| 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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