
Load in h5ad to SingleCells
load_h5ad.RdThis function takes an h5ad file and loads the obs and var data into the
DuckDB of the SingleCells class and the counts into a Rust-binarised
format for rapid access. During the reading in of the counts, the log CPM
transformation will occur automatically.
Usage
load_h5ad(
object,
h5_path,
sc_qc_param = params_sc_min_quality(),
streaming = 1L,
raw_count_slot = c("auto", "X", "raw.X", "layers.counts"),
cell_id_col = NULL,
batch_size = 1000L,
max_genes_in_memory = 2000L,
cell_batch_size = 100000L,
.verbose = TRUE
)Arguments
- object
SingleCellsclass.- h5_path
File path to the h5ad object you wish to load in.
- sc_qc_param
List. Output of
params_sc_min_quality(). A list with the following elements:min_unique_genes - Integer. Minimum number of genes to be detected in the cell to be included.
min_lib_size - Integer. Minimum library size in the cell to be included.
min_cells - Integer. Minimum number of cells a gene needs to be detected to be included.
target_size - Float. Target size to normalise to. Defaults to
1e5.
- streaming
Integer.
0L-> all cells loaded in memory then transposed (fastest, highest memory),1L-> light streaming with cell batching,2L-> heavy streaming with memory upper boundaries on the gene side. Controls memory pressure during the CSR-to-CSC conversion. Defaults to1L.- raw_count_slot
Where raw counts live.
"auto"detects per file viadetect_raw_count_slot(); otherwise one of"X","raw.X","layers.counts".- cell_id_col
Optional string. If a specific column in the h5ad obs data is representing the cell identifiers, you can specify it here.
- batch_size
Integer. Cell batch size when
streaming = 1L. Defaults to1000L.- max_genes_in_memory
Integer. Maximum genes held in memory at once when
streaming = 2L. Defaults to2000L.- cell_batch_size
Integer. Cell batch size when
streaming = 2L. Defaults to100000L.- .verbose
Boolean. Controls the verbosity of the function.
Examples
# round trip through a sparse h5ad file
data <- generate_single_cell_test_data(
syn_data_params = params_sc_synthetic_data(n_cells = 200L, n_genes = 40L)
)
f_path <- tempfile(fileext = ".h5ad")
write_h5ad_sc(f_path, data$counts, data$obs, data$var, .verbose = FALSE)
dir_data <- tempfile("sc_h5ad")
dir.create(dir_data, recursive = TRUE)
sc <- load_h5ad(
object = SingleCells(dir_data = dir_data),
h5_path = f_path,
sc_qc_param = params_sc_min_quality(
min_unique_genes = 5L,
min_lib_size = 25L,
min_cells = 5L
),
streaming = 0L,
.verbose = FALSE
)
dim(sc)
#> [1] 200 40
unlink(c(f_path, dir_data), recursive = TRUE, force = TRUE)