Closed yojetsharma closed 1 month ago
Hi there - our recommendation is to follow the initial processing and QC'ing for RNA using Seurat, and ATAC using Signac (for example), in order to get the normalized gene x cell (RNA) and peak x cell (ATAC) matrices in order. Once you've done this, you can extract the input objects for FigR analysis as mentioned in this earlier issue comment: https://github.com/buenrostrolab/FigR/issues/18#issuecomment-1385915205
Let me know if this helps
I went through both the vignettes that are available. However, I was wondering if there was more on how to generate the .rds files for scRNA (sparsematrix) and scATAC seq (SummarizedExperiment).