I would like to analyze a published scRNAseq dataset by making a new Seurat Object. The authors have published their tSNE.1 and tSNE.2 coordinates in addition to all of their metadata but I cannot find how to create a tSNE reduction using their tSNE coordinates.
I'm assuming that I still do basic pre-processing, runPCA and runTSNE but any information on how to project the provided embeddings would be greatly appreciated.
library(dplyr)
library(Seurat)
library(patchwork)
library(ggplot2)
library(data.table)
library(magrittr)
library(Matrix)
data_dir <- 'path/to/data/'
list.files(data_dir)
expression_matrix <- Read10X(data.dir = data_dir)
fish_LD = CreateSeuratObject(counts = expression_matrix)
metadata <- read.csv('meta.csv') # dataframe I created from barcodes.tsv.gz
Sample <- metadata[1]
Cell.type<- metadata[2]
tSNE.1 <- metadata[3]
tSNE.2 <- metadata[4]
nGene <- metadata[5]
nUMI <- metadata[6]
Percentage.of.mitochondrial.genes <- metadata[7]
Percentage.of.ribosomal.protein.genes <- metadata[8]
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(Sample = Sample,
row.names = rownames(fish_LD@meta.data)))
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(Cell.type = Cell.type, row.names = rownames(fish_LD@meta.data)))
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(tSNE.1 = tSNE.1, row.names = rownames(fish_LD@meta.data)))
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(tSNE.2 = tSNE.2, row.names = rownames(fish_LD@meta.data)))
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(nGene = nGene, row.names = rownames(fish_LD@meta.data)))
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(nUMI = nUMI, row.names = rownames(fish_LD@meta.data)))
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(Percentage.of.mitochondrial.genes = Percentage.of.mitochondrial.genes, row.names = rownames(fish_LD@meta.data)))
fish_LD <- AddMetaData(object = fish_LD, metadata = data.frame(Percentage.of.mitochondrial.genes = Percentage.of.mitochondrial.genes, row.names = rownames(fish_LD@meta.data)))
Thank you, that was extremely helpful and fully recapitulates the original graph. I suppose what I'm trying to do is use seurat functionality (ie. FeaturePlot) but with these tSNE.1 and tSNE.2 coordinates. Any suggestions on how I might accomplish that?
straightforward: add the gene expression as a column in the metadata and change color=Cell.type to color=yourcolumn
there might be some way to do the feature plot normally but i would have to play around with it. you might be able to set dim.1 and dim.2 to fish_LD@meta.data$tSNE.1 etc...