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This function performs doublet-calling using the scrublet(python) package on a Seurat object.

Usage

db_Scrublet(srt, assay = "RNA", db_rate = ncol(srt)/1000 * 0.01, ...)

Arguments

srt

A Seurat object.

assay

The name of the assay to be used for doublet-calling. Default is "RNA".

db_rate

The expected doublet rate. Default is calculated as ncol(srt) / 1000 * 0.01.

...

Additional arguments to be passed to scrublet.Scrublet function.

Examples

data(pancreas_sub)
pancreas_sub <- standard_scop(pancreas_sub)
#>  [2025-09-20 14:02:46] Start standard scop workflow...
#>  [2025-09-20 14:02:47] Checking a list of <Seurat> object...
#> ! [2025-09-20 14:02:47] Data 1/1 of the `srt_list` is "unknown"
#>  [2025-09-20 14:02:47] Perform `NormalizeData()` with `normalization.method = 'LogNormalize'` on the data 1/1 of the `srt_list`...
#>  [2025-09-20 14:02:50] Perform `Seurat::FindVariableFeatures()` on the data 1/1 of the `srt_list`...
#>  [2025-09-20 14:02:50] Use the separate HVF from srt_list
#>  [2025-09-20 14:02:50] Number of available HVF: 2000
#>  [2025-09-20 14:02:51] Finished check
#>  [2025-09-20 14:02:51] Perform `Seurat::ScaleData()`
#> Warning: Different features in new layer data than already exists for scale.data
#>  [2025-09-20 14:02:51] Perform pca linear dimension reduction
#> StandardPC_ 1 
#> Positive:  Aplp1, Cpe, Gnas, Fam183b, Map1b, Hmgn3, Pcsk1n, Chga, Tuba1a, Bex2 
#> 	   Syt13, Isl1, 1700086L19Rik, Pax6, Chgb, Scgn, Rbp4, Scg3, Gch1, Camk2n1 
#> 	   Cryba2, Pcsk2, Pyy, Tspan7, Mafb, Hist3h2ba, Dbpht2, Abcc8, Rap1b, Slc38a5 
#> Negative:  Spp1, Anxa2, Sparc, Dbi, 1700011H14Rik, Wfdc2, Gsta3, Adamts1, Clu, Mgst1 
#> 	   Bicc1, Ldha, Vim, Cldn3, Cyr61, Rps2, Mt1, Ptn, Phgdh, Nudt19 
#> 	   Smtnl2, Smco4, Habp2, Mt2, Col18a1, Rpl12, Galk1, Cldn10, Acot1, Ccnd1 
#> StandardPC_ 2 
#> Positive:  Rbp4, Tagln2, Tuba1b, Fkbp2, Pyy, Pcsk2, Iapp, Tmem27, Meis2, Tubb4b 
#> 	   Pcsk1n, Dbpht2, Rap1b, Dynll1, Tubb2a, Sdf2l1, Scgn, 1700086L19Rik, Scg2, Abcc8 
#> 	   Atp1b1, Hspa5, Fam183b, Papss2, Slc38a5, Scg3, Mageh1, Tspan7, Ppp1r1a, Ociad2 
#> Negative:  Neurog3, Btbd17, Gadd45a, Ppp1r14a, Neurod2, Sox4, Smarcd2, Mdk, Pax4, Btg2 
#> 	   Sult2b1, Hes6, Grasp, Igfbpl1, Gpx2, Cbfa2t3, Foxa3, Shf, Mfng, Tmsb4x 
#> 	   Amotl2, Gdpd1, Cdc14b, Epb42, Rcor2, Cotl1, Upk3bl, Rbfox3, Cldn6, Cer1 
#> StandardPC_ 3 
#> Positive:  Nusap1, Top2a, Birc5, Aurkb, Cdca8, Pbk, Mki67, Tpx2, Plk1, Ccnb1 
#> 	   2810417H13Rik, Incenp, Cenpf, Ccna2, Prc1, Racgap1, Cdk1, Aurka, Cdca3, Hmmr 
#> 	   Spc24, Kif23, Sgol1, Cenpe, Cdc20, Hist1h1b, Cdca2, Mxd3, Kif22, Ska1 
#> Negative:  Anxa5, Pdzk1ip1, Acot1, Tpm1, Anxa2, Dcdc2a, Capg, Sparc, Ttr, Pamr1 
#> 	   Clu, Cxcl12, Ndrg2, Hnf1aos1, Gas6, Gsta3, Krt18, Ces1d, Atp1b1, Muc1 
#> 	   Hhex, Acadm, Spp1, Enpp2, Bcl2l14, Sat1, Smtnl2, 1700011H14Rik, Tgm2, Fam159a 
#> StandardPC_ 4 
#> Positive:  Glud1, Tm4sf4, Akr1c19, Cldn4, Runx1t1, Fev, Pou3f4, Gm43861, Pgrmc1, Arx 
#> 	   Cd200, Lrpprc, Hmgn3, Ppp1r14c, Pam, Etv1, Tsc22d1, Slc25a5, Akap17b, Pgf 
#> 	   Fam43a, Emb, Jun, Krt8, Dnajc12, Mid1ip1, Ids, Rgs17, Uchl1, Alcam 
#> Negative:  Ins2, Ins1, Ppp1r1a, Nnat, Calr, Sytl4, Sdf2l1, Iapp, Pdia6, Mapt 
#> 	   G6pc2, C2cd4b, Npy, Gng12, P2ry1, Ero1lb, Adra2a, Papss2, Arhgap36, Fam151a 
#> 	   Dlk1, Creld2, Gip, Tmem215, Gm27033, Cntfr, Prss53, C2cd4a, Lyve1, Ociad2 
#> StandardPC_ 5 
#> Positive:  Pdx1, Nkx6-1, Npepl1, Cldn4, Cryba2, Fev, Jun, Chgb, Gng12, Adra2a 
#> 	   Mnx1, Sytl4, Pdk3, Gm27033, Nnat, Chga, Ins2, 1110012L19Rik, Enho, Krt7 
#> 	   Mlxipl, Tmsb10, Flrt1, Pax4, Tubb3, Prrg2, Gars, Frzb, BC023829, Gm2694 
#> Negative:  Irx2, Irx1, Gcg, Ctxn2, Tmem27, Ctsz, Tmsb15l, Nap1l5, Pou6f2, Gria2 
#> 	   Ghrl, Peg10, Smarca1, Arx, Lrpap1, Rgs4, Ttr, Gast, Tmsb15b2, Serpina1b 
#> 	   Slc16a10, Wnk3, Ly6e, Auts2, Sct, Arg1, Dusp10, Sphkap, Dock11, Edn3 
#>  [2025-09-20 14:02:52] Perform `Seurat::FindClusters()` with louvain and `cluster_resolution` = 0.6
#>  [2025-09-20 14:02:52] Reorder clusters...
#> ! [2025-09-20 14:02:52] Using `Seurat::AggregateExpression()` to calculate pseudo-bulk data for <Assay5>
#>  [2025-09-20 14:02:52] Perform umap nonlinear dimension reduction
#>  [2025-09-20 14:02:52] Non-linear dimensionality reduction (umap) using (Standardpca) dims (1-50) as input
#>  [2025-09-20 14:02:52] UMAP will return its model
#>  [2025-09-20 14:02:57] Non-linear dimensionality reduction (umap) using (Standardpca) dims (1-50) as input
#>  [2025-09-20 14:02:57] UMAP will return its model
#>  [2025-09-20 14:03:02] Run scop standard workflow done
pancreas_sub <- db_Scrublet(pancreas_sub)
#>  [2025-09-20 14:03:02] Data type is raw counts
#>  [2025-09-20 14:03:04] Checking 1 packages in environment: scop_env
#>  [2025-09-20 14:03:05] Retrieving package list for environment: scop_env
#>  [2025-09-20 14:03:07] Found 200 packages installed
#> ! [2025-09-20 14:03:07] scrublet not found
#>  [2025-09-20 14:03:07] Try to install: scrublet
#>  [2025-09-20 14:03:07] Installing 2 packages into environment: scop_env
#>  [2025-09-20 14:03:08] Installing packages via pip...
#>  [2025-09-20 14:03:12] pip installation completed
#>  [2025-09-20 14:03:13] Checking 1 packages in environment: scop_env
#>  [2025-09-20 14:03:14] Retrieving package list for environment: scop_env
#>  [2025-09-20 14:03:16] Found 205 packages installed
#>  [2025-09-20 14:03:16] scrublet version: 0.2.3
CellDimPlot(
  pancreas_sub,
  reduction = "umap",
  group.by = "db.Scrublet_class"
)
#> Warning: No shared levels found between `names(values)` of the manual scale and the
#> data's fill values.

FeatureDimPlot(
  pancreas_sub,
  reduction = "umap",
  features = "db.Scrublet_score"
)