1 curatedCRCData: Clinically Annotated Data for the Colorectal Cancer Transcriptome
2 Data access and caching
3 Load data sets
4 Load datasets based on rules
5 Non-unique gene symbols
6 Appendix

1 curatedCRCData: Clinically Annotated Data for the Colorectal Cancer Transcriptome

This package represents a manually curated data collection for gene expression meta-analysis of patients with colorectal cancer. This resource provides uniformly prepared microarray data with curated and documented clinical metadata. It allows a computational user to efficiently identify studies and patient subgroups of interest for analysis and to run such analyses immediately without the challenges posed by harmonizing heterogeneous microarray technologies, study designs, expression data processing methods, and clinical data formats.

In this vignette, we give a short tour of the package and will show how to use it efficiently.

2 Data access and caching

As of version 2.46, the datasets are no longer stored inside the package: they are hosted on Zenodo and downloaded individually the first time they are requested, then cached locally with BiocFileCache so later uses need no network access. The cache lives in a package-specific directory, tools::R_user_dir("curatedCRCData", "cache"); to reclaim disk space, delete that directory or manage it with BiocFileCache.

The legacy data(TCGA.COAD_eset) syntax still works (it downloads through the same cache) but is deprecated and will be removed in a future release; please use the curatedCRCData() function shown below.

Throughout this vignette we set test = TRUE (and test.mode <- TRUE), which loads small offline subsets of each dataset that are bundled with the package, so that the vignette builds without downloading data. For real analyses, omit these settings to work with the full datasets.

3 Load data sets

Loading a single dataset is very easy. First we load the package:

library(curatedCRCData)

To get a listing of all the datasets, call curatedCRCData() with no arguments:

curatedCRCData()

##  [1] "GSE11237_eset"           "GSE12225.GPL3676_eset"  
##  [3] "GSE12945_eset"           "GSE13067_eset"          
##  [5] "GSE13294_eset"           "GSE14095_eset"          
##  [7] "GSE14333_eset"           "GSE16125.GPL5175_eset"  
##  [9] "GSE17536_eset"           "GSE17537_eset"          
## [11] "GSE17538.GPL570_eset"    "GSE18105_eset"          
## [13] "GSE2109_eset"            "GSE21510_eset"          
## [15] "GSE21815_eset"           "GSE24549.GPL5175_eset"  
## [17] "GSE24550.GPL5175_eset"   "GSE2630_eset"           
## [19] "GSE26682.GPL570_eset"    "GSE26682.GPL96_eset"    
## [21] "GSE26906_eset"           "GSE27544_eset"          
## [23] "GSE28702_eset"           "GSE3294_eset"           
## [25] "GSE33113_eset"           "GSE39582_eset"          
## [27] "GSE3964_eset"            "GSE4045_eset"           
## [29] "GSE4526_eset"            "GSE45270_eset"          
## [31] "TCGA.COAD_eset"          "TCGA.READ_eset"         
## [33] "TCGA.RNASeqV2_eset"      "TCGA.RNASeqV2.READ_eset"

Now to load a single dataset (drop test = TRUE to download the full dataset):

TCGA.COAD_eset <- curatedCRCData("TCGA.COAD_eset", test = TRUE)
TCGA.COAD_eset

## ExpressionSet (storageMode: lockedEnvironment)
## assayData: 202 features, 100 samples 
##   element names: exprs 
## protocolData: none
## phenoData
##   sampleNames: TCGA.AA.3520 TCGA.AA.3532 ... TCGA.AA.3984 (100 total)
##   varLabels: unique_patient_ID alt_sample_name ...
##     uncurated_author_metadata (59 total)
##   varMetadata: labelDescription
## featureData
##   featureNames: CXCL12 CXCR4 ... ACTR3 (202 total)
##   fvarLabels: probeset gene
##   fvarMetadata: labelDescription
## experimentData: use 'experimentData(object)'
##   pubMedIds: 22810696 
## Annotation: agilent-014850 whole human genome microarray 4x44k g4112f

The datasets are provided as Bioconductor ExpressionSet objects and we refer to the Bioconductor documentation for users unfamiliar with this data structure.

4 Load datasets based on rules

For a meta-analysis, we typically want to filter datasets and patients to get a population of patients we are interested in. We provide a short but powerful R script that does the filtering and provides the data as a list of ExpressionSet objects. One can use this script within R by first sourcing a config file which specifies the filters, like the minimum numbers of patients in each dataset. It is also possible to filter samples by annotation, for example to remove early stage and normal samples.

source(system.file("extdata",
"patientselection_all.config",package="curatedCRCData"))
test.mode <- TRUE  # use the bundled offline subsets in this vignette
ls()

## [1] "TCGA.COAD_eset"       "keep.common.only"     "meta.required"       
## [4] "min.number.of.events" "min.sample.size"      "quantile.cutoff"     
## [7] "rescale"              "strict.checking"      "test.mode"

See what the values of these variables we have loaded are. The variable names are fairly descriptive, but note that rule.1 is a character vector of length 2, where the first entry is the name of a clinical data variable, and the second entry is a Regular Expression providing a requirement for that variable. Any number of rules can be added, with increasing identifiers, e.g. rule.2, rule.3, etc.

Here strict.checking is FALSE, meaning that samples not annotated for the variables in these rules are allowed to pass the filter. If strict.checking == TRUE, samples missing this annotation will be removed.

sapply(ls(), get)

## $TCGA.COAD_eset
## ExpressionSet (storageMode: lockedEnvironment)
## assayData: 202 features, 100 samples 
##   element names: exprs 
## protocolData: none
## phenoData
##   sampleNames: TCGA.AA.3520 TCGA.AA.3532 ... TCGA.AA.3984 (100 total)
##   varLabels: unique_patient_ID alt_sample_name ...
##     uncurated_author_metadata (59 total)
##   varMetadata: labelDescription
## featureData
##   featureNames: CXCL12 CXCR4 ... ACTR3 (202 total)
##   fvarLabels: probeset gene
##   fvarMetadata: labelDescription
## experimentData: use 'experimentData(object)'
##   pubMedIds: 22810696 
## Annotation: agilent-014850 whole human genome microarray 4x44k g4112f 
## 
## $keep.common.only
## [1] FALSE
## 
## $meta.required
## NULL
## 
## $min.number.of.events
## [1] 0
## 
## $min.sample.size
## [1] 1
## 
## $quantile.cutoff
## [1] 0
## 
## $rescale
## [1] FALSE
## 
## $strict.checking
## [1] FALSE
## 
## $test.mode
## [1] TRUE

Now that we have defined the sample filter, we create a list of ExpressionSet objects by sourcing the createEsetList.R file:

source(system.file("extdata", "createEsetList.R", package = "curatedCRCData"))

## 2026-10-08 11:10:28.802576 INFO::Inside script createEsetList.R - inputArgs =
## 2026-10-08 11:10:28.814161 INFO::None provided
## 2026-10-08 11:10:28.879995 INFO::Loading curatedCRCData 2.45.6
## 2026-10-08 11:10:30.206691 INFO::Clean up the esets.
## 2026-10-08 11:10:30.30885 INFO::including GSE11237_eset
## 2026-10-08 11:10:30.321765 INFO::including GSE12225.GPL3676_eset
## 2026-10-08 11:10:30.332762 INFO::including GSE12945_eset
## 2026-10-08 11:10:30.34347 INFO::including GSE13067_eset
## 2026-10-08 11:10:30.86279 INFO::including GSE13294_eset
## 2026-10-08 11:10:30.873347 INFO::including GSE14095_eset
## 2026-10-08 11:10:30.882952 INFO::including GSE14333_eset
## 2026-10-08 11:10:30.892256 INFO::including GSE16125.GPL5175_eset
## 2026-10-08 11:10:30.901561 INFO::including GSE17536_eset
## 2026-10-08 11:10:30.910725 INFO::including GSE17537_eset
## 2026-10-08 11:10:30.919949 INFO::including GSE17538.GPL570_eset
## 2026-10-08 11:10:30.929193 INFO::including GSE18105_eset
## 2026-10-08 11:10:30.938405 INFO::including GSE2109_eset
## 2026-10-08 11:10:30.947631 INFO::including GSE21510_eset
## 2026-10-08 11:10:30.956864 INFO::including GSE21815_eset
## 2026-10-08 11:10:30.966064 INFO::including GSE24549.GPL5175_eset
## 2026-10-08 11:10:30.975178 INFO::including GSE24550.GPL5175_eset
## 2026-10-08 11:10:30.984134 INFO::including GSE2630_eset
## 2026-10-08 11:10:30.993222 INFO::including GSE26682.GPL570_eset
## 2026-10-08 11:10:31.002426 INFO::including GSE26682.GPL96_eset
## 2026-10-08 11:10:31.011607 INFO::including GSE26906_eset
## 2026-10-08 11:10:31.020606 INFO::including GSE27544_eset
## 2026-10-08 11:10:31.029634 INFO::including GSE28702_eset
## 2026-10-08 11:10:31.038749 INFO::including GSE3294_eset
## 2026-10-08 11:10:31.047953 INFO::including GSE33113_eset
## 2026-10-08 11:10:31.057213 INFO::including GSE39582_eset
## 2026-10-08 11:10:31.066363 INFO::including GSE3964_eset
## 2026-10-08 11:10:31.075468 INFO::including GSE4045_eset
## 2026-10-08 11:10:31.084462 INFO::including GSE4526_eset
## 2026-10-08 11:10:31.09334 INFO::including GSE45270_eset
## 2026-10-08 11:10:31.102497 INFO::including TCGA.COAD_eset
## 2026-10-08 11:10:31.111618 INFO::including TCGA.READ_eset
## 2026-10-08 11:10:31.120608 INFO::including TCGA.RNASeqV2.READ_eset
## 2026-10-08 11:10:31.12978 INFO::including TCGA.RNASeqV2_eset
## 2026-10-08 11:10:31.137265 INFO::Ids with missing data: GSE2630_eset, GSE3294_eset, TCGA.COAD_eset

It is also possible to run the script from the command line and then load the R data file within R:

R --vanilla "--args patientselection.config crc.eset.rda tmp.log"  < createEsetList.R

Now we have 34 datasets with samples that passed our filter in a list of ExpressionSet objects called esets:

names(esets)

##  [1] "GSE11237_eset"           "GSE12225.GPL3676_eset"  
##  [3] "GSE12945_eset"           "GSE13067_eset"          
##  [5] "GSE13294_eset"           "GSE14095_eset"          
##  [7] "GSE14333_eset"           "GSE16125.GPL5175_eset"  
##  [9] "GSE17536_eset"           "GSE17537_eset"          
## [11] "GSE17538.GPL570_eset"    "GSE18105_eset"          
## [13] "GSE2109_eset"            "GSE21510_eset"          
## [15] "GSE21815_eset"           "GSE24549.GPL5175_eset"  
## [17] "GSE24550.GPL5175_eset"   "GSE2630_eset"           
## [19] "GSE26682.GPL570_eset"    "GSE26682.GPL96_eset"    
## [21] "GSE26906_eset"           "GSE27544_eset"          
## [23] "GSE28702_eset"           "GSE3294_eset"           
## [25] "GSE33113_eset"           "GSE39582_eset"          
## [27] "GSE3964_eset"            "GSE4045_eset"           
## [29] "GSE4526_eset"            "GSE45270_eset"          
## [31] "TCGA.COAD_eset"          "TCGA.READ_eset"         
## [33] "TCGA.RNASeqV2.READ_eset" "TCGA.RNASeqV2_eset"

5 Non-unique gene symbols

In the standard version of curatedCRCData (the version available on Bioconductor), we collapse manufacturer probesets to official HGNC symbols using the Biomart database. Some probesets are mapped to multiple HGNC symbols in this database. For these probesets, we provide all the symbols. For example 220159_at maps to ABCA11P and ZNF721 and we provide ABCA11P///ZNF721 as probeset name. If you have an array of gene symbols for which you want to access the expression data, “ABCA11P” would not be found in curatedCRCData in this example. The following function will create a new ExpressionSet in which both ZNF721 and ABCA11P are features with identical expression data:

expandProbesets <- function (eset, sep = "///") 
{
    x <- lapply(featureNames(eset), function(x) strsplit(x, sep)[[1]])
    eset <- eset[order(sapply(x, length)), ]
    x <- lapply(featureNames(eset), function(x) strsplit(x, sep)[[1]])
    idx <- unlist(sapply(1:length(x), function(i) rep(i, length(x[[i]]))))
    xx <- !duplicated(unlist(x))
    idx <- idx[xx]
    x <- unlist(x)[xx]
    eset <- eset[idx, ]
    featureNames(eset) <- x
    eset
}

X <- TCGA.COAD_eset[head(grep("AA", featureNames(TCGA.COAD_eset))),]
exprs(X)[,1:3]

##         TCGA.AA.3520 TCGA.AA.3532 TCGA.AA.3553
## AAAS        -0.72125     -1.51150     -1.01250
## AACS         0.02225      0.82375     -0.08500
## AADAC        0.02775     -0.42900      1.12525
## AADACL1      1.06600      1.85550      0.92800
## AADACL2      0.08750     -0.61825     -0.47525
## AADACL3      0.38100      0.31100      0.33950

exprs(expandProbesets(X))[,1:3]

##         TCGA.AA.3520 TCGA.AA.3532 TCGA.AA.3553
## AAAS        -0.72125     -1.51150     -1.01250
## AACS         0.02225      0.82375     -0.08500
## AADAC        0.02775     -0.42900      1.12525
## AADACL1      1.06600      1.85550      0.92800
## AADACL2      0.08750     -0.61825     -0.47525
## AADACL3      0.38100      0.31100      0.33950

6 Appendix

6.1 Available Clinical Characteristics

Available clinical annotation. This heatmap visualizes for each curated clinical characteristic (rows) the availability in each dataset (columns). Red indicates that the corresponding characteristic is available for at least one sample in the dataset.

Figure 1: Available clinical annotation
This heatmap visualizes for each curated clinical characteristic (rows) the availability in each dataset (columns). Red indicates that the corresponding characteristic is available for at least one sample in the dataset.

6.2 Summarizing the List of ExpressionSets

This example provides a table summarizing the datasets being used, and is useful when publishing analyses based on curatedCRCData. First, define some useful functions for this purpose:

source(system.file("extdata", "summarizeEsets.R", package = "curatedCRCData"))

## Warning in min(which(km.fit$surv < 0.5)): no non-missing arguments to min;
## returning Inf
## Warning in min(which(km.fit$surv < 0.5)): no non-missing arguments to min;
## returning Inf

## Warning in min(which(reverse.km.fit$surv < 0.5)): no non-missing arguments to
## min; returning Inf
## Warning in min(which(reverse.km.fit$surv < 0.5)): no non-missing arguments to
## min; returning Inf
## Warning in min(which(reverse.km.fit$surv < 0.5)): no non-missing arguments to
## min; returning Inf

Optionally write this table to file, for example ( replace myfile <- tempfile() with something like myfile <- "nicetable.csv" )

(myfile <- tempfile())

## [1] "/tmp/RtmpjdwtYB/file3b6f515e9e02e2"

write.table(summary.table, file=myfile, row.names=FALSE, quote=TRUE, sep=",")

Table 1: Datasets provided by curatedCRCData.
	Study	PMID	N samples	msi status	G	Platform	median.survival	median follow-up	percent censoring	binarized OS (long/short)
GSE11237	Auman, Mcleod 2008	18653328	23	0/0/23	3/16/4/0/0	Affymetrix HG_U95Av2	NA	NA	NA	NA
GSE12225.GPL3676	Lips, Morreau 2008	18959792	42	0/0/42	0/0/0/0/42	NA	NA	NA	NA	NA
GSE12945	Staub, Rosenthal 2009	19399471	62	0/0/62	0/31/31/0/0	Affymetrix HG-U133A	NA	49	81	NA
GSE13067	Jorissen and Sieber 2008	19088021	74	0/0/74	0/0/0/0/74	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE13294	Jorissen and Sieber 2008	19088021	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE14095	Watanabe, Hashimoto 2008	21680303	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE14333	Jorissen and Sieber 2008	19996206	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE16125.GPL5175	Reid, Pierotti 2009	19672874	36	0/0/36	0/0/0/0/36	Affymetrix HuEx-1_0-st	74	22	69	NA
GSE17536	Smith JJ,??Beauchamp RD 2009	19914252	100	0/0/100	13/79/8/0/0	Affymetrix HG-U133Plus2	133	65	73	NA
GSE17537	Smith JJ,??Beauchamp RD 2009	19914252	55	0/0/55	1/32/3/0/19	Affymetrix HG-U133Plus2	NA	57	64	NA
GSE17538.GPL570	Smith JJ,??Beauchamp RD 2009	19914252	100	0/0/100	13/79/8/0/0	Affymetrix HG-U133Plus2	133	65	73	NA
GSE18105	Matsuyama, Sugihara 2009	20162577	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE2109	expO, IGC 2005	PMID unknown	100	0/0/100	2/64/19/2/13	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE21510	Tsukamoto, Sugihara 2010	21270110	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE21815	Mori M,??Mimori K,??Yokobori T 2010	21862635	100	0/0/100	22/14/1/0/63	Agilent G4112F	NA	NA	NA	NA
GSE24549.GPL5175	Sveen A,????esen TH,??Rognum TO,??Lothe RA,??Skotheim RI 2011	21619627	83	0/0/83	0/0/0/0/83	Affymetrix HuEx-1_0-st	NA	NA	NA	NA
GSE24550.GPL5175	Sveen A,????esen TH,??Rognum TO,??Lothe RA,??Skotheim RI 2011	21619627	90	0/0/90	0/0/0/0/90	Affymetrix HuEx-1_0-st	NA	NA	NA	NA
GSE2630	Bandr??E,??Malumbres R,??Cubedo E,??Sola J,??Garc??Foncillas J,??Labarga A 2005	17390049	16	0/0/16	0/0/0/0/16	NA	NA	NA	NA	NA
GSE26682.GPL570	Vilar E,??Morgan MA 2011	21300766	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE26682.GPL96	Vilar E,??Morgan MA 2011	21300766	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133A	NA	NA	NA	NA
GSE26906	Olschwang S 2011	22496922	90	0/0/90	0/0/0/0/90	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE27544	Bernal M,??Garc??Alcalde F,??Concha ????Blanco A,??Garrido F,??Ruiz-Cabello F 2011	PMID unknown	22	0/0/22	0/0/0/0/22	Affymetrix HT HG-U133+ PM	NA	NA	NA	NA
GSE28702	Tsuji 2011	22095227	83	0/0/83	62/16/5/0/0	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE3294	Bianchini 2005	16773188	24	0/0/24	10/11/3/0/0	UHN SS-Human 19Kv7	NA	NA	NA	NA
GSE33113	Medema JP,??Tanis PJ 2011	22496204	96	0/0/96	0/0/0/0/96	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE39582	Marisa, Boige 2012	23700391	100	0/0/100	0/0/0/0/100	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE3964	Graudens, Imbeaud 2006	16542501	29	0/0/29	0/0/0/0/29	NA	NA	NA	NA	NA
GSE4045	Laiho, Aaltonen 2007	16819509	37	0/0/37	4/28/4/0/1	Affymetrix HG-U133A	NA	NA	NA	NA
GSE4526	Watanabe T,??Kobunai T,??Toda E,??Oka T 2006	19016304	36	0/0/36	0/0/0/0/36	Affymetrix HG-U133Plus2	NA	NA	NA	NA
GSE45270	Medema JP,??de Sousa E Melo F,??Vermeulen L,??Jansen M,??Dekker E,??Van Noesel C,??Fessler E 2013	PMID unknown	13	0/0/13	0/0/0/0/13	Affymetrix HG-U133Plus2	NA	NA	NA	NA
TCGA.COAD	The Cancer Genome Atlas Network 2012	22810696	100	0/0/100	0/0/0/0/100	Agilent G4502A-07-3	24	25	33	NA
TCGA.READ	The Cancer Genome Atlas Network 2012	22810696	51	0/0/51	0/0/0/0/51	Agilent G4502A-07-3	10	NA	0	NA
TCGA.RNASeqV2.READ	The Cancer Genome Atlas Network 2012	22810696	6	0/0/6	0/0/0/0/6		41	NA	0	NA
TCGA.RNASeqV2	The Cancer Genome Atlas Network 2012	22810696	100	0/0/100	0/0/0/0/100		14	NA	15	NA

6.3 For non-R users

If you are not doing your analysis in R, and just want to get some data you have identified from the curatedCRCData manual, here is a simple way to do it. For one dataset:

library(curatedCRCData)
library(Biobase)
TCGA.COAD_eset <- curatedCRCData("TCGA.COAD_eset")
write.csv(exprs(TCGA.COAD_eset), file="TCGA.COAD_eset_exprs.csv")
write.csv(pData(TCGA.COAD_eset), file="TCGA.COAD_eset_clindata.csv")

Or for several datasets:

data.to.fetch <- curatedCRCData(c("TCGA.COAD_eset", "GSE39582_eset"))
for (onedata in names(data.to.fetch)){
    write.csv(exprs(data.to.fetch[[onedata]]),
              file=paste(onedata, "_exprs.csv", sep=""))
    write.csv(pData(data.to.fetch[[onedata]]),
              file=paste(onedata, "_clindata.csv", sep=""))
}

6.4 Session Info

## R version 4.6.1 (2026-06-24)
## Platform: x86_64-pc-linux-gnu
## Running under: Ubuntu 24.04.5 LTS
## 
## Matrix products: default
## BLAS:   /home/biocbuild/bbs-3.24-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] knitr_1.52            logging_0.10-111      survival_3.8-12      
##  [4] curatedCRCData_2.45.6 Biobase_2.73.2        BiocGenerics_0.59.12 
##  [7] generics_0.1.4        xtable_1.8-8          sva_3.61.0           
## [10] BiocParallel_1.47.0   genefilter_1.95.0     mgcv_1.9-4           
## [13] nlme_3.1-171          BiocStyle_2.41.0     
## 
## loaded via a namespace (and not attached):
##  [1] KEGGREST_1.53.6       httr2_1.3.0           xfun_0.61            
##  [4] bslib_0.12.0          lattice_0.23-1        vctrs_0.7.3          
##  [7] tools_4.6.1           curl_8.0.0            stats4_4.6.1         
## [10] parallel_4.6.1        tibble_3.3.1          AnnotationDbi_1.75.2 
## [13] RSQLite_3.53.3        blob_1.3.0            pkgconfig_2.0.3      
## [16] BiocBaseUtils_1.15.1  Matrix_1.7-6          dbplyr_2.6.0         
## [19] S4Vectors_0.51.10     lifecycle_1.0.5       compiler_4.6.1       
## [22] Biostrings_2.81.9     tinytex_0.61          statmod_1.5.2        
## [25] Seqinfo_1.3.2         codetools_0.2-20      htmltools_0.5.9      
## [28] sass_0.4.10           yaml_2.3.12           pillar_1.11.1        
## [31] crayon_1.5.3          jquerylib_0.1.4       cachem_1.1.0         
## [34] limma_3.99.0          magick_2.9.1          tidyselect_1.2.1     
## [37] locfit_1.5-9.12       digest_0.6.39         dplyr_1.2.1          
## [40] bookdown_0.48         splines_4.6.1         fastmap_1.2.0        
## [43] grid_4.6.1            cli_3.6.6             magrittr_2.0.5       
## [46] XML_3.99-0.25         edgeR_4.99.6          filelock_1.0.3       
## [49] bit64_4.8.6           rmarkdown_2.32        XVector_0.53.0       
## [52] httr_1.4.9            matrixStats_1.5.0     bit_4.6.0            
## [55] otel_0.2.0            png_0.1-9             memoise_2.0.1        
## [58] evaluate_1.0.5        IRanges_2.47.5        BiocFileCache_3.3.0  
## [61] rlang_1.3.0           Rcpp_1.1.2            glue_1.8.1           
## [64] DBI_1.3.0             BiocManager_1.30.27   annotate_1.91.0      
## [67] jsonlite_2.0.0        R6_2.6.1              MatrixGenerics_1.25.0

curatedCRCData: Clinically Annotated Data for the Colorectal Cancer Transcriptome

2013

Contents