| create_seurat_object | R Documentation |
This function creates Seurat object for each sample in the metadata file. It also allows the user to perform SoupX (ambient RNA removal) and Scrublet (doublet detection) analysis.
create_seurat_object(
data_dir,
sample_meta = NULL,
sample_meta_filename = NULL,
meta_colnames = c("donor", "condition", "pass_qc"),
plot_dir = NULL,
use_scrublet = TRUE,
use_soupx = FALSE,
tenx_dir = "premrna_outs",
tenx_counts_dir = "filtered_feature_bc_matrix",
expected_doublet_rate = 0.06,
min.cells = 10,
min.features = 200,
...
)
data_dir |
Parent directory where all sample 10x files are stored. Think of it as project directory. |
sample_meta |
Sample metadata information in a Data.frame like object. Columns should at least contain 'sample', 'donor', 'condition' and 'pass_qc'. |
sample_meta_filename |
Filename of sample metadata information, same as 'meta' parameter above. User should provide one of 'meta' or 'meta_filename'. |
meta_colnames |
Sample metadata column names to store in Seurat metadata. |
plot_dir |
Directory for storing QC plots. Used if use_soupx = TRUE. |
use_scrublet |
Logical, wether to use Scrublet for doublet detection. |
use_soupx |
Logical, wether to use SoupX for ambient RNA removal. |
tenx_dir |
Name of 10x base directory, e.g. with outputs after running cellranger. Default 'premrna_outs', i.e. assumes single-nuclei RNA-seq. |
tenx_counts_dir |
Name of 10x directory where count matrices are stored. Default 'filtered_feature_bc_matrix' |
expected_doublet_rate |
The expected fraction of transcriptomes that are doublets, typically 0.05 - 0.1 |
min.cells |
Include features/genes detected in at least this many cells. |
min.features |
Include cells where at least this many features/genes are detected. |
... |
Additional named parameters passed to Seurat, Scrublet or SoupX. |
List of Seurat objects equal the number of samples in the sample metadata file. If a single sample, returns a Seurat object.
C.A.Kapourani C.A.Kapourani@ed.ac.uk
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