DifferentialRegulation: a method to identify genes displaying differential regulation between groups of samples
04/15/2025
Package
DifferentialRegulation 2.6.0
Contents
1 Introduction
DifferentialRegulation is a method for detecting differentially regulated genes between two groups of samples (e.g., healthy vs. disease, or treated vs. untreated samples), by targeting differences in the balance of spliced (S) and unspliced (U) mRNA abundances. The method fits both bulk and single-cell RNA-sequencing (scRNA-seq) data: on bulk data, DifferentialRegulation targets changes (across all cells) at the transcript level, while on single-cell data, it targets cell-type specific changes at the gene-level.
Below, we briefly illustrate the main conceptual and mathematical aspects. For more details, a pre-print will follow shortly.
1.1 Conceptual idea
DifferentialRegulation is based on a similar rationale to RNA velocity tools, notably velocyto (La Manno et al. 2018) and scVelo (Bergen et al. 2020), which compare spliced and unspliced abundances to their equilibrium levels.
Intuitively, if a large fraction of U is present for a gene, this will be spliced and increase the relative abundance of S. Conversely, if a small fraction of U is present for a gene, the newly spliced mRNA will not compensate the degradation of the (already) spliced mRNA, and the proportion of S will decrease in the short term. Therefore, in the two examples above, the gene is currently being up- and down-regulated, respectively; i.e., gene expression is going to increase and decrease, respectively.
We extend this argument to compare the relative abundances of S and U reads across groups of samples. In particular, a higher proportion of unspliced (spliced) mRNA in a condition suggests that a gene is currently being up- (down-) regulated compared to the other condition.
While canonical differential gene expression focuses on changes in overall gene abundance, DifferentialRegulation discovers differences (between conditions) in the near future changes of (spliced) gene expression (conceptually similar to the derivative of S respect to time).
Similarly to RNA velocity tools, DifferentialRegulation is an instrument to facilitate discoveries in the context of development.
1.2 Mathematical details
From a mathematical point of view, DifferentialRegulation accounts for the sample-to-sample variability, and embeds multiple samples in a Bayesian hierarchical model. Furthermore, our method also deals with two major sources of mapping uncertainty: i) ‘ambiguous’ reads, compatible with both spliced and unspliced versions of a gene or transcript, and ii) reads mapping to multiple genes or transcripts. When using scRNA-seq data, ambiguous reads are considered separately from spliced and unsplced reads, while reads that are compatible with multiple genes are treated as latent variables and allocated to the gene of origin. When using bulk RNA-seq data, we allocate both ambiguous reads and reads mapping to multiple transcripts: the former ones are allocated to the spliced or unspliced version of each trascript, while the latter ones are allocated to the transcript of origin.
DifferentialRegulation uses two nested models.
In single-cell RNA-seq data:
a Dirichlet-multinomial (\(DM\)) for the proportions of unspliced, spliced and ambiguous (USA) reads in each gene: \(DM(\pi_U, \pi_S, \pi_A, \delta)\), where \(\pi_U, \pi_S, \pi_A\) indicate the (group-level) relative abundances of U, S and A counts, and \(\delta\) represents the precision parameter, modelling the degree of over-dispersion between samples;
a multinomial (\(MN\)) for the (sample-specific) relative abundance of genes in each sample: \(MN(\pi^i_1, ..., \pi^i_{n_g})\), where \(\pi^i_g\) is the relative abundance of the \(g\)-th gene in the \(i\)-th sample.
In bulk RNA-seq data:
a Dirichlet-multinomial (\(DM\)) for the proportions of unspliced and spliced (US) reads in each transcript: \(DM(\pi_U, \pi_S, \delta)\), where \(\pi_U, \pi_S\) indicate the (group-level) relative abundances of U and S counts, and \(\delta\) represents the precision parameter, modelling the degree of over-dispersion between samples;
a multinomial (\(MN\)) for the (sample-specific) relative abundance of transcripts in each sample: \(MN(\pi^i_1, ..., \pi^i_{n_t})\), where \(\pi^i_t\) is the relative abundance of the \(t\)-th transcript in the \(i\)-th sample.
The \(DM\) model is the main focus here, and the one which is used for differential testing between conditions, while the \(MN\) model is necessary for allocating reads across genes.
Parameters are inferred via Markov chain Monte Carlo (MCMC) techniques (Metropolis-within-Gibbs), and differential testing is performed by comparing \((\pi_U, \pi_S, \pi_A)\) (single-cell data) or \((\pi_U, \pi_S)\) (bulk data) or between conditions.
1.3 Bioconductor installation
DifferentialRegulation is available on Bioconductor and can be installed with the command:
if (!requireNamespace("BiocManager", quietly=TRUE))
install.packages("BiocManager")
BiocManager::install("DifferentialRegulation")To access the R code used in the vignettes, type:
browseVignettes("DifferentialRegulation")1.4 Questions, issues and citation
Questions relative to DifferentialRegulation should be reported as a new issue at BugReports.
To cite DifferentialRegulation, type:
citation("DifferentialRegulation")## To cite DifferentialRegulation in publications use:
##
## Simone Tiberi, Joel Meili, Peiying Cai, Charlotte Soneson, Dongze He,
## Hirak Sarkar, Alejandra Avalos-Pacheco, Rob Patro, Mark D. Robinson
## (2024). DifferentialRegulation: a Bayesian hierarchical approach to
## identify differentially regulated genes. Biostatistics. URL
## https://doi.org/10.1093/biostatistics/kxae017
##
## A BibTeX entry for LaTeX users is
##
## @Article{,
## title = {DifferentialRegulation: a Bayesian hierarchical approach to identify differentially regulated genes},
## author = {Simone Tiberi and Joel Meili and Peiying Cai and Charlotte Soneson and Dongze He and Hirak Sarkar and Alejandra Avalos-Pacheco and Rob Patro and Mark D. Robinson},
## eprint = {https://doi.org/10.1093/biostatistics/kxae017},
## journal = {Biostatistics},
## year = {2024},
## doi = {10.1093/biostatistics/kxae017},
## url = {https://doi.org/10.1093/biostatistics/kxae017},
## }2 Single-cell RNA-seq pipeline
2.1 Input data: alignment and quantification with alevin-fry
DifferentialRegulation inputs scRNA-seq data, aligned via alevin-fry (He et al. 2022).
NOTE: when using alevin-fry, set options:
--d(or--dump-eqclasses), to obtain the equivalence classes;--use-mtx, to store counts in aquants_mat.mtxfile (as expected by ourload_USAfunction).
We also recommend using the --CR-like-EM option, which also allows equivalence classes of reads that map to multiple genes.
alevin-fry software: https://github.com/COMBINE-lab/alevin-fry
alevin-fry documentation: https://alevin-fry.readthedocs.io/en/latest/index.html
alevin-fry tutorial to obtain USA mapping: https://combine-lab.github.io/alevin-fry-tutorials/2021/improving-txome-specificity/
2.2 Load the package
Load DifferentialRegulation.
library(DifferentialRegulation)2.3 Load the data
We use a real droplet scRNA-seq dataset from Velasco et al. (2019). In particular, we compare two groups of three samples, consisting of human brain organoids, cultured for 3 and 6 months. For computational reasons, we stored a subset of this dataset, in our package, consisting of 100 genes and 3,493 cells, belonging to two cell-types. Cell-type assignment was done in the original styudy (Velasco et al. 2019). For more information about the data, refer to the original study here.
We specify the directory of the data (internal in the package).
data_dir = system.file("extdata", package = "DifferentialRegulation")Specify the directory of the USA (unspliced, spliced and ambiguous) estimated counts, inferred via alevin-fry.
# specify samples ids:
sample_ids = paste0("organoid", c(1:3, 16:18))
# set directories of each sample input data (obtained via alevin-fry):
base_dir = file.path(data_dir, "alevin-fry", sample_ids)
# Note that alevin-fry needs to be run with `--use-mtx` option to store counts in a `quants_mat.mtx` file.
path_to_counts = file.path(base_dir,"/alevin/quants_mat.mtx")
path_to_cell_id = file.path(base_dir,"/alevin/quants_mat_rows.txt")
path_to_gene_id = file.path(base_dir,"/alevin/quants_mat_cols.txt")Specify the directory of the ECs and respective counts, inferred via alevin-fry.
path_to_EC_counts = file.path(base_dir,"/alevin/geqc_counts.mtx")
path_to_EC = file.path(base_dir,"/alevin/gene_eqclass.txt.gz")2.3.1 Load USA counts
Load the unspliced, spliced and ambiguous (USA) estimated counts, quantified by alevin-fry, in a SingleCellExperiment.
By default, counts (stored in assays(sce)$counts) are defined as summation of spliced read and 50% of ambiguous reads (i.e., reads compatible with both spliced and unspliced versions of a gene): counts = spliced + 0.5 * ambiguous.
sce = load_USA(path_to_counts,
path_to_cell_id,
path_to_gene_id,
sample_ids)
sce## class: SingleCellExperiment
## dim: 100 3493
## metadata(0):
## assays(4): spliced unspliced ambiguous counts
## rownames(100): ENSG00000223972.5 ENSG00000243485.5 ...
## ENSG00000162592.10 ENSG00000235169.11
## rowData names(0):
## colnames(3493): organoid1.GCCTCTAGTCGGATCC organoid1.GAACATCGTCTGATCA
## ... organoid18.AGCGTCGAGCGCCTCA organoid18.GATCGCGTCGTTACGA
## colData names(1): sample_id
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):Cell types should be assigned to each cell; here we load pre-computed cell types.
path_to_DF = file.path(data_dir,"DF_cell_types.txt")
DF_cell_types = read.csv(path_to_DF, sep = "\t", header = TRUE)
matches = match(colnames(sce), DF_cell_types$cell_id)
sce$cell_type = DF_cell_types$cell_type[matches]
table(sce$cell_type)##
## Cycling RG
## 2399 10942.3.2 Load equivalence classes (EC)
Load the equivalence classes and respective counts.
EC_list = load_EC(path_to_EC_counts,
path_to_EC,
path_to_cell_id,
path_to_gene_id,
sample_ids)## The percentage of multi-gene mapping reads in sample 'organoid1' is: 11.09## The percentage of multi-gene mapping reads in sample 'organoid2' is: 13.53## The percentage of multi-gene mapping reads in sample 'organoid3' is: 7.19## The percentage of multi-gene mapping reads in sample 'organoid16' is: 8.59## The percentage of multi-gene mapping reads in sample 'organoid17' is: 3.75## The percentage of multi-gene mapping reads in sample 'organoid18' is: 6.76For every sample, load_EC prints the percentage of reads compatible with multiple genes (i.e., multi-gene mapping reads).
Here multi-gene reads are relatively low, because we are considering a subset of 100 genes only; however, in the full dataset we found that approximately 40% of reads map to multiple genes.
Intuitively, the larger these numbers, the greater the benefits one may achieve by using ECs and modelling the variability of these uncertain gene allocations.
2.4 QC and filtering
Quality control (QC) and filtering of low quality cells can be performed as usual on the sce object.
The sce object computed via load_USA contains a counts assays, defined as the summation of spliced counts and 50% of ambiguous counts.
For examples of QC, you can refer to the OSCA book (Amezquita et al. 2020).
Importantly, cells only need to be filtered in the sce object, and NOT in the EC_list object: cells that are filtered in sce will also be removed from ECs by compute_PB_counts function.
2.5 Differential testing
First, we define the design of the study: in our case we have 2 groups, that we call “A” and “B” of 2 samples each.
design = data.frame(sample = sample_ids,
group = c( rep("3 mon", 3), rep("6 mon", 3) ))
design## sample group
## 1 organoid1 3 mon
## 2 organoid2 3 mon
## 3 organoid3 3 mon
## 4 organoid16 6 mon
## 5 organoid17 6 mon
## 6 organoid18 6 monCompute pseudo-bulk (PB) onbject needed for differential testing.
PB_counts = compute_PB_counts(sce = sce,
EC_list = EC_list,
design = design,
sample_col_name = "sample",
group_col_name = "group",
sce_cluster_name = "cell_type")## the following cell clusters (e.g., cell types) have more than 100 cells and will be analyzed:## Cycling --- RGNB: to reduce memory usage, we can remove the EC_list object, which typically requires a large amount of memory, particularly in large datasets.
If needed, the sce object can be removed as well, since it is not needed for differential testing.
rm(EC_list)We perform differential testing:
# EC-based test:
set.seed(1609612)
results = DifferentialRegulation(PB_counts,
n_cores = 2,
traceplot = TRUE)2.6 Visualizing results
DifferentialRegulation function returns of a list of 4 data.frames:
Differential_results, which contains results from differential testing only;US_results, that has results for the proportion of Spliced and Unspliced counts (where Ambiguous counts are allocated 50:50 to Spliced and Unspliced);USA_results, which includes results for the proportion of Spliced, Unspliced and Ambiguous counts (Ambiguous counts are reported separately from Spliced and Unspliced counts);Convergence_results, that contains information about convergence of posterior chains.
names(results)## [1] "Differential_results" "US_results" "USA_results"
## [4] "Convergence_results" "MCMC_U"In Differential_results element, columns Gene_id and Cluster_id contain the gene and cell-cluster name, while p_val, p_adj.loc and p_adj.glb report the raw p-values, locally and globally adjusted p-values, via Benjamini and Hochberg (BH) correction.
In locally adjusted p-values (p_adj.loc) BH correction is applied to each cluster separately, while in globally adjusted p-values (p_adj.glb) BH correction is performed to the results from all clusters.
head(results$Differential_results, 3)## Gene_id Cluster_id p_val p_adj.glb p_adj.loc Prob-6 mon-UP
## 31 ENSG00000179403.12 RG 0.01702780 0.2527751 0.2271129 0.004666667
## 5 ENSG00000157933.10 Cycling 0.25362515 0.8454172 0.7608754 0.010000000
## 12 ENSG00000197530.12 Cycling 0.02393744 0.2527751 0.2527751 0.010000000The final column of results$Differential_results, Prob-group_name-UP, indicates the probability that a gene is UP-regulated in one group (6 mon in this case) compared to the other group.
This column can be used to sort genes, by the probability that they are being up-regulated in group 6 mon:
ordering_UP = order(results$Differential_results[,6], decreasing = TRUE)
head(results$Differential_results[ordering_UP,], 3)## Gene_id Cluster_id p_val p_adj.glb p_adj.loc Prob-6 mon-UP
## 17 ENSG00000227775.3 Cycling 0.03159689 0.2527751 0.2527751 0.9973333
## 13 ENSG00000197785.14 Cycling 0.84706492 0.9750586 0.9705238 0.9293333
## 34 ENSG00000197785.14 RG 0.82842935 0.9750586 0.9743574 0.8726667Alternatively, one can sort genes by their probability of currently being down-regulated in group 6 mon (or conversely, up-regularted in the alternative group, 3mon):
ordering_DOWN = order(results$Differential_results[,6], decreasing = FALSE)
head(results$Differential_results[ordering_DOWN,], 3)## Gene_id Cluster_id p_val p_adj.glb p_adj.loc Prob-6 mon-UP
## 31 ENSG00000179403.12 RG 0.01702780 0.2527751 0.2271129 0.004666667
## 5 ENSG00000157933.10 Cycling 0.25362515 0.8454172 0.7608754 0.010000000
## 12 ENSG00000197530.12 Cycling 0.02393744 0.2527751 0.2527751 0.010000000In US_results and USA_results elements, pi and sd indicate the estimated proportion and standard deviation, respectively, S, U and A refer to Spliced, Unspliced and Ambiguous counts, respectively, while 3 mon and 6 mon refer to the groups, as named in the design.
For instance, columns pi_S-3 mon and sd_S-3 mon indicate the estimate (posterior mean) and standard deviation (sd) for the proportion of Spliced (pi_S) and Unspliced (pi_U) counts in group 3 mon, respectively.
We visualize US results.
head(results$US_results, 3)## Gene_id Cluster_id p_val p_adj.glb p_adj.loc Prob-6 mon-UP
## 31 ENSG00000179403.12 RG 0.01702780 0.2527751 0.2271129 0.004666667
## 5 ENSG00000157933.10 Cycling 0.25362515 0.8454172 0.7608754 0.010000000
## 12 ENSG00000197530.12 Cycling 0.02393744 0.2527751 0.2527751 0.010000000
## pi_S-3 mon pi_U-3 mon pi_S-6 mon pi_U-6 mon sd_S-3 mon sd_U-3 mon sd_S-6 mon
## 31 0.60280253 0.3971975 0.9580279 0.04197211 0.14499713 0.14499713 0.04702326
## 5 0.02351666 0.9764833 0.1974490 0.80255101 0.02653935 0.02653935 0.09575482
## 12 0.44962146 0.5503785 0.8170496 0.18295039 0.13969280 0.13969280 0.03817278
## sd_U-6 mon
## 31 0.04702326
## 5 0.09575482
## 12 0.03817278We visualize USA results.
head(results$USA_results, 3)## Gene_id Cluster_id p_val p_adj.glb p_adj.loc Prob-6 mon-UP
## 31 ENSG00000179403.12 RG 0.01702780 0.2527751 0.2271129 0.004666667
## 5 ENSG00000157933.10 Cycling 0.25362515 0.8454172 0.7608754 0.010000000
## 12 ENSG00000197530.12 Cycling 0.02393744 0.2527751 0.2527751 0.010000000
## pi_S-3 mon pi_U-3 mon pi_A-3 mon pi_S-6 mon pi_U-6 mon pi_A-6 mon
## 31 0.32469407 0.1190890 0.556216926 0.9292102 0.01315445 0.05763533
## 5 0.01872584 0.9716925 0.009581638 0.1305360 0.73563802 0.13382598
## 12 0.28148866 0.3822457 0.336265611 0.7642271 0.13012789 0.10564501
## sd_S-3 mon sd_U-3 mon sd_A-3 mon sd_S-6 mon sd_U-6 mon sd_A-6 mon
## 31 0.20797530 0.12195424 0.17932220 0.07453247 0.02936422 0.06316600
## 5 0.02626491 0.02792489 0.01104273 0.07469199 0.14825977 0.13580783
## 12 0.17266473 0.16050666 0.18191944 0.05059876 0.03802437 0.04672828We can also visualize information about the convergence of the posterior chains.
results$Convergence_results## Cluster_id burn_in N_MCMC first_chain second_chain
## 1 Cycling 500 2000 converged NOT run (1st chain converged)
## 2 RG 500 2000 converged NOT run (1st chain converged)Finally, we can plot the estimated proportions of spliced and unspliced reads.
If CI = TRUE (default option), for each estimate, we can also add the respective profile Wald type confidence interval, of level CI_level (0.95 by default).
Similarly to above, we can plot the proportion of US or USA reads. Note that, although US reads are easier to interpret, USA reads more closely reflect what is being compared between conditions.
plot_pi(results,
type = "US",
gene_id = results$Differential_results$Gene_id[1],
cluster_id = results$Differential_results$Cluster_id[1])
plot_pi(results,
type = "US",
gene_id = results$Differential_results$Gene_id[2],
cluster_id = results$Differential_results$Cluster_id[2])
plot_pi(results,
type = "USA",
gene_id = results$Differential_results$Gene_id[1],
cluster_id = results$Differential_results$Cluster_id[1])
plot_pi(results,
type = "USA",
gene_id = results$Differential_results$Gene_id[2],
cluster_id = results$Differential_results$Cluster_id[2])
If traceplot = TRUE in DifferentialRegulation, can also plot the posterior chains of \(\pi_U\) (i.e., the group-level relative abundances of U) in both groups.
The vertical dashed grey line indicates the burn-in that was used (i.e., the iterations to the left side of the line were excluded).
Note that, to decrease memory requirements, the burn-in is not returned.
plot_traceplot(results,
gene_id = results$Differential_results$Gene_id[1],
cluster_id = results$Differential_results$Cluster_id[1])
plot_traceplot(results,
gene_id = results$Differential_results$Gene_id[2],
cluster_id = results$Differential_results$Cluster_id[2])
3 Bulk RNA-seq pipeline
3.1 Input data: alignment and quantification with salmon or kallisto
DifferentialRegulation inputs bulk RNA-seq data.
Firstly, we should generate an expanded reference transcriptome, containing both spliced and unsplced versions of each transcript. The code to generate such a reference can be found here.
Then, using the extended reference, alignment and quantification can be performed via salmon (Patro et al. 2017) or kallisto (Bray et al. 2016).
NOTE:
- when using salmon, use the option --dumpEq to obtain the equivalence classes;
- when using kallisto, run both kallisto quant and kallisto pseudo to obtain the transcript estimated counts and equivalence classes, respectively.
salmon software: https://combine-lab.github.io/salmon/
kallisto software: https://pachterlab.github.io/kallisto/about
3.2 Load the package
Load DifferentialRegulation.
library(DifferentialRegulation)3.3 Load the data
Here, we use a small simulated dataset (human genome), made of two groups of three samples each, where differential effects were artificially introduced in a sub-set of transcripts.
The scripts to generate this simulated data can be found here. Here we use the small simulation (called subset), based on chromosome 22 only.
We specify the directory of the data (internal in the package).
data_dir = system.file("extdata", package = "DifferentialRegulation")Specify the path to the data (counts and equivalence classes).
# specify samples ids:
sample_ids = paste0("sample", seq_len(6))
# US estimates:
quant_files = file.path(data_dir, "salmon", sample_ids, "quant.sf")
file.exists(quant_files)## [1] TRUE TRUE TRUE TRUE TRUE TRUE# Equivalence classes:
equiv_classes_files = file.path(data_dir, "salmon", sample_ids, "aux_info/eq_classes.txt.gz")
file.exists(equiv_classes_files)## [1] TRUE TRUE TRUE TRUE TRUE TRUE3.3.1 Load US counts
Load the unspliced and spliced (US) estimated counts, quantified by salmon, in a SummarizedExperiment.
SE = load_bulk_US(quant_files,
sample_ids)## reading in files with read_tsv## 1 2 3 4 5 63.3.2 Load equivalence classes (EC)
Load the equivalence classes and respective counts.
EC_list = load_bulk_EC(path_to_eq_classes = equiv_classes_files,
n_cores = 2)## The percentage of multi-mapping reads in sample 1 is: 94## The percentage of multi-mapping reads in sample 2 is: 94## The percentage of multi-mapping reads in sample 3 is: 94## The percentage of multi-mapping reads in sample 4 is: 93## The percentage of multi-mapping reads in sample 5 is: 93## The percentage of multi-mapping reads in sample 6 is: 92For every sample, load_bulk_EC prints the percentage of multi-mapping reads; i.e., reads compatible with multiple transcripts, or to both spliced and unspliced versions of a trascript.
Intuitively, the larger these numbers, the greater the benefits one may achieve by using ECs and modelling the variability of these uncertain gene allocations.
3.4 QC and filtering
Quality control (QC) and filtering of low quality cells can be performed as usual on the SE object, using the spliced assay.
Importantly, cells only need to be filtered in the SE object, and NOT in the EC_list object: cells that are filtered in SE will also be removed from ECs when running DifferentialRegulation_bulk function.
3.5 Differential testing
First, we define the design of the study: in our case we have 2 groups, that we call “A” and “B” of 2 samples each.
group_names = rep(c("A", "B"), each = 3)
design = data.frame(sample = sample_ids,
group = group_names)
design## sample group
## 1 sample1 A
## 2 sample2 A
## 3 sample3 A
## 4 sample4 B
## 5 sample5 B
## 6 sample6 BWe perform differential testing.
As above, if traceplot = TRUE the function also returns the posterior chains of \(\pi_U\) (i.e., the group-level relative abundances of U) in both groups (MCMC_U object), which can then be visualized via plot_bulk_traceplot function.
Again, the vertical dashed grey line represents the burn-in.
# EC-based test:
set.seed(1609612)
results = DifferentialRegulation_bulk(SE = SE,
EC_list = EC_list,
design = design,
n_cores = 2,
traceplot = TRUE)## 714 transcripts pass filtering and will be analyzed.## Estimating gene-wise precision parameters## Estimation completed## Starting the MCMC## MCMC completed and successfully converged.3.6 Visualizing results
DifferentialRegulation function returns of a list of 2 data.frames:
Differential_results, which contains results from differential testing, and estimates of the proportion of Spliced and Unspliced reads in each group;Convergence_results, that contains information about convergence of posterior chains.
names(results)## [1] "Differential_results" "Convergence_results" "MCMC_U"In Differential_results element, column Transcript_id contains the transcript name, while p_val and p_adj report the raw and adjusted p-values, via Benjamini and Hochberg (BH) correction.
Prob-group_name-UP, indicates the probability that a gene is UP-regulated in one group (B in this case) compared to the other group.
Names pi and sd indicate the estimated proportion and standard deviation, respectively, S and U refer to Spliced and Unspliced counts, respectively, while A and B refer to the groups, as named in the design.
For instance, columns pi_S-B and sd_S-B indicate the estimate (posterior mean) and standard deviation (sd) for the proportion of Spliced (pi_S) and Unspliced (pi_U) counts in group B, respectively.
head(results$Differential_results, 3)## Transcript_id p_val p_adj Prob-B-UP pi_S-A pi_U-A
## 405 ENST00000455558.2 0.01306881 0.2926763 0.0006666667 0.02236814 0.9776319
## 489 ENST00000475941.1 0.04195051 0.7513694 0.0333333333 0.18076359 0.8192364
## 352 ENST00000437122.1 0.37595245 0.9999918 0.1280000000 0.08693849 0.9130615
## pi_S-B pi_U-B sd_S-A sd_U-A sd_S-B sd_U-B
## 405 0.3329001 0.6670999 0.01836548 0.01836548 0.1211540 0.1211540
## 489 0.6213707 0.3786293 0.12237619 0.12237619 0.1878014 0.1878014
## 352 0.2607850 0.7392150 0.08816988 0.08816988 0.1646697 0.1646697We can also sort genes by the probability that they are being up-regulated in group B:
ordering_UP = order(results$Differential_results[,4], decreasing = TRUE)
head(results$Differential_results[ordering_UP,], 3)## Transcript_id p_val p_adj Prob-B-UP pi_S-A pi_U-A
## 92 ENST00000331728.9 7.621029e-05 6.801768e-03 1 0.6714835 0.3285165
## 98 ENST00000333130.4 2.727985e-07 6.492605e-05 1 0.8644982 0.1355018
## 174 ENST00000398822.7 1.721514e-03 6.469269e-02 1 0.5781232 0.4218768
## pi_S-B pi_U-B sd_S-A sd_U-A sd_S-B sd_U-B
## 92 0.02080984 0.9791902 0.1590060 0.1590060 0.05302101 0.05302101
## 98 0.02821470 0.9717853 0.1552249 0.1552249 0.06050581 0.06050581
## 174 0.05021898 0.9497810 0.1666666 0.1666666 0.03243535 0.03243535Alternatively, one can sort genes by their probability of currently being down-regulated in group B (or conversely, up-regularted in the alternative group, 3mon):
ordering_DOWN = order(results$Differential_results[,4], decreasing = FALSE)
head(results$Differential_results[ordering_DOWN,], 3)## Transcript_id p_val p_adj Prob-B-UP pi_S-A pi_U-A
## 405 ENST00000455558.2 0.01306881 0.2926763 0.0006666667 0.02236814 0.9776319
## 489 ENST00000475941.1 0.04195051 0.7513694 0.0333333333 0.18076359 0.8192364
## 352 ENST00000437122.1 0.37595245 0.9999918 0.1280000000 0.08693849 0.9130615
## pi_S-B pi_U-B sd_S-A sd_U-A sd_S-B sd_U-B
## 405 0.3329001 0.6670999 0.01836548 0.01836548 0.1211540 0.1211540
## 489 0.6213707 0.3786293 0.12237619 0.12237619 0.1878014 0.1878014
## 352 0.2607850 0.7392150 0.08816988 0.08816988 0.1646697 0.1646697We can also visualize information about the convergence of the posterior chains.
results$Convergence_results## burn_in N_MCMC first_chain second_chain
## 1 500 2000 converged NOT run (1st chain converged)Finally, we can plot the estimated proportions of spliced and unspliced reads.
If CI = TRUE (default option), for each estimate, we can also add the respective profile Wald type confidence interval, of level CI_level (0.95 by default).
plot_bulk_pi(results,
transcript_id = results$Differential_results$Transcript_id[1])
plot_bulk_pi(results,
transcript_id = results$Differential_results$Transcript_id[2])
If traceplot = TRUE in DifferentialRegulation_bulk, can also plot the posterior chains of \(\pi_U\) (i.e., the group-level relative abundances of U) in both groups.
Note that, to decrease memory requirements, the burn-in is not returned.
plot_bulk_traceplot(results,
transcript_id = results$Differential_results$Transcript_id[1])
plot_bulk_traceplot(results,
transcript_id = results$Differential_results$Transcript_id[2])
4 Session info
sessionInfo()## R version 4.5.0 RC (2025-04-04 r88126)
## Platform: x86_64-pc-linux-gnu
## Running under: Ubuntu 24.04.2 LTS
##
## Matrix products: default
## BLAS: /home/biocbuild/bbs-3.21-bioc/R/lib/libRblas.so
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.12.0 LAPACK version 3.12.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_GB LC_COLLATE=C
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: America/New_York
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats graphics grDevices utils datasets methods base
##
## other attached packages:
## [1] DifferentialRegulation_2.6.0 BiocStyle_2.36.0
##
## loaded via a namespace (and not attached):
## [1] tidyselect_1.2.1 dplyr_1.1.4
## [3] farver_2.1.2 R.utils_2.13.0
## [5] fastmap_1.2.0 SingleCellExperiment_1.30.0
## [7] digest_0.6.37 lifecycle_1.0.4
## [9] statmod_1.5.0 DRIMSeq_1.36.0
## [11] magrittr_2.0.3 compiler_4.5.0
## [13] rlang_1.1.6 sass_0.4.10
## [15] rngtools_1.5.2 tools_4.5.0
## [17] yaml_2.3.10 data.table_1.17.0
## [19] knitr_1.50 S4Arrays_1.8.0
## [21] labeling_0.4.3 doRNG_1.8.6.2
## [23] bit_4.6.0 DelayedArray_0.34.0
## [25] plyr_1.8.9 abind_1.4-8
## [27] BiocParallel_1.42.0 withr_3.0.2
## [29] BiocGenerics_0.54.0 R.oo_1.27.0
## [31] grid_4.5.0 stats4_4.5.0
## [33] colorspace_2.1-1 edgeR_4.6.0
## [35] ggplot2_3.5.2 scales_1.3.0
## [37] iterators_1.0.14 MASS_7.3-65
## [39] tinytex_0.57 SummarizedExperiment_1.38.0
## [41] cli_3.6.4 rmarkdown_2.29
## [43] crayon_1.5.3 generics_0.1.3
## [45] tzdb_0.5.0 httr_1.4.7
## [47] reshape2_1.4.4 cachem_1.1.0
## [49] stringr_1.5.1 parallel_4.5.0
## [51] BiocManager_1.30.25 XVector_0.48.0
## [53] matrixStats_1.5.0 vctrs_0.6.5
## [55] Matrix_1.7-3 jsonlite_2.0.0
## [57] bookdown_0.43 hms_1.1.3
## [59] IRanges_2.42.0 S4Vectors_0.46.0
## [61] bit64_4.6.0-1 archive_1.1.12
## [63] magick_2.8.6 locfit_1.5-9.12
## [65] foreach_1.5.2 limma_3.64.0
## [67] jquerylib_0.1.4 glue_1.8.0
## [69] codetools_0.2-20 stringi_1.8.7
## [71] gtable_0.3.6 GenomeInfoDb_1.44.0
## [73] GenomicRanges_1.60.0 UCSC.utils_1.4.0
## [75] BANDITS_1.24.0 munsell_0.5.1
## [77] tibble_3.2.1 pillar_1.10.2
## [79] htmltools_0.5.8.1 GenomeInfoDbData_1.2.14
## [81] R6_2.6.1 doParallel_1.0.17
## [83] tximport_1.36.0 vroom_1.6.5
## [85] evaluate_1.0.3 lattice_0.22-7
## [87] Biobase_2.68.0 readr_2.1.5
## [89] R.methodsS3_1.8.2 bslib_0.9.0
## [91] Rcpp_1.0.14 gridExtra_2.3
## [93] SparseArray_1.8.0 xfun_0.52
## [95] MatrixGenerics_1.20.0 pkgconfig_2.0.3References
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Bergen, Volker, Marius Lange, Stefan Peidli, F Alexander Wolf, and Fabian J Theis. 2020. “Generalizing Rna Velocity to Transient Cell States Through Dynamical Modeling.” Nature Biotechnology 38 (12): 1408–14.
Bray, Nicolas L, Harold Pimentel, Páll Melsted, and Lior Pachter. 2016. “Near-Optimal Probabilistic Rna-Seq Quantification.” Nature Biotechnology 34 (5): 525.
He, Dongze, Mohsen Zakeri, Hirak Sarkar, Charlotte Soneson, Avi Srivastava, and Rob Patro. 2022. “Alevin-fry unlocks rapid, accurate and memory-frugal quantification of single-cell RNA-seq data.” Nature Methods 19 (3): 316–22.
La Manno, Gioele, Ruslan Soldatov, Amit Zeisel, Emelie Braun, Hannah Hochgerner, Viktor Petukhov, Katja Lidschreiber, et al. 2018. “RNA Velocity of Single Cells.” Nature 560 (7719): 494–98.
Patro, Rob, Geet Duggal, Michael I Love, Rafael A Irizarry, and Carl Kingsford. 2017. “Salmon Provides Fast and Bias-Aware Quantification of Transcript Expression.” Nature Methods 14 (4): 417.
Velasco, Silvia, Amanda J Kedaigle, Sean K Simmons, Allison Nash, Marina Rocha, Giorgia Quadrato, Bruna Paulsen, et al. 2019. “Individual Brain Organoids Reproducibly Form Cell Diversity of the Human Cerebral Cortex.” Nature 570 (7762): 523–27.