nnSVG is a method for scalable identification of spatially variable genes (SVGs) in spatially-resolved transcriptomics data.
The nnSVG method is based on nearest-neighbor Gaussian processes (Datta et al., 2016, Finley et al., 2019) and uses the BRISC algorithm (Saha and Datta, 2018) for model fitting and parameter estimation. nnSVG allows identification and ranking of SVGs with flexible length scales across a tissue slide or within spatial domains defined by covariates. The method scales linearly with the number of spatial locations and can be applied to datasets containing thousands or more spatial locations.
nnSVG is implemented as an R package within the Bioconductor framework, and is available from Bioconductor.
Our paper describing the method is available from Nature Communications.
The package can be installed from Bioconductor as follows, using R version 4.2 or above:
install.packages("BiocManager")
BiocManager::install("nnSVG")Alternatively, the latest development version of the package can also be installed from GitHub:
remotes::install_github("lmweber/nnSVG")If you are installing from GitHub, the following dependency packages may need to be installed manually from Bioconductor and CRAN (these are installed automatically if you install from Bioconductor instead):
install.packages("BiocManager")
BiocManager::install("SpatialExperiment")
BiocManager::install("STexampleData")
install.packages("BRISC")A detailed tutorial is available in the package vignette from Bioconductor. A direct link to the tutorial / package vignette is available here.
In the examples below, we assume the input data are provided as a SpatialExperiment Bioconductor object. In this case, the outputs are stored in the rowData of the SpatialExperiment object.
Alternatively, the inputs can also be provided as a numeric matrix of normalized and transformed counts (e.g. log-transformed normalized counts, also known as logcounts) and a numeric matrix of spatial coordinates.
A short example workflow is shown below. This is a modified version of the full tutorial available in the package vignette from Bioconductor. A direct link to the tutorial / package vignette is available here).
Load packages
library(nnSVG)
library(STexampleData)
library(scran)
library(ggplot2)Load example dataset
# load example dataset from STexampleData package
spe <- Visium_humanDLPFC()
dim(spe)## [1] 33538 4992Preprocessing
# keep spots over tissue
spe <- spe[, colData(spe)$in_tissue == 1]
dim(spe)## [1] 33538 3639# spot-level quality control: already performed on this example dataset# filter low-expressed and mitochondrial genes
# using function from nnSVG package with default filtering parameters
spe <- filter_genes(spe)## Gene filtering: removing mitochondrial genes
## removed 13 mitochondrial genes
## Gene filtering: retaining genes with at least 3 counts in at least 0.5% (n = 19) of spatial locations
## removed 30216 out of 33525 genes due to low expression# calculate logcounts (log-transformed normalized counts) using scran package
# using library size factors
spe <- computeLibraryFactors(spe)
spe <- logNormCounts(spe)
assayNames(spe)## [1] "counts" "logcounts"Subset data for this example
# select small set of random genes and several known SVGs for faster runtime in this example workflow
set.seed(123)
ix_random <- sample(seq_len(nrow(spe)), 10)
known_genes <- c("MOBP", "PCP4", "SNAP25", "HBB", "IGKC", "NPY")
ix_known <- which(rowData(spe)$gene_name %in% known_genes)
ix <- c(ix_known, ix_random)
spe <- spe[ix, ]
dim(spe)## [1] 16 3639Run nnSVG
# set seed for reproducibility
# run nnSVG using a single thread for this example workflow
set.seed(123)
spe <- nnSVG(spe, n_threads = 1)
# show results
rowData(spe)## DataFrame with 16 rows and 17 columns
## [...]Investigate results
The results are stored in the rowData of the SpatialExperiment object.
The main results of interest are:
LR_stat: likelihood ratio (LR) statistics used to rank SVGsrank: rank of top SVGs according to LR statisticspval: approximate p-valuespadj: approximate p-values adjusted for multiple testingprop_sv: effect size defined as proportion of spatial variance
# number of significant SVGs
table(rowData(spe)$padj <= 0.05)##
## FALSE TRUE
## 7 9# show results for top n SVGs
n <- 10
rowData(spe)[order(rowData(spe)$rank)[1:n], ]## DataFrame with 10 rows and 17 columns
## gene_id gene_name feature_type sigma.sq tau.sq
## <character> <character> <character> <numeric> <numeric>
## ENSG00000168314 ENSG00000168314 MOBP Gene Expression 1.38739383 0.364188
## ENSG00000132639 ENSG00000132639 SNAP25 Gene Expression 0.43003959 0.430106
## ENSG00000211592 ENSG00000211592 IGKC Gene Expression 0.56564845 0.455042
## ENSG00000244734 ENSG00000244734 HBB Gene Expression 0.32942113 0.353754
## ENSG00000183036 ENSG00000183036 PCP4 Gene Expression 0.23102220 0.452735
## ENSG00000122585 ENSG00000122585 NPY Gene Expression 0.28567359 0.280173
## ENSG00000129562 ENSG00000129562 DAD1 Gene Expression 0.02389607 0.464723
## ENSG00000114923 ENSG00000114923 SLC4A3 Gene Expression 0.01147170 0.237260
## ENSG00000133606 ENSG00000133606 MKRN1 Gene Expression 0.00632248 0.272432
## ENSG00000143543 ENSG00000143543 JTB Gene Expression 0.07541566 0.463623
## phi loglik runtime mean var spcov
## <numeric> <numeric> <numeric> <numeric> <numeric> <numeric>
## ENSG00000168314 1.102018 -3663.60 0.631 0.805525 1.205673 1.462248
## ENSG00000132639 3.033847 -3912.70 0.450 3.451926 0.857922 0.189973
## ENSG00000211592 20.107022 -4531.64 1.054 0.622937 1.007454 1.207340
## ENSG00000244734 27.814098 -4044.96 1.559 0.411262 0.697673 1.395587
## ENSG00000183036 8.272278 -4026.22 0.419 0.687961 0.684598 0.698656
## ENSG00000122585 71.653290 -3995.23 0.843 0.393975 0.567383 1.356646
## ENSG00000129562 10.141894 -3842.24 0.590 0.549318 0.489167 0.281410
## ENSG00000114923 12.765645 -2617.36 0.658 0.250768 0.248816 0.427112
## ENSG00000133606 0.082764 -2831.51 0.612 0.295404 0.278806 0.269171
## ENSG00000143543 119.721419 -4036.28 0.731 0.654919 0.539172 0.419318
## prop_sv loglik_lm LR_stat rank pval padj
## <numeric> <numeric> <numeric> <numeric> <numeric> <numeric>
## ENSG00000168314 0.7920804 -5503.33 3679.46397 1 0.00000e+00 0.00000e+00
## ENSG00000132639 0.4999614 -4884.19 1942.98556 2 0.00000e+00 0.00000e+00
## ENSG00000211592 0.5541822 -5176.53 1289.77508 3 0.00000e+00 0.00000e+00
## ENSG00000244734 0.4821910 -4507.99 926.04573 4 0.00000e+00 0.00000e+00
## ENSG00000183036 0.3378716 -4473.57 894.68884 5 0.00000e+00 0.00000e+00
## ENSG00000122585 0.5048609 -4131.87 273.27818 6 0.00000e+00 0.00000e+00
## ENSG00000129562 0.0489053 -3861.98 39.49098 7 2.65854e-09 6.07667e-09
## ENSG00000114923 0.0461207 -2632.02 29.31376 8 4.31119e-07 8.62238e-07
## ENSG00000133606 0.0226812 -2839.08 15.15227 9 5.12539e-04 9.11181e-04
## ENSG00000143543 0.1399077 -4039.07 5.59664 10 6.09124e-02 9.74599e-02Plot expression of top SVG
Plot expression of the top-ranked SVG.
# plot spatial expression of top-ranked SVG
ix <- which(rowData(spe)$rank == 1)
ix_name <- rowData(spe)$gene_name[ix]
ix_name## [1] "MOBP"df <- as.data.frame(cbind(spatialCoords(spe), expr = counts(spe)[ix, ]))
ggplot(df, aes(x = pxl_col_in_fullres, y = pxl_row_in_fullres,
color = expr)) +
geom_point(size = 0.8) +
coord_fixed() +
scale_y_reverse() +
scale_color_gradient(low = "gray90", high = "blue",
trans = "sqrt", breaks = range(df$expr),
name = "counts") +
ggtitle(ix_name) +
theme_bw() +
theme(plot.title = element_text(face = "italic"),
panel.grid = element_blank(),
axis.title = element_blank(),
axis.text = element_blank(),
axis.ticks = element_blank())
Our paper describing nnSVG is available from Nature Communications: