knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "README-" )
The goal of boclust is to provide a new normalization method for sparse data by a feature boosting strategy with the latent representation, especially for scRNA-seq data consisted of many zeros. Based on the normalization, a new measure of similarity is defined for the following clustering algorithm. Unlike other unsupervised cluster methods, boclust provides the suggestion K to determine the number of clusters. In this way, it may be unsuitable for low-dimentional data.
There are three major functions:
You can install boclust from github with:
# install.packages("devtools") devtools::install_github("TinyOpen/boclust")
sparse.data <- data.frame(g.1 = c(0, 5, 0, 6, 8, 6, 7, 7), g.2 = c(5, 0, 0, 0, 5, 7, 5, 7)) # generate sparse data from the toy model of CIDR bossa.change <- BossaSimi(sparse.data, is.pca = FALSE) # with low-dimensional data, pca is uncessary data.after <- bossa.change$U.score.non.pca # data after normalization
You can check after normalization, the first 4 cells which are actually from the same cluster are more closer. The seperation between the first 4 cells and the last 4 cells is large enough to get the correct clustering result.
d3heatmap(sparse.data) ## show heatmap of original data d3heatmap(data.after) ## show heatmap of bossa-normalized data
Now, when it comes to your high-dimentional data, which is the target which boclust
is designed for. You can either use BossaClust
to get the final result:
object <- BossaClust(high.dim.data) # do normalization and clustering at the same time bossa_interactive(object) # use shiny frame to show the result
Or, you can store the normalized data first, which is obtained from function BossaSimi
, and then do the rest work.
pre.object <- BossaSimi(high.dim.data) object <- BossaClust(data = high.dim.data, data.pre = pre.object) # do normalization and clustering at the same time bossa_interactive(object) # use shiny frame to show the result
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