knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "man/figures/README-", out.width = "100%" )
SCIBER is a simple method that outputs the batch-effect corrected expression data in the original space/dimension. These expression data of individual genes can be directly used for all follow-up analyses. SCIBER has four steps; each step has a clear biological meaning, and the algorithms used for them are k-means clustering, t-test, Fisher’s exact test, and linear regression, respectively, all of which are easily comprehensible
You can install the development version of SCIBER with the following instructions:
# install.packages("devtools") devtools::install_github("RavenGan/SCIBER")
The following example uses the pre-processed Human dendritic cell dataset [1] to perform batch integration.
Please note that for each data frame in the object meta
, there should be two columns named cell_id
and cell_type
. For instance, let meta_i
be a data frame under meta
, and there should be two columns meta_i$cell_id
and meta_i$cell_type
. If the cell type information is not available, any values put in meta_i$cell_type
should work.
library(SCIBER) rm(list = ls()) set.seed(7) data(HumanDC) exp <- HumanDC[["exp"]] meta <- HumanDC[["metadata"]] # Specify the proportion for each query batch to integrate batches. omega <- c() omega[[1]] <- 0.6 res <- SCIBER(input_batches = exp, ref_index = 1, batches_meta_data = meta, omega = omega, n_core = 1)
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