By default, CaDrA
performs both forward and backward search algorithm to look for a subset
of features whose union is maximally associated with an outcome of
interest, based on (currently) one of four scoring functions
(Kolmogorov-Smirnov, Conditional Mutual
Information, Wilcoxon, and
custom-defined). To test whether the strength of the
association between the set of features and the observed input scores
(e.g., pathway activity, drug sensitivity, etc.) is greater than it
would be expected by chance, CaDrA supports
permutation-based significance testing. Importantly, the permutation
test iterates over the entire search procedure (e.g., if
top_N = 7
, each permutation iteration will consist of
running the search over the top 7 features).
binary features matrix
also known as
Feature Set
(such as somatic mutations, copy number
alterations, chromosomal translocations, etc.) The 1/0 row vectors
indicate the presence/absence of ‘omics’ features in the samples. The
Feature Set
can be a matrix or an object of class
SummarizedExperiment from
SummarizedExperiment package)Input Scores
)
representing a functional response of interest (such as protein
expression, pathway activity, etc.)Here we are using Kolmogorow-Smirnow (KS) scoring method to search for best features
candidate_search_res <- CaDrA::candidate_search(
FS = sim_FS,
input_score = sim_Scores,
method = "ks_pval", # Use Kolmogorow-Smirnow scoring function
method_alternative = "less", # Use one-sided hypothesis testing
weights = NULL, # If weights is provided, perform a weighted-KS test
search_method = "both", # Apply both forward and backward search
top_N = 7, # Number of top features to kick start the search
max_size = 10, # Allow at most 10 features in meta-feature matrix
best_score_only = FALSE # Return all results from the search
)
# Set seed for permutation-based testing
set.seed(123)
perm_res <- CaDrA::CaDrA(
FS = sim_FS,
input_score = sim_Scores,
method = "ks_pval", # Use Kolmogorow-Smirnow scoring function
method_alternative = "less", # Use one-sided hypothesis testing
weights = NULL, # If weights is provided, perform a weighted-KS test
search_method = "both", # Apply both forward and backward search
top_N = 7, # Repeat the search with the top N features
max_size = 10, # Allow at most 10 features in the meta-feature matrix
n_perm = 100, # Number of permutations to perform
perm_alternative = "one.sided", # One-sided permutation-based p-value alternative type
plot = FALSE, # We will plot later
ncores = 2 # Number of cores to perform parallelization
)
sessionInfo()
R version 4.4.2 (2024-10-31)
Platform: x86_64-pc-linux-gnu
Running under: Ubuntu 24.04.1 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] stats graphics grDevices utils datasets methods base
other attached packages:
[1] CaDrA_1.5.0 testthat_3.2.1.1 devtools_2.4.5 usethis_3.1.0
[5] rmarkdown_2.29
loaded via a namespace (and not attached):
[1] bitops_1.0-9 tcltk_4.4.2
[3] remotes_2.5.0 rlang_1.1.4
[5] magrittr_2.0.3 matrixStats_1.4.1
[7] compiler_4.4.2 vctrs_0.6.5
[9] reshape2_1.4.4 stringr_1.5.1
[11] profvis_0.4.0 pkgconfig_2.0.3
[13] crayon_1.5.3 fastmap_1.2.0
[15] XVector_0.47.0 ellipsis_0.3.2
[17] labeling_0.4.3 caTools_1.18.3
[19] utf8_1.2.4 promises_1.3.2
[21] sessioninfo_1.2.2 UCSC.utils_1.3.0
[23] purrr_1.0.2 xfun_0.49
[25] zlibbioc_1.52.0 cachem_1.1.0
[27] GenomeInfoDb_1.43.2 jsonlite_1.8.9
[29] later_1.4.1 DelayedArray_0.33.2
[31] parallel_4.4.2 R6_2.5.1
[33] bslib_0.8.0 stringi_1.8.4
[35] pkgload_1.4.0 brio_1.1.5
[37] GenomicRanges_1.59.1 jquerylib_0.1.4
[39] Rcpp_1.0.13-1 SummarizedExperiment_1.37.0
[41] iterators_1.0.14 knitr_1.49
[43] R.utils_2.12.3 IRanges_2.41.1
[45] httpuv_1.6.15 Matrix_1.7-1
[47] R.cache_0.16.0 rstudioapi_0.17.1
[49] abind_1.4-8 yaml_2.3.10
[51] doParallel_1.0.17 gplots_3.2.0
[53] codetools_0.2-20 miniUI_0.1.1.1
[55] misc3d_0.9-1 pkgbuild_1.4.5
[57] lattice_0.22-6 tibble_3.2.1
[59] plyr_1.8.9 shiny_1.9.1
[61] Biobase_2.67.0 withr_3.0.2
[63] evaluate_1.0.1 desc_1.4.3
[65] urlchecker_1.0.1 pillar_1.9.0
[67] MatrixGenerics_1.19.0 KernSmooth_2.23-24
[69] foreach_1.5.2 stats4_4.4.2
[71] generics_0.1.3 rprojroot_2.0.4
[73] S4Vectors_0.45.2 ggplot2_3.5.1
[75] munsell_0.5.1 scales_1.3.0
[77] gtools_3.9.5 xtable_1.8-4
[79] glue_1.8.0 ppcor_1.1
[81] maketools_1.3.1 tools_4.4.2
[83] sys_3.4.3 buildtools_1.0.0
[85] fs_1.6.5 grid_4.4.2
[87] knnmi_1.0 colorspace_2.1-1
[89] GenomeInfoDbData_1.2.13 cli_3.6.3
[91] fansi_1.0.6 S4Arrays_1.7.1
[93] gtable_0.3.6 R.methodsS3_1.8.2
[95] sass_0.4.9 digest_0.6.37
[97] BiocGenerics_0.53.3 SparseArray_1.7.2
[99] farver_2.1.2 htmlwidgets_1.6.4
[101] memoise_2.0.1 htmltools_0.5.8.1
[103] R.oo_1.27.0 lifecycle_1.0.4
[105] httr_1.4.7 mime_0.12
[107] MASS_7.3-61