library(dplyr)
library(ggplot2)
library(survival)
library(futile.logger)
library(curatedTCGAData)
library(TCGAutils)
library(MultiAssayExperiment)
#
library(glmSparseNet)
#
# Some general options for futile.logger the debugging package
flog.layout(layout.format("[~l] ~m"))
options(
"glmSparseNet.show_message" = FALSE,
"glmSparseNet.base_dir" = withr::local_tempdir()
)
# Setting ggplot2 default theme as minimal
theme_set(ggplot2::theme_minimal())The data is loaded from an online curated dataset downloaded from
TCGA using curatedTCGAData bioconductor package and
processed.
To accelerate the process we use a very reduced dataset down to around 100 variables only (genes), which is stored as a data object in this package. However, the procedure to obtain the data manually is described in the following chunk.
prad <- curatedTCGAData(
diseaseCode = "PRAD", assays = "RNASeq2GeneNorm",
version = "1.1.38", dry.run = FALSE
)Build the survival data from the clinical columns.
xdata and
ydata# keep only solid tumour (code: 01)
pradPrimarySolidTumor <- TCGAutils::TCGAsplitAssays(prad, "01")
xdataRaw <- t(assay(pradPrimarySolidTumor[[1]]))
# Get survival information
ydataRaw <- colData(pradPrimarySolidTumor) |>
as.data.frame() |>
# Find max time between all days (ignoring missings)
dplyr::rowwise() |>
dplyr::mutate(
time = max(days_to_last_followup, days_to_death, na.rm = TRUE)
) |>
# Keep only survival variables and codes
dplyr::select(patientID, status = vital_status, time) |>
# Discard individuals with survival time less or equal to 0
dplyr::filter(!is.na(time) & time > 0) |>
as.data.frame()
# Set index as the patientID
rownames(ydataRaw) <- ydataRaw$patientID
# keep only features that have standard deviation > 0
xdataRaw <- xdataRaw[
TCGAbarcode(rownames(xdataRaw)) %in% rownames(ydataRaw),
]
xdataRaw <- xdataRaw[, apply(xdataRaw, 2, sd) != 0] |>
scale()
# Order ydata the same as assay
ydataRaw <- ydataRaw[TCGAbarcode(rownames(xdataRaw)), ]
set.seed(params$seed)
smallSubset <- c(
geneNames(c(
"ENSG00000103091", "ENSG00000064787",
"ENSG00000119915", "ENSG00000120158",
"ENSG00000114491", "ENSG00000204176",
"ENSG00000138399"
))$external_gene_name,
sample(colnames(xdataRaw), 100)
) |>
unique() |>
sort()
xdata <- xdataRaw[, smallSubset[smallSubset %in% colnames(xdataRaw)]]
ydata <- ydataRaw |> dplyr::select(time, status)Fit model model penalizing by the hubs using the cross-validation
function by cv.glmHub.
Shows the results of 100 different parameters used to
find the optimal value in 10-fold cross-validation. The two vertical
dotted lines represent the best model and a model with less variables
selected (genes), but within a standard error distance from the
best.
Taking the best model described by lambda.min
coefsCV <- Filter(function(.x) .x != 0, coef(fitted, s = "lambda.min")[, 1])
data.frame(
ensembl.id = names(coefsCV),
gene.name = geneNames(names(coefsCV))$external_gene_name,
coefficient = coefsCV,
stringsAsFactors = FALSE
) |>
arrange(gene.name) |>
knitr::kable()| ensembl.id | gene.name | coefficient | |
|---|---|---|---|
| AKAP9 | AKAP9 | AKAP9 | 0.2627933 |
| ALPK2 | ALPK2 | ALPK2 | -0.0738446 |
| ATP5G2 | ATP5G2 | ATP5G2 | -0.2585744 |
| C22orf32 | C22orf32 | C22orf32 | -0.2126287 |
| CSNK2A1P | CSNK2A1P | CSNK2A1P | -1.4902722 |
| MYST3 | MYST3 | MYST3 | -1.6228029 |
| NBPF10 | NBPF10 | NBPF10 | 0.4525259 |
| PFN1 | PFN1 | PFN1 | 0.4196058 |
| SCGB2A2 | SCGB2A2 | SCGB2A2 | 0.0745791 |
| SLC25A1 | SLC25A1 | SLC25A1 | -0.8526360 |
| STX4 | STX4 | STX4 | -0.1695387 |
| SYP | SYP | SYP | 0.2530633 |
| TMEM141 | TMEM141 | TMEM141 | -0.8307072 |
| UMPS | UMPS | UMPS | 0.2252967 |
| ZBTB26 | ZBTB26 | ZBTB26 | 0.3699276 |
separate2GroupsCox(as.vector(coefsCV),
xdata[, names(coefsCV)],
ydata,
plotTitle = "Full dataset", legendOutside = FALSE
)## $pvalue
## [1] 0.001155155
##
## $plot
##
## $km
## Call: survfit(formula = survival::Surv(time, status) ~ group, data = prognosticIndexDf)
##
## n events median 0.95LCL 0.95UCL
## Low risk - 1 249 0 NA NA NA
## High risk - 1 248 10 3502 3467 NA
## R version 4.5.2 (2025-10-31)
## Platform: x86_64-pc-linux-gnu
## Running under: Ubuntu 24.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
## LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/libopenblasp-r0.3.26.so; LAPACK version 3.12.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 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: Etc/UTC
## tzcode source: system (glibc)
##
## attached base packages:
## [1] grid parallel stats4 stats graphics grDevices utils
## [8] datasets methods base
##
## other attached packages:
## [1] glmnet_4.1-10 VennDiagram_1.8.2
## [3] reshape2_1.4.5 forcats_1.0.1
## [5] Matrix_1.7-4 glmSparseNet_1.29.0
## [7] TCGAutils_1.31.4 curatedTCGAData_1.33.1
## [9] MultiAssayExperiment_1.37.2 SummarizedExperiment_1.41.1
## [11] Biobase_2.71.0 GenomicRanges_1.63.1
## [13] Seqinfo_1.1.0 IRanges_2.45.0
## [15] S4Vectors_0.49.0 BiocGenerics_0.57.0
## [17] generics_0.1.4 MatrixGenerics_1.23.0
## [19] matrixStats_1.5.0 futile.logger_1.4.9
## [21] survival_3.8-6 ggplot2_4.0.2
## [23] dplyr_1.2.0 BiocStyle_2.39.0
##
## loaded via a namespace (and not attached):
## [1] RColorBrewer_1.1-3 sys_3.4.3
## [3] jsonlite_2.0.0 shape_1.4.6.1
## [5] magrittr_2.0.4 GenomicFeatures_1.63.1
## [7] farver_2.1.2 rmarkdown_2.30
## [9] BiocIO_1.21.0 vctrs_0.7.1
## [11] memoise_2.0.1 Rsamtools_2.27.1
## [13] RCurl_1.98-1.17 rstatix_0.7.3
## [15] htmltools_0.5.9 S4Arrays_1.11.1
## [17] BiocBaseUtils_1.13.0 progress_1.2.3
## [19] AnnotationHub_4.1.0 lambda.r_1.2.4
## [21] curl_7.0.0 broom_1.0.12
## [23] Formula_1.2-5 SparseArray_1.11.11
## [25] pROC_1.19.0.1 sass_0.4.10
## [27] bslib_0.10.0 plyr_1.8.9
## [29] httr2_1.2.2 futile.options_1.0.1
## [31] cachem_1.1.0 buildtools_1.0.0
## [33] GenomicAlignments_1.47.0 lifecycle_1.0.5
## [35] iterators_1.0.14 pkgconfig_2.0.3
## [37] R6_2.6.1 fastmap_1.2.0
## [39] digest_0.6.39 AnnotationDbi_1.73.0
## [41] ExperimentHub_3.1.0 RSQLite_2.4.6
## [43] ggpubr_0.6.3 filelock_1.0.3
## [45] labeling_0.4.3 httr_1.4.8
## [47] abind_1.4-8 compiler_4.5.2
## [49] bit64_4.6.0-1 withr_3.0.2
## [51] S7_0.2.1 backports_1.5.0
## [53] BiocParallel_1.45.0 carData_3.0-6
## [55] DBI_1.3.0 ggsignif_0.6.4
## [57] biomaRt_2.67.6 rappdirs_0.3.4
## [59] DelayedArray_0.37.0 rjson_0.2.23
## [61] tools_4.5.2 glue_1.8.0
## [63] restfulr_0.0.16 checkmate_2.3.4
## [65] gtable_0.3.6 tzdb_0.5.0
## [67] tidyr_1.3.2 survminer_0.5.2
## [69] hms_1.1.4 car_3.1-5
## [71] xml2_1.5.2 XVector_0.51.0
## [73] BiocVersion_3.23.1 foreach_1.5.2
## [75] pillar_1.11.1 stringr_1.6.0
## [77] splines_4.5.2 BiocFileCache_3.1.0
## [79] lattice_0.22-9 rtracklayer_1.71.3
## [81] bit_4.6.0 tidyselect_1.2.1
## [83] maketools_1.3.2 Biostrings_2.79.5
## [85] knitr_1.51 gridExtra_2.3
## [87] xfun_0.56 stringi_1.8.7
## [89] UCSC.utils_1.7.1 yaml_2.3.12
## [91] evaluate_1.0.5 codetools_0.2-20
## [93] cigarillo_1.1.0 tibble_3.3.1
## [95] BiocManager_1.30.27 cli_3.6.5
## [97] jquerylib_0.1.4 Rcpp_1.1.1
## [99] GenomeInfoDb_1.47.2 GenomicDataCommons_1.35.1
## [101] dbplyr_2.5.2 png_0.1-9
## [103] XML_3.99-0.22 readr_2.2.0
## [105] blob_1.3.0 prettyunits_1.2.0
## [107] bitops_1.0-9 scales_1.4.0
## [109] purrr_1.2.1 crayon_1.5.3
## [111] rlang_1.1.7 KEGGREST_1.51.1
## [113] rvest_1.0.5 formatR_1.14