Comments (2)
Don't forget to add a lfc=
option for pairwiseWilcox()
; this could probably be co-opted from tol=
.
from scran.
- return unsorted output from
findMarkers
. This should allow you to just do the following for collating results into a single table.
markers.pbmc.up <- findMarkers(sce.pbmc, sce.pbmc$cluster, direction="up", log.p=TRUE)
x <- DataFrame(
row.names = rownames(sce.pbmc),
lapply(markers.pbmc.up, "[[", i="log.FDR")
)
from scran.
Related Issues (20)
- Different list for findmarker function HOT 1
- scran normalize HOT 1
- Depreciated scran functions and commands. Any updated tutorial?
- Error normalizing Anndata
- Old versions disappeared from bioconductor? HOT 3
- cant load scran HOT 6
- Error in FUN(x, table, nomatch = nomatch, incomparables = incomparables) : 'match' requires vector arguments HOT 2
- DEG results only contain downregulated gene HOT 2
- `scoreMarkers()`: Parallelisation changes `rank.*` statistics HOT 2
- findMarkers produces unexpectedly different results with passing different values to direction HOT 11
- Installation of package ‘scran’ had non-zero exit status HOT 2
- findmarkers summary.logFC values HOT 1
- `pseudoBulkDGE()` intermediates dropped if `row.data` supplied HOT 1
- Installation is failing HOT 6
- error using scaledColRanks HOT 3
- Add lfc= option back to scoreMarkers
- Error in (function (classes, fdef, mtable) : unable to find an inherited method for function ‘assay’ for signature ‘"dgRMatrix", "character"’ HOT 1
- BiocParallel errror (invalid length of row names) in combineMarkers() with full.stats = TRUE HOT 2
- Cyclone not finishing when using BPPARAM=MulticoreParam(workers = n))
- Receiving 'ref.clust' not in 'clusters' for cluster label that is part of predefined clusters HOT 5
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from scran.