A Curated Microarrays Dataset of MDI-induced Differentiated Adipocytes (3T3-L1) Under Genetic and Pharmacological Perturbations
A curated dataset of Microarrays samples. The samples are MDI-induced pre- adipocytes (3T3-L1) at different time points/stage of differentiation under different types of genetic (knockdown/overexpression) and pharmacological (drug treatment) perturbations. The package documents the data collection and processing. In addition to the documentation, the package contains the scripts that was used to generated the data.
This package is for documenting and distributing a curated dataset of gene expression from MDI-induced 3T3-L1 adipocyte cell model under genetic and pharmacological modification.
The package contains two things:
The data contained in the package can be used in any number of downstream analysis such as differential expression and gene set enrichment.
curatedAdipoArray package can be installed from Bioconductor using
The pre-processing and processing of the data setup environment is available as a
docker image. This image is also suitable for reproducing this document. The
docker image can be obtained using the
docker CLI client.
$ docker pull bcmslab/adiporeg_array:latest
We surveyed the literature for MDI-induced 3T3-L1 microarrays studies with or without course perturbations. 43 published studies were included. 47 datasets from these studies were examined for metadata and annotation completeness. One and two studies were excluded for missing probe intensities and probe annotations respectively. In addition to the data and the metadata, the original publications were also examined to extract the experimental design and other missing experimental details. The remaining datasets were curated, cleaned and packaged in two final datasets for each type of differentiation course perturbation.
The probe intensities, probe annotation and metadata of each study were obtained from the gene expression omnibus (GEO) using
GEOquery. The probe intensities (expression matrices) were collapsed using probe to gene symbol annotation using
collapsRows. The metadata for studies, data series and samples were homogenized across studies using common vocabularies to describe the experimental designs. Information for each sample of the differentiation status and time point were retrieved and recorded. In addition, the treatment type, target, dose and time were added for each sample. The processed datasets were packaged in
Bioconductor``SummarizedExperiment object individually.
For illustration purposes, the dataset objects were merged into two separate
SummarizedExperiment for the genetic or the pharmacological perturbations. In each set, missing and low intensity genes were removed. Then the gene intensities were log transformed and normalized across studies using
limma. Finally, the known batch effects (data series and platform) were removed using
# query package resources on ExperimentHub eh <- ExperimentHub() query(eh, "curatedAdipoArray") #> ExperimentHub with 45 records #> # snapshotDate(): 2023-10-24 #> # $dataprovider: GEO #> # $species: Mus musculus #> # $rdataclass: SummarizedExperiment #> # additional mcols(): taxonomyid, genome, description, #> # coordinate_1_based, maintainer, rdatadateadded, preparerclass, tags, #> # rdatapath, sourceurl, sourcetype #> # retrieve records with, e.g., 'object[["EH3245"]]' #> #> title #> EH3245 | A Clean Expression Matrix of the GEOGSE102403 Dataset. #> EH3246 | A Clean Expression Matrix of the GEOGSE122054 Dataset. #> EH3247 | A Clean Expression Matrix of the GEOGSE12929 Dataset. #> EH3248 | A Clean Expression Matrix of the GEOGSE14004 Dataset. #> EH3249 | A Clean Expression Matrix of the GEOGSE1458 Dataset. #> ... ... #> EH3285 | A Clean Expression Matrix of the GEOGSE97241 Dataset. #> EH3286 | A Curated Microarrays Dataset of MDI-induced Differentiated Adi... #> EH3287 | A Curated Microarrays Dataset (processed) of MDI-induced Differe... #> EH3288 | A Curated Microarrays Dataset of MDI-induced Differentiated Adi... #> EH3289 | A Curated Microarrays Dataset (processed) of MDI-induced Differe...
Each of the objects attached to this package is an
SummarizedExperiment. This object contains two main tables. The first is the expression matrix in the form of probe/gene intensities. The second table is the sample metadata.
# show class of the SummarizedExperiment class(genetic) #>  "RangedSummarizedExperiment" #> attr(,"package") #>  "SummarizedExperiment" # show the first table assay(genetic)[1:5, 1:5] #> GSM3453832 GSM3453833 GSM3453834 GSM3453835 GSM3453836 #> 0610010K14Rik 5.605891 5.914512 5.835002 5.761030 5.599307 #> 1110004F10Rik 5.362545 5.431240 5.339172 5.281284 5.454288 #> 1110032A03Rik 4.828588 4.852295 4.835784 4.749035 4.263849 #> 1110051M20Rik 3.872351 3.787890 4.268141 4.064035 4.400137 #> 1110059E24Rik 5.030677 4.814407 4.928870 4.911451 5.472552 # show the second table colData(genetic)[1:5,] #> DataFrame with 5 rows and 18 columns #> series_id sample_id pmid time media treatment #> <character> <character> <numeric> <numeric> <character> <character> #> GSM3453832 GSE122054 GSM3453832 31199203 48 MDI knockdown #> GSM3453833 GSE122054 GSM3453833 31199203 96 MDI knockdown #> GSM3453834 GSE122054 GSM3453834 31199203 0 none knockdown #> GSM3453835 GSE122054 GSM3453835 31199203 -48 MDI knockdown #> GSM3453836 GSE122054 GSM3453836 31199203 48 MDI none #> treatment_target treatment_type treatment_subtype treatment_time #> <character> <character> <character> <numeric> #> GSM3453832 slincRAD shRNA NA -1 #> GSM3453833 slincRAD shRNA NA -1 #> GSM3453834 slincRAD shRNA NA -1 #> GSM3453835 slincRAD shRNA NA -1 #> GSM3453836 none shRNA NA -1 #> treatment_duration treatment_dose treatment_dose_unit channels #> <numeric> <character> <character> <numeric> #> GSM3453832 NA NA NA 1 #> GSM3453833 NA NA NA 1 #> GSM3453834 NA NA NA 1 #> GSM3453835 NA NA NA 1 #> GSM3453836 NA NA NA 1 #> gpl geo_missing symbol_missing perturbation_type #> <character> <numeric> <numeric> <character> #> GSM3453832 GPL11202 0 0 genetic #> GSM3453833 GPL11202 0 0 genetic #> GSM3453834 GPL11202 0 0 genetic #> GSM3453835 GPL11202 0 0 genetic #> GSM3453836 GPL11202 0 0 genetic
The samples metadata were manually curated using controlled vocabularies to make comparing and combining the data easier. Table 1. show the columns and the descriptions of the metadata table.
|series_id||The GEO series identifier.|
|sample_id||The GEO sample identifier.|
|pmid||The pubmed identifier of the published study.|
|time||The time from the start of the differentiation protocol in hours.|
|media||The differentiation media MDI or none.|
|treatment||The treatment status: none, drug, knockdown or overexpression.|
|treatment_target||The target of the treatment: gene name or a biological|
|treatment_type||The type of the treatment.|
|treatment_subtype||The detailed subtype of the treatment.|
|treatment_time||The time of the treatment in relation to differentiation time|
|: -1, before; 0, at; and 1 after the start of the differentiation induction.|
|treatment_duration||The duration from the treatment to the collection of the|
|RNA from the sample.|
|treatment_dose||The dose of the treatment.|
|treatment_dose_unit||The dose unit of the treatment.|
|channels||The number of the channels on the array chip: 1 or 2.|
|gpl||The GEO GPL/annotation identifier.|
|geo_missing||The availability of the data on GEO: 0 or 1.|
|symbol_missing||The availability of the gene symbol of the probes in the GPL|
|perturbation_type||The type of the perturbation: genetic or pharmacological.|
The original articles where the datasets were first published are recorded by their pubmid ID. Please, cite the articles when using the related dataset.
To cite the package use: