dsb

This package was developed at John Tsang’s Lab by Matt Mulè and Andrew Martins. The package implements our normalization and denoising method for CITEseq data. Technical discussion of how the method works can be found in the biorxiv preprint We utilized the dsb package to normalize CITEseq data reported in this paper

In the biorxiv preprint, comparing unstained control cells and empty droplets we found the major contribotor to background noise in CITEseq data is unbound antibody captured and sequenced in droplets. DSB corrects for this background by leveraging empty droplets which serve as a “built in” noise measurement in any droplet capture single cell platform (e.g. 10X, dropseq, indrop).

In addition we define a per-cell denoising covariate to account for the technical component of library size differences between cells which removes spurious cluster formation derived from globally dimcells clustering together.

installation

You can install the released version of dsb in your R session with the command below

# this is analagous to install.packages("package), you need the package devtools to install a package from a github repository like this one. 
require(devtools)
#> Loading required package: devtools
#devtools::install_github(repo = 'MattPM/dsb')

quickstart

# load package and normalize the example raw data 
library(dsb)


# normalize
normalized_matrix = DSBNormalizeProtein(cell_protein_matrix = cells_citeseq_mtx,
                                        empty_drop_matrix = empty_drop_citeseq_mtx)

The full version (recommended)

By default dsb defines the per cell denoising covariate by fitting a gaussian mixture model to the log + 10 counts of each cell and defining the noise ocvariates the mean. We reccomend including the counts from isotype controls in each cell in the denoising covariates.

# get the empty cells from demultiplexing with 


# define a vector of the isotype controls in the data 
isotypes = c("Mouse IgG2bkIsotype_PROT", "MouseIgG1kappaisotype_PROT","MouseIgG2akappaisotype_PROT", "RatIgG2bkIsotype_PROT")

normalized_matrix = DSBNormalizeProtein(cell_protein_matrix = cells_citeseq_mtx,
                                        empty_drop_matrix = empty_drop_citeseq_mtx,
                                        use.isotype.control = TRUE,
                                        isotype.control.name.vec = isotypes)

visualize distributions of CD4 and CD8

plot raw points (overplotted) and points with labeled density distributions (similar to flow)

# plot this and avoid plotting by adding a density gradient like a flowjo plot
# this nice density function is from here: https://slowkow.com/notes/ggplot2-color-by-density/
get_density = function(x, y, ...) {
  dens <- MASS::kde2d(x, y, ...)
  ix <- findInterval(x, dens$x)
  iy <- findInterval(y, dens$y)
  ii <- cbind(ix, iy)
  return(dens$z[ii])
}

library(ggplot2)
data.plot = normalized_matrix %>% t %>%
  as.data.frame() %>% 
  dplyr::select(CD4_PROT, CD8_PROT) 
data.plot = data.plot %>%   dplyr::mutate(density = get_density(data.plot$CD4_PROT, data.plot$CD8_PROT, n = 100)) 

# plot with and without density gradient
p1 = ggplot(data.plot, aes(x = CD8_PROT, y = CD4_PROT, color = density)) +
  geom_point(size = 0.4) +
  geom_vline(xintercept = 0, color = "red", linetype = 2) + 
  geom_hline(yintercept = 0, color = "red", linetype = 2) + 
  viridis::scale_color_viridis(option = "B") +  
  scale_shape_identity() 
p2 = ggplot(data.plot, aes(x = CD8_PROT, y = CD4_PROT)) +
  geom_point(size = 0.4) +
  geom_vline(xintercept = 0, color = "red", linetype = 2) + 
  geom_hline(yintercept = 0, color = "red", linetype = 2) 

cowplot::plot_grid(p1,p2)

The plots above show the actual protein distributions. There is no artificial jitter added to points.

#How do I get the empty droplets?

there are a number of ways to get the empty drops. If you are using cell hashing, when you demultiplex the cells, you get a vector of empty or Negative droplets.

HTODemux function in Seurat: https://satijalab.org/seurat/v3.1/hashing_vignette.html

deMULTIplex function from Multiseq (this is now also implemented in Seurat). https://github.com/chris-mcginnis-ucsf/MULTI-seq

If you’re not multiplexing you can simply get a vector of negative droplets from the cells you would remove. https://genomebiology.biomedcentral.com/articles/10.1186/s13059-019-1662-y

Simple example workflow (Seurat Version 3)

# get the ADT counts using Seurat version 3 
seurat_object = HTODemux(seurat_object, assay = "HTO", positive.quantile = 0.99)
Idents(seurat_object) = "HTO_classification.global"
neg_object = subset(seurat_object, idents = "Negative")
singlet_object = subset(seurat_object, idents = "Singlet")


# non sparse CITEseq data actually store better in a regular materix so the as.matrix() call is not memory intensive.
neg_adt_matrix = GetAssayData(neg_object, assay = "CITE", slot = 'raw.data') %>% as.matrix()
positive_adt_matrix = GetAssayData(singlet_object, assay = "CITE", slot = 'raw.data') %>% as.matrix()


# normalize the data with dsb
# make sure you've run devtools::install_github(repo = 'MattPM/dsb')
normalized_matrix = DSBNormalizeProtein(cell_protein_matrix = positive_adt_matrix,
                                        empty_drop_matrix = neg_adt_matrix)


# now add the normalized dat back to the object (the singlets defined above as "object")
singlet_object = SetAssayData(object = singlet_object, slot = "CITE", new.data = normalized_matrix)

In reality you might want to confirm the cells called as “Negative” have low RNA / gene content to be certain there are no contaminating cells.

Also it is not necessary but we reccomend demultiplexing with teh raw output from cellranger rather than the processed output because the raw (i.e. outs/raw_feature_bc_matrix) will have more empty droplets from which the HTODemux function will be able to estimate the negative population = it is not required but in general these functions perform better with more negative droplets. This will also have the advantage of creating more droplets to use as built protein background controls in the DSB function.

example workflow Seurat version 2

# get the ADT counts using Seurat version 3 
seurat_object = HTODemux(seurat_object, assay = "HTO", positive.quantile = 0.99)

neg = seurat_object %>%
  SetAllIdent(id = "hto_classification_global") %>% 
  SubsetData(ident.use = "Negative") 

singlet = seurat_object %>%
  SetAllIdent(id = "hto_classification_global") %>% 
  SubsetData(ident.use = "Singlet") 

# get negative and positive ADT data 
neg_adt_matrix = neg@assay$CITE@raw.data %>% as.matrix()
pos_adt_matrix = singlet@assay$CITE@raw.data %>% as.matrix()


# normalize the data with dsb
# make sure you've run devtools::install_github(repo = 'MattPM/dsb')
normalized_matrix = DSBNormalizeProtein(cell_protein_matrix = pos_adt_matrix,
                                        empty_drop_matrix = neg_adt_matrix)


# add the assay to the Seurat object 
singlet = SetAssayData(object = singlet, slot = "CITE", new.data = normalized_matrix)

Get empty drops if you’re not sample multiplexing

you can simply get a vector of negative droplets from the cells you would remove. There are also more robust ways to detect empty droplets https://genomebiology.biomedcentral.com/articles/10.1186/s13059-019-1662-y

here is a crude way to get some likely empty droplets assuming seurat_object is a object with most cells (i.e. any cell expressing at least a gene)

# get the nUMI from a seurat version 3 object 
umi = seurat_object$nUMI

#  Get the nUMI from a Seurat version 2 objec 
umi = seurat_object@meta.data %>% select("nUMI")
mu_umi = mean(umi)
sd_umi = sd(umi)

# calculate a threshold for calling a cell negative 
sub_threshold = mu_umi - (2*sd_umi)



Idents(seurat_object) = "nUMI"


# this negative cell object can be used to define the negative background following the examples above. 
neg = subset(seurat_object, accept.high = sub_threshold)