| p2app4conos | R Documentation | 
Utility function to generate a pagoda2 app from a conos object
p2app4conos(
  conos,
  cdl = NULL,
  metadata = NULL,
  filename = "conos_app.bin",
  save = TRUE,
  n.cores = 1,
  n.odgenes = 3000,
  nPcs = 100,
  k = 30,
  perplexity = 50,
  log.scale = TRUE,
  trim = 10,
  keep.genes = NULL,
  min.cells.per.gene = 0,
  min.transcripts.per.cell = 100,
  get.largevis = TRUE,
  get.tsne = TRUE,
  make.geneknn = TRUE,
  go.env = NULL,
  cell.subset = NULL,
  max.cells = Inf,
  additional.embeddings = NULL,
  test.pathway.overdispersion = FALSE,
  organism = NULL,
  return.details = FALSE
)
conos | 
 Conos object  | 
cdl | 
 list Optional list of raw matrices (so that gene merging doesn't have to be redone) (default=NULL)  | 
metadata | 
 list Optional list of (named) metadata factors (default=NULL)  | 
filename | 
 string Name of the *.bin file to seralize for the pagoda2 application if save=TRUE (default='conos_app.bin')  | 
save | 
 boolean Save serialized *bin file specified in filename (default=TRUE)  | 
n.cores | 
 integer Number of cores (default=1)  | 
n.odgenes | 
 numeric Number of top overdispersed genes to use (dfault=3e3). From pagoda2::basicP2proc().  | 
nPcs | 
 numeric Number of PCs to use (default=100). From pagoda2::basicP2proc().  | 
k | 
 numeric Default number of neighbors to use in kNN graph (default=30). From pagoda2::basicP2proc().  | 
perplexity | 
 numeric Perplexity to use in generating tSNE and largeVis embeddings (default=50). From pagoda2::basicP2proc().  | 
log.scale | 
 boolean Whether to use log scale normalization (default=TRUE). From pagoda2::basicP2proc().  | 
trim | 
 numeric Number of cells to trim in winsorization (default=10). From pagoda2::basicP2proc().  | 
keep.genes | 
 optional set of genes to keep from being filtered out (even at low counts) (default=NULL). From pagoda2::basicP2proc().  | 
min.cells.per.gene | 
 numeric Minimal number of cells required for gene to be kept (unless listed in keep.genes) (default=0). From pagoda2::basicP2proc().  | 
min.transcripts.per.cell | 
 numeric Minimumal number of molecules/reads for a cell to be admitted (default=100). From pagoda2::basicP2proc().  | 
get.largevis | 
 boolean Whether to caluclate largeVis embedding (default=TRUE). From pagoda2::basicP2proc().  | 
get.tsne | 
 boolean Whether to calculate tSNE embedding (default=TRUE). From pagoda2::basicP2proc().  | 
make.geneknn | 
 boolean Whether pre-calculate gene kNN (for gene search) (default=TRUE). From pagoda2::basicP2proc().  | 
go.env | 
 GO environment for the organism of interest (default=NULL)  | 
cell.subset | 
 string Cells to subset with the conos embedding conos$embedding. If NULL, uses all cells via rownames(conos$embedding) (default=NULL)  | 
max.cells | 
 numeric Limit to the cells that are included in the conos. If Inf, there is no limit (default=Inf)  | 
additional.embeddings | 
 list Additional embeddings to add to conos for the pagoda2 app (default=NULL)  | 
test.pathway.overdispersion | 
 boolean Find all IDs using GO category against either org.Hs.eg.db ('hs') or org.Mm.eg.db ('mm') (default=FALSE  | 
organism | 
 string Organism of interest, either 'hs' (Homo sapiens) or 'mm' (Mus musculus, i.e. mouse) (default=NULL). Only used if test.pathway.overdispersion is TRUE. If NULL and test.pathway.overdispersion=TRUE, then 'hs' is used.  | 
return.details | 
 boolean If TRUE, return list of p2 application, pagoda2 object, list of raw matrices, and cell names. If FALSE, simply return pagoda2 app object. (default=FALSE)  | 
pagoda2 app object
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