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Blase Mapping Result

MappingResult-class.Rd

Created by map_best_bin()

Value

A MappingResult object

Slots

bulk_name

The name of the bulk sample being mapped.

best_bin

The bin that best matched the bulk sample.

best_correlation

The spearman's rho that the test geneset had between the winning bin and the bulk.

top_2_distance

The absolute difference between the best and second best mapping buckets. Higher indicates a less doubtful mapping.

confident_mapping

TRUE when the mapped bin's lower bound is higher than the maximum upper bound of the other bins.

history

A dataframe of the correlation score and confidence bounds for each bin. Access with mapping_history()

bootstrap_iterations

The number of iterations used during the bootstrap.

See also

map_best_bin()

Examples

counts_matrix <- matrix(
    c(seq_len(120) / 10, seq_len(120) / 5),
    ncol = 48, nrow = 5
)
sce <- SingleCellExperiment::SingleCellExperiment(assays = list(
    normcounts = counts_matrix, logcounts = log(counts_matrix)
))
colnames(sce) <- seq_len(48)
rownames(sce) <- as.character(seq_len(5))
sce$cell_type <- c(rep("celltype_1", 24), rep("celltype_2", 24))

sce$pseudotime <- seq_len(48) - 1
blase_data <- as.BlaseData(sce, pseudotime_slot = "pseudotime", n_bins = 4)
genes(blase_data) <- as.character(seq_len(5))

bulk_counts <- matrix(seq_len(15) * 10, ncol = 3, nrow = 5)
colnames(bulk_counts) <- c("A", "B", "C")
rownames(bulk_counts) <- as.character(seq_len(5))

# Map to bin
result <- map_best_bin(blase_data, "B", bulk_counts)
result
#> MappingResult for 'B': best_bin=1 correlation=1 top_2_distance=0
#> 	 Confident Result: FALSE (next max upper  1 )
#> 	 with history for scores against 4  bins
#> 	 Bootstrapped with 200 iterations

# Map all bulks to bin
results <- map_all_best_bins(blase_data, bulk_counts)

# Plot Heatmap
plot_mapping_result_heatmap(list(result))


# Plot Correlation
plot_mapping_result_corr(result)


# Plot populations
sce <- assign_pseudotime_bins(
    sce,
    pseudotime_slot = "pseudotime", n_bins = 4
)
plot_bin_population(sce, best_bin(result), group_by_slot = "cell_type")


# Getters
bulk_name(result)
#> [1] "B"
best_bin(result)
#> [1] 1
best_correlation(result)
#> [1] 1
top_2_distance(result)
#> [1] 0
confident_mapping(result)
#> [1] FALSE
mapping_history(result)
#>   bin correlation lower_bound upper_bound
#> 1   1           1           1           1
#> 2   2           1           1           1
#> 3   3           1           1           1
#> 4   4           1           1           1
bootstrap_iterations(result)
#> [1] 200