chord | R Documentation |
remove doublet with scds,bcds,DoubletFinder.
chord( seu = NA, sce = NA, doubletrate = NA, mfinal = 40, k = 20, method = "gbm", overkill = T, overkillrate = 1, outname = "out", seed = 1, addmethods1 = NA, addmethods2 = NA, overkilllist = NA, adddoublt = NA, cxds.ntop = NA, cxds.binThresh = NA, bcds.ntop = NA, bcds.srat = NA, dbf.PCs = 1:10, dbf.pN = 0.25, dbf.pK = NA )
seu |
the input sce object |
mfinal |
an integer, the number of iterations for which boosting is run or the number of trees to use. Defaults to mfinal=40 iterations.(only works when method="adaboost") |
k |
an integer,k-means param k |
method |
the boost method ("adaboost" or "gbm") |
overkill |
if True,use overkill |
overkillrate |
an integer,remove the top ?% doublet-liked cells of any methods' results.(0-1) |
outname |
The prefix of the output file |
seed |
an integer, random seed |
addmethods1 |
the table merged with other method's scores1 |
addmethods2 |
the table merged with other method's scores2 |
overkilllist |
a vector of cells to be remove in overkill |
adddoublt |
doubletrate of cells to be simulate |
cxds.ntop |
integer, indimessageing number of top variance genes to consider. Default: 500 |
cxds.binThresh |
integer, minimum counts to consider a gene "present" in a cell. Default: 0 |
bcds.ntop |
integer, indicating number of top variance genes to consider. Default: 500 |
bcds.srat |
numeric, indicating ratio between orginal number of "cells" and simulated doublets; Default: 1 |
dbf.PCs |
Number of statistically-significant principal components (e.g., as estimated from PC elbow plot); Default: 1:10 |
dbf.pN |
The number of generated artificial doublets, expressed as a proportion of the merged real-artificial data. Default is set to 0.25, based on observation that DoubletFinder performance is largely pN-invariant (see McGinnis, Murrow and Gartner 2019, Cell Systems). |
dbf.pK |
The PC neighborhood size used to compute pANN, expressed as a proportion of the merged real-artificial data. No default is set, as pK should be adjusted for each scRNA-seq dataset. Optimal pK values can be determined using mean-variance-normalized bimodality coefficient. |
chord(seu=NA,doubletrate=NA,k=20,overkill=T,overkillrate=1,outname="out",seed=1)
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