Closed Chris-lang478 closed 1 year ago
Hi Christoph, I appreciate all your work. I have a question related to SingleR and Seurat objects.
I integrated two datasets using CCA-based method after scTransform normalization. The discussion in https://github.com/LTLA/SingleR/issues/98 is great to learn. In previous SCTransform,the team recomand to use raw counts with singleR and FindMarkers(https://github.com/satijalab/seurat/discussions/5605).
I read the paper for scTransform v2, With the release of SCTransform v2 ,the team recommend using the RNA or SCT assay ("data" slot) for performing DE.(https://satijalab.org/seurat/articles/sctransform_v2_vignette.html)
Is it right to use SCT assay produced by SCT v2 performing the cells annotations with singleR?Is there any more documentation about this?
In my cases I am integrating two samples from same tissues with different treatments to compare cell types between them.
Thanks!
I dunno who Christoph is, but see #98.
Hi Christoph, I appreciate all your work. I have a question related to SingleR and Seurat objects.
I integrated two datasets using CCA-based method after scTransform normalization. The discussion in https://github.com/LTLA/SingleR/issues/98 is great to learn. In previous SCTransform,the team recomand to use raw counts with singleR and FindMarkers(https://github.com/satijalab/seurat/discussions/5605).
I read the paper for scTransform v2, With the release of SCTransform v2 ,the team recommend using the RNA or SCT assay ("data" slot) for performing DE.(https://satijalab.org/seurat/articles/sctransform_v2_vignette.html)
Is it right to use SCT assay produced by SCT v2 performing the cells annotations with singleR?Is there any more documentation about this?
In my cases I am integrating two samples from same tissues with different treatments to compare cell types between them.
Thanks!