Description Usage Arguments Value Examples
This function plot basic clustering result for seurat object
1 2 3 4 5 6 7 | Fullplot_v2(object, name, topgene = NULL, resolusion = "res.0.6",
signiture = c("INS", "GCG", "SST", "PPY", "KRT19", "COL1A2", "REG1A",
"DNAJB1", "GHRL"), p.tsnecluster = T, Pheatmap = T,
p.tsnesample = T, p.pcacluster = T, p.pcasample = T,
darwPCdrive = T, cell.use = 500, color = "Paired", PC34 = F,
dotsize = 0.1, heatmapannosize = 0.5, doreturn = F, pdfwidth = 7,
pdfheight = 7)
|
object |
The seurat object that has been analyzed. |
name |
the name for pdf file |
topgene |
An optional input of cluster marker genes if "Gettopgenes" has been run outside. This can help to save some time |
resolusion |
This is clustering resolution used in clustering, which can be found in object@data.info |
signiture |
a vector of gene names that are intersting to be checked on tsne by color intensity |
p.tsnecluster |
if true, plot the tsne figure stained by clusters |
Pheatmap |
if true, plot the marker gene heatmap |
p.tsnesample |
if true, plot the tsne figure stained by samples |
p.pcacluster |
if true, plot the pca12 figure stained by clusters |
p.pcasample |
if true, plot the pca12 figure stained by sample |
darwPCdrive |
if true, plot the heatmap showing the pca driving genes |
cell.use |
the cell number used to draw PCA driving gene plot. Default is 500 |
color |
The color palette used for tsne and pca, default is "Paired" |
PC34 |
If ture, also plot PCA34 additionally, default is FALSE |
dotsize |
The dot size for tsne and pca |
doreturn |
If ture, retun plot to a variable |
pdfwidth |
The width of pdf file. Default is 7 |
pdfheight |
The height of pdf file. Default is 7 |
generate a pdf, if doreturn=T then return the figures
1 | Fullplot_v2(S7rock_1.ob,"S7rock_1.ob.pdf",topgene=NULL,resolusion="res.0.6",signiture=c("INS","GCG","SST","PPY","KRT19","COL1A2","REG1A","DNAJB1","GHRL"))
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.