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Knit directory: multigroup_ctwas_analysis/
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For non-psychiatric traits, we ran a cTWAS analysis using sQTL data from all 49 GTEx tissues.
For psychiatric traits, we used only the 9 GTEx brain tissues.
We ranked tissues by their G-test p-values & Fisher p-values and selected those passing the Bonferroni threshold (0.05 divided by the number of tissues) for the multi-group cTWAS analysis.
Default settings were used for computing z-scores, assembling input data, and estimating model parameters.
Mem: 50g/node got killed, 100g/node
z_gene <- compute_gene_z(z_snp, weights, ncore=10)
res <- assemble_region_data(region_info,
z_snp,
z_gene,
weights,
snp_map,
maxSNP = Inf,
min_group_size = 100,
thin = 1,
adjust_boundary_genes = TRUE,
ncore = 15)
param <- est_param(region_data,
group_prior_var_structure = "shared_all",
null_method = "ctwas",
niter_prefit = 3,
min_gene = 0,
min_var = 2,
min_p_single_effect = 0.8,
niter = 200,
ncore = 15,
verbose=TRUE)
library(ctwas)
Warning: replacing previous import 'utils::download.file' by
'restfulr::download.file' when loading 'rtracklayer'
source("/project/xinhe/xsun/multi_group_ctwas/data/samplesize.R")
trait_nopsy <- c("LDL-ukb-d-30780_irnt","aFib-ebi-a-GCST006414","ATH_gtexukb","BMI-panukb","HB-panukb",
"Height-panukb","HTN-panukb","IBD-ebi-a-GCST004131","PLT-panukb","RA-panukb","RBC-panukb",
"SBP-ukb-a-360","T1D-GCST90014023","WBC-ieu-b-30","T2D-panukb")
trait_psy <- c("SCZ-ieu-b-5102","ASD-ieu-a-1185","BIP-ieu-b-5110","MDD-ieu-b-102","PD-ieu-b-7","ADHD-ieu-a-1183","NS-ukb-a-230")
DT::datatable(matrix())
folder_results <- "/project/xinhe/xsun/multi_group_ctwas/21.tissue_selection_0511/results/S_thin1_shared_all_mingene0/"
converge_df <- c()
for (trait in trait_nopsy){
param <- readRDS(paste0(folder_results,trait,"/",trait,".thin1.shared_all.param.RDS"))
gwas_n <- samplesize[trait]
param_summarized_fisher <- summarize_param(param = param,gwas_n = gwas_n,enrichment_test = "fisher",alternative = "greater")
param_summarized_G <- summarize_param(param = param,gwas_n = gwas_n,enrichment_test = "G")
param_df <- data.frame(
group = names(param_summarized_fisher$group_size),
group_size = as.numeric(param_summarized_fisher$group_size[names(param_summarized_fisher$group_size)]),
group_pve = as.numeric(param_summarized_fisher$group_pve[names(param_summarized_fisher$group_size)]),
prop_heritability = as.numeric(param_summarized_fisher$prop_heritability[names(param_summarized_fisher$group_size)]),
log_enrichment = as.numeric(param_summarized_fisher$log_enrichment[names(param_summarized_fisher$group_size)]),
log_enrichment_se = as.numeric(param_summarized_fisher$log_enrichment_se[names(param_summarized_fisher$group_size)]),
enrichment_pval_fisher = as.numeric(param_summarized_fisher$enrichment_pval[names(param_summarized_fisher$group_size)]),
enrichment_pval_G = as.numeric(param_summarized_G$enrichment_pval[names(param_summarized_G$group_size)])
)
param_df$total_pve <- param_summarized_fisher$total_pve
param_df$prop_heritability <- paste0(round(param_df$prop_heritability * 100, 5), "%")
param_df <- param_df[order(param_df$enrichment_pval_fisher,decreasing = F),]
param_df_qtl <- param_df[-nrow(param_df),]
threshold <- 0.05/(nrow(param_df_qtl)-1)
cat("<br>")
cat(knitr::knit_print(DT::datatable(param_df, caption = htmltools::tags$caption( style = 'caption-side: left; text-align: left; color:black; font-size:150% ;',trait,options = list(pageLength = 10)))))
cat("<br>")
cat("<br>")
cat("<br>")
print(paste0("p-value cutoff(0.05/num_tissue) = ",threshold))
cat("<br>")
cat("<br>")
cat(paste0("Number of selected tissue -- fisher = ",min(10,sum(param_df_qtl$enrichment_pval_fisher < threshold)),"\n"))
cat("<br>")
cat(paste0(
head(param_df_qtl$group[param_df_qtl$enrichment_pval_fisher < threshold], 10),
collapse = " "
))
cat("<br>")
cat("<br>")
cat("<br>")
cat(paste0("Number of selected tissue -- G = ",min(10,sum(param_df_qtl$enrichment_pval_G < threshold)),"\n"))
cat("<br>")
cat(paste0(
head(param_df_qtl$group[param_df_qtl$enrichment_pval_G < threshold], 10),
collapse = " "
))
cat("<br>")
cat("<br>")
cat("<br>")
EM_iter <- length(param$loglik_iters)
converge <- param$converged
converge_df <- rbind(converge_df,c(trait,EM_iter,converge))
}
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 8
Whole_Blood|sQTL Adipose_Visceral_Omentum|sQTL Ovary|sQTL
Skin_Not_Sun_Exposed_Suprapubic|sQTL Artery_Aorta|sQTL Liver|sQTL
Muscle_Skeletal|sQTL Brain_Cerebellum|sQTL
Number of selected
tissue – G = 8
Whole_Blood|sQTL Adipose_Visceral_Omentum|sQTL
Ovary|sQTL Skin_Not_Sun_Exposed_Suprapubic|sQTL Artery_Aorta|sQTL
Liver|sQTL Muscle_Skeletal|sQTL
Brain_Cerebellum|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 7
Heart_Left_Ventricle|sQTL Muscle_Skeletal|sQTL
Heart_Atrial_Appendage|sQTL Testis|sQTL Colon_Sigmoid|sQTL
Adipose_Subcutaneous|sQTL
Brain_Putamen_basal_ganglia|sQTL
Number of selected tissue –
G = 7
Heart_Left_Ventricle|sQTL Muscle_Skeletal|sQTL
Heart_Atrial_Appendage|sQTL Testis|sQTL Colon_Sigmoid|sQTL
Adipose_Subcutaneous|sQTL
Brain_Putamen_basal_ganglia|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 9
Prostate|sQTL Minor_Salivary_Gland|sQTL Lung|sQTL Thyroid|sQTL
Artery_Aorta|sQTL Skin_Not_Sun_Exposed_Suprapubic|sQTL
Cells_EBV-transformed_lymphocytes|sQTL Skin_Sun_Exposed_Lower_leg|sQTL
Testis|sQTL
Number of selected tissue – G = 9
Prostate|sQTL Minor_Salivary_Gland|sQTL Lung|sQTL Thyroid|sQTL
Artery_Aorta|sQTL Skin_Not_Sun_Exposed_Suprapubic|sQTL
Cells_EBV-transformed_lymphocytes|sQTL Skin_Sun_Exposed_Lower_leg|sQTL
Testis|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 4
Esophagus_Muscularis|sQTL Brain_Cerebellum|sQTL
Brain_Caudate_basal_ganglia|sQTL
Esophagus_Gastroesophageal_Junction|sQTL
Number of selected
tissue – G = 10
Esophagus_Muscularis|sQTL Brain_Cerebellum|sQTL
Brain_Caudate_basal_ganglia|sQTL
Esophagus_Gastroesophageal_Junction|sQTL Adipose_Visceral_Omentum|sQTL
Adrenal_Gland|sQTL Breast_Mammary_Tissue|sQTL
Cells_Cultured_fibroblasts|sQTL Colon_Sigmoid|sQTL
Colon_Transverse|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 6
Testis|sQTL Liver|sQTL Lung|sQTL Stomach|sQTL Artery_Tibial|sQTL
Adrenal_Gland|sQTL
Number of selected tissue – G = 5
Testis|sQTL Liver|sQTL Lung|sQTL Stomach|sQTL
Artery_Tibial|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 3
Cells_Cultured_fibroblasts|sQTL Artery_Tibial|sQTL
Spleen|sQTL
Number of selected tissue – G = 10
Cells_Cultured_fibroblasts|sQTL Artery_Tibial|sQTL Spleen|sQTL
Adipose_Visceral_Omentum|sQTL Adrenal_Gland|sQTL Artery_Aorta|sQTL
Artery_Coronary|sQTL Brain_Caudate_basal_ganglia|sQTL
Brain_Cerebellar_Hemisphere|sQTL
Brain_Cerebellum|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 7
Artery_Tibial|sQTL Testis|sQTL Skin_Not_Sun_Exposed_Suprapubic|sQTL
Adipose_Visceral_Omentum|sQTL Heart_Atrial_Appendage|sQTL Lung|sQTL
Brain_Cerebellar_Hemisphere|sQTL
Number of selected tissue –
G = 7
Artery_Tibial|sQTL Testis|sQTL
Skin_Not_Sun_Exposed_Suprapubic|sQTL Adipose_Visceral_Omentum|sQTL
Heart_Atrial_Appendage|sQTL Lung|sQTL
Brain_Cerebellar_Hemisphere|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 4
Esophagus_Mucosa|sQTL Colon_Transverse|sQTL Whole_Blood|sQTL
Testis|sQTL
Number of selected tissue – G = 4
Esophagus_Mucosa|sQTL Colon_Transverse|sQTL Whole_Blood|sQTL
Testis|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 3
Cells_EBV-transformed_lymphocytes|sQTL Spleen|sQTL
Liver|sQTL
Number of selected tissue – G = 8
Cells_EBV-transformed_lymphocytes|sQTL Spleen|sQTL Liver|sQTL
Adipose_Subcutaneous|sQTL Breast_Mammary_Tissue|sQTL Nerve_Tibial|sQTL
Skin_Not_Sun_Exposed_Suprapubic|sQTL Thyroid|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 2
Brain_Nucleus_accumbens_basal_ganglia|sQTL
Vagina|sQTL
Number of selected tissue – G = 2
Brain_Nucleus_accumbens_basal_ganglia|sQTL
Vagina|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 6
Artery_Tibial|sQTL Spleen|sQTL Testis|sQTL Lung|sQTL
Breast_Mammary_Tissue|sQTL Colon_Sigmoid|sQTL
Number of
selected tissue – G = 5
Artery_Tibial|sQTL Spleen|sQTL Testis|sQTL
Lung|sQTL Breast_Mammary_Tissue|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 6
Cells_Cultured_fibroblasts|sQTL Testis|sQTL
Brain_Cerebellar_Hemisphere|sQTL Nerve_Tibial|sQTL
Brain_Hypothalamus|sQTL Heart_Left_Ventricle|sQTL
Number of
selected tissue – G = 6
Cells_Cultured_fibroblasts|sQTL Testis|sQTL
Brain_Cerebellar_Hemisphere|sQTL Nerve_Tibial|sQTL
Brain_Hypothalamus|sQTL Heart_Left_Ventricle|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 7
Artery_Aorta|sQTL Lung|sQTL Adrenal_Gland|sQTL Whole_Blood|sQTL
Breast_Mammary_Tissue|sQTL Cells_EBV-transformed_lymphocytes|sQTL
Nerve_Tibial|sQTL
Number of selected tissue – G = 7
Artery_Aorta|sQTL Lung|sQTL Adrenal_Gland|sQTL Whole_Blood|sQTL
Breast_Mammary_Tissue|sQTL Cells_EBV-transformed_lymphocytes|sQTL
Nerve_Tibial|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 7
Skin_Not_Sun_Exposed_Suprapubic|sQTL Whole_Blood|sQTL Spleen|sQTL
Testis|sQTL Brain_Frontal_Cortex_BA9|sQTL Nerve_Tibial|sQTL
Artery_Coronary|sQTL
Number of selected tissue – G = 7
Skin_Not_Sun_Exposed_Suprapubic|sQTL Whole_Blood|sQTL Spleen|sQTL
Testis|sQTL Brain_Frontal_Cortex_BA9|sQTL Nerve_Tibial|sQTL
Artery_Coronary|sQTL
[1] “p-value cutoff(0.05/num_tissue) =
0.00113636363636364”
Number of selected tissue – fisher = 7
Brain_Cerebellum|sQTL Testis|sQTL Pancreas|sQTL Whole_Blood|sQTL
Liver|sQTL Brain_Cerebellar_Hemisphere|sQTL
Adipose_Subcutaneous|sQTL
Number of selected tissue – G = 7
Brain_Cerebellum|sQTL Testis|sQTL Pancreas|sQTL Whole_Blood|sQTL
Liver|sQTL Brain_Cerebellar_Hemisphere|sQTL
Adipose_Subcutaneous|sQTL
colnames(converge_df) <- c("trait","num_EM_iter","converge")
cat("<br>")
DT::datatable(converge_df,caption = htmltools::tags$caption( style = 'caption-side: left; text-align: left; color:black; font-size:150% ;','EM convergence '),options = list(pageLength = 30) )
cat("<br>")
converge_df <- c()
for (trait in trait_psy){
param <- readRDS(paste0(folder_results,trait,"/",trait,".thin1.shared_all.param.RDS"))
gwas_n <- samplesize[trait]
param_summarized_fisher <- summarize_param(param = param,gwas_n = gwas_n,enrichment_test = "fisher",alternative = "greater")
param_summarized_G <- summarize_param(param = param,gwas_n = gwas_n,enrichment_test = "G")
param_df <- data.frame(
group = names(param_summarized_fisher$group_size),
group_size = as.numeric(param_summarized_fisher$group_size[names(param_summarized_fisher$group_size)]),
group_pve = as.numeric(param_summarized_fisher$group_pve[names(param_summarized_fisher$group_size)]),
prop_heritability = as.numeric(param_summarized_fisher$prop_heritability[names(param_summarized_fisher$group_size)]),
log_enrichment = as.numeric(param_summarized_fisher$log_enrichment[names(param_summarized_fisher$group_size)]),
log_enrichment_se = as.numeric(param_summarized_fisher$log_enrichment_se[names(param_summarized_fisher$group_size)]),
enrichment_pval_fisher = as.numeric(param_summarized_fisher$enrichment_pval[names(param_summarized_fisher$group_size)]),
enrichment_pval_G = as.numeric(param_summarized_G$enrichment_pval[names(param_summarized_G$group_size)])
)
param_df$total_pve <- param_summarized_fisher$total_pve
param_df$prop_heritability <- paste0(round(param_df$prop_heritability * 100, 5), "%")
param_df <- param_df[order(param_df$enrichment_pval_fisher,decreasing = F),]
param_df_qtl <- param_df[-nrow(param_df),]
threshold <- 0.05/(nrow(param_df_qtl)-1)
cat("<br>")
cat(knitr::knit_print(DT::datatable(param_df, caption = htmltools::tags$caption( style = 'caption-side: left; text-align: left; color:black; font-size:150% ;',trait,options = list(pageLength = 10)))))
cat("<br>")
cat("<br>")
cat("<br>")
print(paste0("p-value cutoff(0.05/num_tissue) = ",threshold))
cat("<br>")
cat("<br>")
cat(paste0("Number of selected tissue -- fisher = ",min(10,sum(param_df_qtl$enrichment_pval_fisher < threshold)),"\n"))
cat("<br>")
cat(paste0(
head(param_df_qtl$group[param_df_qtl$enrichment_pval_fisher < threshold], 10),
collapse = " "
))
cat("<br>")
cat("<br>")
cat("<br>")
cat(paste0("Number of selected tissue -- G = ",min(10,sum(param_df_qtl$enrichment_pval_G < threshold)),"\n"))
cat("<br>")
cat(paste0(
head(param_df_qtl$group[param_df_qtl$enrichment_pval_G < threshold], 10),
collapse = " "
))
cat("<br>")
cat("<br>")
cat("<br>")
EM_iter <- length(param$loglik_iters)
converge <- param$converged
converge_df <- rbind(converge_df,c(trait,EM_iter,converge))
}
[1] “p-value cutoff(0.05/num_tissue) = 0.00625”
Number of selected tissue – fisher = 2
Brain_Cerebellar_Hemisphere|sQTL
Brain_Cerebellum|sQTL
Number of selected tissue – G = 2
Brain_Cerebellar_Hemisphere|sQTL
Brain_Cerebellum|sQTL
[1] “p-value cutoff(0.05/num_tissue) = 0.00625”
Number of selected tissue – fisher = 3
Brain_Frontal_Cortex_BA9|sQTL Brain_Hypothalamus|sQTL
Brain_Caudate_basal_ganglia|sQTL
Number of selected tissue –
G = 3
Brain_Frontal_Cortex_BA9|sQTL Brain_Hypothalamus|sQTL
Brain_Caudate_basal_ganglia|sQTL
[1] “p-value cutoff(0.05/num_tissue) = 0.00625”
Number of selected tissue – fisher = 4
Brain_Cerebellum|sQTL
Brain_Cortex|sQTL Brain_Cerebellar_Hemisphere|sQTL
Brain_Putamen_basal_ganglia|sQTL
Number of selected tissue –
G = 4
Brain_Cerebellum|sQTL Brain_Cortex|sQTL
Brain_Cerebellar_Hemisphere|sQTL
Brain_Putamen_basal_ganglia|sQTL
[1] “p-value cutoff(0.05/num_tissue) = 0.00625”
Number of selected tissue – fisher = 2
Brain_Cerebellar_Hemisphere|sQTL
Brain_Cerebellum|sQTL
Number of selected tissue – G = 2
Brain_Cerebellar_Hemisphere|sQTL
Brain_Cerebellum|sQTL
[1] “p-value cutoff(0.05/num_tissue) = 0.00625”
Number of selected tissue – fisher = 3
Brain_Cerebellar_Hemisphere|sQTL
Brain_Nucleus_accumbens_basal_ganglia|sQTL
Brain_Cortex|sQTL
Number of selected tissue – G = 3
Brain_Cerebellar_Hemisphere|sQTL
Brain_Nucleus_accumbens_basal_ganglia|sQTL
Brain_Cortex|sQTL
[1] “p-value cutoff(0.05/num_tissue) = 0.00625”
Number of selected tissue – fisher = 1
Brain_Cerebellar_Hemisphere|sQTL
Number of selected
tissue – G = 1
Brain_Cerebellar_Hemisphere|sQTL
[1] “p-value cutoff(0.05/num_tissue) = 0.00625”
Number of selected tissue – fisher = 1
Brain_Cerebellar_Hemisphere|sQTL
Number of selected
tissue – G = 1
Brain_Cerebellar_Hemisphere|sQTL
colnames(converge_df) <- c("trait","num_EM_iter","converge")
cat("<br>")
DT::datatable(converge_df,caption = htmltools::tags$caption( style = 'caption-side: left; text-align: left; color:black; font-size:150% ;','EM convergence '),options = list(pageLength = 30) )
cat("<br>")
sessionInfo()
R version 4.2.0 (2022-04-22)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: CentOS Linux 7 (Core)
Matrix products: default
BLAS/LAPACK: /software/openblas-0.3.13-el7-x86_64/lib/libopenblas_haswellp-r0.3.13.so
locale:
[1] C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] ctwas_0.5.19
loaded via a namespace (and not attached):
[1] colorspace_2.0-3 rjson_0.2.21
[3] ellipsis_0.3.2 rprojroot_2.0.3
[5] XVector_0.36.0 locuszoomr_0.2.1
[7] GenomicRanges_1.48.0 base64enc_0.1-3
[9] fs_1.5.2 rstudioapi_0.13
[11] DT_0.22 ggrepel_0.9.1
[13] bit64_4.0.5 AnnotationDbi_1.58.0
[15] fansi_1.0.3 xml2_1.3.3
[17] codetools_0.2-18 logging_0.10-108
[19] cachem_1.0.6 knitr_1.39
[21] jsonlite_1.8.0 workflowr_1.7.0
[23] Rsamtools_2.12.0 dbplyr_2.1.1
[25] png_0.1-7 readr_2.1.2
[27] compiler_4.2.0 httr_1.4.3
[29] assertthat_0.2.1 Matrix_1.5-3
[31] fastmap_1.1.0 lazyeval_0.2.2
[33] cli_3.6.1 later_1.3.0
[35] htmltools_0.5.2 prettyunits_1.1.1
[37] tools_4.2.0 gtable_0.3.0
[39] glue_1.6.2 GenomeInfoDbData_1.2.8
[41] dplyr_1.1.4 rappdirs_0.3.3
[43] Rcpp_1.0.12 Biobase_2.56.0
[45] jquerylib_0.1.4 vctrs_0.6.5
[47] Biostrings_2.64.0 rtracklayer_1.56.0
[49] crosstalk_1.2.0 xfun_0.41
[51] stringr_1.5.1 irlba_2.3.5
[53] lifecycle_1.0.4 restfulr_0.0.14
[55] ensembldb_2.20.2 XML_3.99-0.14
[57] zlibbioc_1.42.0 zoo_1.8-10
[59] scales_1.3.0 gggrid_0.2-0
[61] hms_1.1.1 promises_1.2.0.1
[63] MatrixGenerics_1.8.0 ProtGenerics_1.28.0
[65] parallel_4.2.0 SummarizedExperiment_1.26.1
[67] AnnotationFilter_1.20.0 LDlinkR_1.2.3
[69] yaml_2.3.5 curl_4.3.2
[71] memoise_2.0.1 ggplot2_3.5.1
[73] sass_0.4.1 biomaRt_2.54.1
[75] stringi_1.7.6 RSQLite_2.3.1
[77] S4Vectors_0.34.0 BiocIO_1.6.0
[79] GenomicFeatures_1.48.3 BiocGenerics_0.42.0
[81] filelock_1.0.2 BiocParallel_1.30.3
[83] repr_1.1.4 GenomeInfoDb_1.39.9
[85] rlang_1.1.2 pkgconfig_2.0.3
[87] matrixStats_0.62.0 bitops_1.0-7
[89] evaluate_0.15 lattice_0.20-45
[91] purrr_1.0.2 GenomicAlignments_1.32.0
[93] htmlwidgets_1.5.4 cowplot_1.1.1
[95] bit_4.0.4 tidyselect_1.2.0
[97] magrittr_2.0.3 AMR_2.1.1
[99] R6_2.5.1 IRanges_2.30.0
[101] generics_0.1.2 DelayedArray_0.22.0
[103] DBI_1.2.2 pgenlibr_0.3.3
[105] pillar_1.9.0 KEGGREST_1.36.3
[107] RCurl_1.98-1.7 mixsqp_0.3-43
[109] tibble_3.2.1 crayon_1.5.1
[111] utf8_1.2.2 BiocFileCache_2.4.0
[113] plotly_4.10.0 tzdb_0.4.0
[115] rmarkdown_2.25 progress_1.2.2
[117] grid_4.2.0 data.table_1.14.2
[119] blob_1.2.3 git2r_0.30.1
[121] digest_0.6.29 tidyr_1.3.0
[123] httpuv_1.6.5 stats4_4.2.0
[125] munsell_0.5.0 viridisLite_0.4.0
[127] skimr_2.1.4 bslib_0.3.1