually, and the plot just shows each cell as a dot, so we don't have the code for that in the package. To do the same, you can take cell positions from segmentation_cell_stats.csv
and match it with segmentation_counts.tsv
to get cell markers.
The annotation for that was done manually, and the plot just shows each cell as a dot, so we don't have the code for that in the package. To do the same, you can take cell positions from
segmentation_cell_stats.csv
and match it withsegmentation_counts.tsv
to get cell markers.
OK. Thanks a lot!
Hi, @VPetukhov. First of all, thanks for the convenience the
Baysor
has brought to my ISS study. After a fullbaysor run
, I have obtained a beautiful cell segmentation plot and a useful expression matrix that I can use in the downstream scRNA-seq analysis.As for scRNA-seq analysis tool, I think
Seurat
is stabler and more robust thanpagoda2
, though the latter provides a convenient web app to analyze my data. So I want to perform a standard scRNA-seq pipeline usingSeurat
and label each cell with a cell type. So is there any recommendation about projecting this result back to the cell segmentation plot created byBaysor
? Otherwise, I have to simulate a segmentation plot using ggplot2.Thanks for your kind reply!