Made FastCAR into an actual R package, removed testing and running scripts
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Marijn
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Subproject commit 2121cbd359630af53c002dd3e082621010111346
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###############################################################################
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library(Matrix)
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library(Seurat)
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library(qlcMatrix)
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###############################################################################
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# had to make this function to efficiently modify sparse matrices on a per gene basis
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###############################################################################
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# FastCAR package
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# Marijn Berg
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# m.berg@umcg.nl
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###############################################################################
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# FastCAR removes ambient RNA from 10X data by looking at the profile of the
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# empty droplets and removing per gene the highest value found in the ambient
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# RNA if it's found to contaminate more than a certain threshold of droplets
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###############################################################################
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# This script runs a simple correction with standard settings
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library(Matrix)
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library(Seurat)
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library(qlcMatrix)
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source("R/FastCAR_Base.R")
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emptyDropletCutoff = 100 # Droplets with fewer than this number of UMIs are considered empty
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contaminationChanceCutoff = 0.05 # This is the maximum fraction of droplets containing the contamination
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cellExpressionFolder = c("/home/marijn/Analysis_Drive/R_Projects/scRNA_Background_correction/Cellranger_output/4951STDY7487591_ARMS054/filtered_feature_bc_matrix/")
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fullMatrixFolder = c("/home/marijn/Analysis_Drive/R_Projects/scRNA_Background_correction/Cellranger_output/4951STDY7487591_ARMS054/raw_feature_bc_matrix/")
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# This folder will contain the corrected cell matrix
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correctedMatrixFolder = c("/home/marijn/Analysis_Drive/R_Projects/scRNA_Background_correction/Cellranger_output/4951STDY7487591_ARMS054/corrected_feature_bc_matrix")
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# these are literally wrappers for the Seurat functions but it's good practice in case the function changes later
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cellMatrix = read.cell.matrix(cellExpressionFolder)
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fullMatrix = read.full.matrix(fullMatrixFolder)
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###############################################################################
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# This is an optional function that will show the effects of different cutoff values
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# start, stop, and by all refer to number of UMI, it determines the background ate steps of by, from start to stop
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ambProfile = describe.ambient.RNA.sequence(fullCellMatrix = fullMatrix, start = 10, stop = 500, by = 10, contaminationChanceCutoff = 0.05)
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plot.ambient.profile(ambProfile)
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###############################################################################
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ambientProfile = determine.background.to.remove(fullMatrix, cellMatrix, emptyDropletCutoff, contaminationChanceCutoff)
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cellMatrix = remove.background(cellMatrix, ambientProfile)
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write.corrected.matrix(cellMatrix, correctedMatrixFolder, ambientProfile)
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###############################################################################
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# FastCAR package
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# Marijn Berg
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# m.berg@umcg.nl
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###############################################################################
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# FastCAR removes ambient RNA from 10X data by looking at the profile of the
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# empty droplets and removing per gene the highest value found in the ambient
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# RNA if it's found to contaminate more than a certain threshold of droplets
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###############################################################################
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# This script contains functions to profile the Ambient RNA to suggest
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# good settings to use to find genes to correct for
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###############################################################################
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library(Matrix)
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library(Seurat)
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library(qlcMatrix)
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###############################################################################
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# describe the number of genes identified in the background
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# and the number of genes failing the contaminiation chance threshold
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#
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describe.ambient.RNA.sequence = function(fullCellMatrix, start, stop, by, contaminationChanceCutoff){
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genesInBackground = vector(mode = "numeric", length = length(seq(start, stop, by)))
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genesContaminating = vector(mode = "numeric", length = length(seq(start, stop, by)))
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nEmptyDroplets = vector(mode = "numeric", length = length(seq(start, stop, by)))
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ambientDescriptions = data.frame(nEmptyDroplets, genesInBackground, genesContaminating)
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rownames(ambientDescriptions) = seq(start, stop, by)
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for(emptyCutoff in seq(start, stop, by)){
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nEmpty = table((Matrix::colSums(fullCellMatrix) < emptyCutoff) &(Matrix::colSums(fullCellMatrix) > 0))[2]
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occurences = rowSums(fullCellMatrix[,Matrix::colSums(fullCellMatrix) < emptyCutoff] !=0)
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#probability of a background read of a gene ending up in a cell
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probabiltyCellContaminationPerGene = occurences / nEmpty
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nFailingThreshold = sum(probabiltyCellContaminationPerGene > contaminationChanceCutoff)
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nGenes = sum(occurences != 0)
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ambientDescriptions[as.character(emptyCutoff), c(1,2,3)] = c(nEmpty ,nGenes, nFailingThreshold)
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}
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return(ambientDescriptions)
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}
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plot.ambient.profile = function(ambientProfile){
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par(mfrow = c(3,1))
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plot(as.numeric(rownames(ambientProfile)), ambientProfile[,1],
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main = "Total number of empty droplets at cutoffs",
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xlab = "empty droplet UMI cutoff",
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ylab = "Number of empty droplets")
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plot(as.numeric(rownames(ambientProfile)), ambientProfile[,2],
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main = "Number of genes in ambient RNA",
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xlab = "empty droplet UMI cutoff",
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ylab = "Genes in empty droplets")
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plot(as.numeric(rownames(ambientProfile)), ambientProfile[,3],
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main = "number of genes to correct",
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xlab = "empty droplet UMI cutoff",
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ylab = "Genes identified as contamination")
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}
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102
R/tmp.R
102
R/tmp.R
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cutoffEmpty = 100 # set this to NA to determine dynamicallly
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###############################################################################
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# remove this or things will keep getting added to it
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rm(biopsySeurat, backGroundOverviews)
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for(folder in dataFolders[1]){
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gc()
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donor = str_sub(folder, -7,-1)
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sample = str_sub(folder, 19)
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sample = str_sub(sample, 1, -9)
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allExpression = Read10X(paste(folder, "/raw_feature_bc_matrix", sep = ""))
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colnames(allExpression) = paste(datasetInfo[sample, "prefix"], colnames(allExpression), sep = "")
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# change barcode ids to match r object
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if(is.na(cutoffEmpty)){
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##########################################
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# determine the number of genes in the empty droplets at various cutoffs
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foundNumberOfGenes = vector(mode = "numeric", length = length(seq(kneePointStart, kneePointStop, kneePointSteps)))
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names(foundNumberOfGenes) = as.character(seq(kneePointStart, kneePointStop, kneePointSteps))
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for(cutoffValue in seq(kneePointStart, kneePointStop, kneePointSteps)){
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nExpressedCells = Matrix::rowSums(allExpression[, Matrix::colSums(allExpression) < cutoffValue])
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nExpressedCells[nExpressedCells > 0] = 1
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foundNumberOfGenes[as.character(cutoffValue)]= sum(nExpressedCells)
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}
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write.table(foundNumberOfGenes, file = paste("Foundgenes_cutoff_", donor, ".csv"))
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##########################################
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# Find the point where increase in the number of genes decreases the most
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cutoffEmpty = which(diff(foundNumberOfGenes) == max(diff(foundNumberOfGenes)[find_peaks(diff(foundNumberOfGenes))]))
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# cutoffEmpty = as.numeric(names(which(diff(foundNumberOfGenes) == min(diff(foundNumberOfGenes)))))[1] # have to add this at the end, multiple changes can be the same value
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##########################################
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png(paste("Empty_droplets_content_", donor, ".png", sep = ""), height = 400, width = 800)
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plot(as.numeric(names(foundNumberOfGenes)), foundNumberOfGenes, main = paste(donor, " unique genes per cutoff"), xlab = "cutoff <")
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segments(cutoffEmpty, 0 ,cutoffEmpty, 25000)
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dev.off()
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}
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# read this in as a full matrix, haven't figgered out how to do this on a sparse matrix
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cellExpression = allExpression[,cellIDs[cellIDs %in% colnames(allExpression)]]
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if(!exists("biopsySeurat")){
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biopsySeurat <<- CreateSeuratObject(cellExpression, project = "Bronchial_Biopsy")
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biopsySeurat[["orig.ident"]] = donor
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biopsySeurat[["percent.mt"]] <- PercentageFeatureSet(biopsySeurat, pattern = "^MT-")
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# biopsySeurat <- subset(biopsySeurat, subset = percent.mt < quantile(biopsySeurat@meta.data$percent.mt, c(.9)) )
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}else{
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tmpbiopsySeurat = CreateSeuratObject(cellExpression, project = "Bronchial_Biopsy")
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tmpbiopsySeurat[["orig.ident"]] = donor
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tmpbiopsySeurat[["percent.mt"]] <- PercentageFeatureSet(tmpbiopsySeurat, pattern = "^MT-")
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# tmpbiopsySeurat <- subset(tmpbiopsySeurat, subset = percent.mt < quantile(tmpbiopsySeurat@meta.data$percent.mt, c(.9), na.rm = TRUE))
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biopsySeurat = merge(biopsySeurat, tmpbiopsySeurat)
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}
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backgroundTotal = Matrix::rowSums(allExpression[,Matrix::colSums(allExpression) < cutoffEmpty])
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backGroundMax = as.vector(rowMax(allExpression[names(backgroundTotal),Matrix::colSums(allExpression) < cutoffEmpty]))
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nCell = ncol(cellExpression)
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# droplets that are empty but not unused barcodes, unused barcodes have zero reads assigned to them.
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nEmpty = table((Matrix::colSums(allExpression) < cutoffEmpty) &(Matrix::colSums(allExpression) > 0))[2]
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occurences = rowSums(allExpression[,Matrix::colSums(allExpression) < cutoffEmpty] !=0)
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#probability of a background read of a gene ending up in a cell
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pCell = occurences / nEmpty
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write.csv(pCell, file = paste("pCell_", donor, ".csv", sep = ""))
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write.csv(backGroundMax, file = paste("bgMax_", donor, ".csv", sep = ""))
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# set the background value for those genes that are unlikely to be a significant contaminant to 0 (zero)
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backGroundMax[pCell < acceptableFractionContaminated] = 0
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# remove the background
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cellExpression = apply(cellExpression , 2, '-', backGroundMax)
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cellExpression[cellExpression < 0] = 0
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# cellExpression = as.sparse(cellExpression)
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if(!exists("biopsySeuratAC")){
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biopsySeuratAC <<- CreateSeuratObject(cellExpression, project = "AC_Bronchial_Biopsy")
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biopsySeuratAC[["orig.ident"]] = donor
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biopsySeuratAC[["percent.mt"]] <- PercentageFeatureSet(biopsySeuratAC, pattern = "^MT-")
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# biopsySeuratAC <- subset(biopsySeuratAC, subset = percent.mt < quantile(biopsySeuratAC@meta.data$percent.mt, c(.9)) )
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}else{
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tmpbiopsySeuratAC = CreateSeuratObject(cellExpression, project = "AC_Bronchial_Biopsy")
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tmpbiopsySeuratAC[["orig.ident"]] = donor
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tmpbiopsySeuratAC[["percent.mt"]] <- PercentageFeatureSet(tmpbiopsySeuratAC, pattern = "^MT-")
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# tmpbiopsySeuratAC <- subset(tmpbiopsySeuratAC, subset = percent.mt < quantile(tmpbiopsySeuratAC@meta.data$percent.mt, c(.9), na.rm = TRUE))
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biopsySeuratAC = merge(biopsySeuratAC, tmpbiopsySeuratAC)
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}
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}
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