Fast embedding and visualization of multidimensional datasets, originally intended for flow/mass cytometry data. Compatible with FlowSOM (https://github.com/SofieVG/FlowSOM).
You may read more about EmbedSOM in the research paper here:
Miroslav Kratochvíl, Abhishek Koladiya, and Jiří Vondrášek. "Generalized EmbedSOM on quadtree-structured self-organizing maps" F1000Research 8 (2019). doi:10.12688/f1000research.21642.2
Use devtools:
devtools::install_github('exaexa/EmbedSOM')EmbedSOM works by aligning the points to a precomputed self-organizing map (SOM). The main function EmbedSOM takes the SOM and data, and returns a matrix with 2D point coordinates on each row.
Quick way to get a visualization of multidimensional points saved in rows of d:
map <- EmbedSOM::SOM(d, xdim=20, ydim=20) # compute the self-organizing map
e <- EmbedSOM::EmbedSOM(d, map) # compute 2D coordinates of points
EmbedSOM::PlotEmbed(e) # plot the result with densityThere are some parameters that affect speed, precision and shape of the embedding. Use ?EmbedSOM::EmbedSOM to explore them in the documentation.
To get started quickly, you can have a look at the vignettes:
- Basic embedding on a toy dataset
- Visualization of single-cell cytometry data from A FCS file
- Advanced visualization of cytometry data with pseudotime
- Embedding 3D animal skeleton pointclouds to 2D
Use flowCore functionality to add any information to a FCS. The following template saves the scaled FlowSOM object data as-is, together with the embedding:
fs <- FlowSOM::ReadInput('original.fcs', scale=T, ...)
fs <- FlowSOM::BuildSOM(fs, ...)
e <- EmbedSOM::EmbedSOM(fs, ...)
flowCore::write.FCS(new('flowFrame',
exprs=as.matrix(data.frame(fs$data,
embedsom1=e[,1],
embedsom2=e[,2]))),
'original_with_embedding.fcs')See flowCore documentation for information about advanced FCS-writing functionality, e.g. for column descriptions.
Train a SOM on an aggregate file, and use it to embed the individual files. It is important to always apply the same scaling and transformations on all input files.
fs <- FlowSOM::ReadInput(
FlowSOM::AggregateFlowFrames(c('file1.fcs', 'file2.fcs', ...),
cTotal=100000),
scale=T, transform=...)
n <- length(fs$scaled.scale)-2
map <- FlowSOM::SOM(fs)
fs1 <- FlowSOM::ReadInput('file1.fcs',
scale=T,
scaled.scale=fs$scaled.scale[1:n],
scaled.center=fs$scaled.center[1:n],
transform=...)
e1 <- EmbedSOM::EmbedSOM(fs1, map=map)
EmbedSOM::PlotEmbed(e1, fsom=fs1)
# repeat as needed for file2.fcs, etc.See documentation in ?PlotEmbed. By default, PlotEmbed plots a simple colored representation of point density. If supplied with a FCS column name (or number), it uses the a color scale similar to ColorBrewer's RdYlBu (with improvements for transparent stuff) to plot a single marker expression. Parameters red, green and blue can be used to set column names (or numbers) to mix RGB color from marker expressions.
PlotEmbed optionally accepts parameter col with a vector of R colors, which, if provided, is just forwarded to the internal plot function. For example, use col=rgb(0,0,0,0.2) for transparent black points.
New! if you need to mix more nicer colors than just the default RGB, use ExprColors.
Use scattermore: https://github.com/exaexa/scattermore
A pretty fast (and still precise) way to dissect the dataset is to run a metaclustering on SOM clusters, and map the result to the individual points:
clusters <- cutree(k=10, hclust(method='average', dist(map$codes)))[map$mapping[,1]]After that, the metaclusters can be plotted in the embedding. Because the clustering is related to the small SOM-defined "pre-clusters" rather than the individual points, it is necessary to map the individual points to these clusters first:
EmbedSOM::PlotEmbed(e, clust=clusters)After you choose a metacluster in the embedding, use the color scale to find its number, then filter the points in your dataset to the corresponding subset. This example selects the point subset in metacluster number 5 and 6:
d <- d[clusters %in% c(5,6), ]There is now support for 3D SOM grids and 3D embedding. You need the customized SOM function from EmbedSOM:
map <- EmbedSOM::SOM(someData, xdim=8, ydim=8, zdim=8)
e <- EmbedSOM::EmbedSOM(data=someData, map=map)PlotEmbed and other functions do not work on 3D points in embed, but you may use other libraries to display the plots. For example, the plot3D library:
plot3D::scatter3D(x=e[,1], y=e[,2], z=e[,3])Interactive rotatable and zoomable plots are provided by the rgl library:
rgl::points3d(x=e[,1], y=e[,2], z=e[,3])You may use parallelized versions of the algorithms. Several functions (SOM, GQTSOM, EmbedSOM) support setting parallel=T, which enables parallel processing; you may fine-tune the number of used CPUs by setting e.g. threads=5.
For SOM training, you need to explicitly switch to the parallelizable batch version, using batch=T, parallel=T.
Additionally, EmbedSOM has support for SIMD-assisted computation of both SOM and the embedding. If your CPU can work with SSE4 instructions (almost every amd64 (a.k.a. x64 a.k.a. x86_64) CPU built after around 2013 can do that), just tell R to compile your code with correct C++ flags, and SOM+EmbedSOM computation should get faster! (the usual speedup is at least around 3x, depending on the CPU and dataset shape)
First, add a correct line to the R Makevars config file:
$ cat ~/.R/Makevars
CXXFLAGS += -O3 -march=nativeAfter reinstalling EmbedSOM, SIMD code will be used by default. Note that only the functions from EmbedSOM are affected, i.e. you will need to use EmbedSOM::SOM instead of FlowSOM::SOM and BuildSOM to get this speedup.