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Data Card: DILGOM Whole-Blood Microarray Dataset (E-TABM-1036)
Summary
Expression + sample metadata + feature metadata for E-TABM-1036, which profile whole-blood gene expression in a population-based cohort from the Helsinki/Vantaa area of Finland. Profiled on Illumina HumanHT-12 v3 Expression BeadChip. This accession has no obesity or metabolic-syndrome phenotype data. These are the 'healthy' controls.
Source accession
| Accession | N (SDRF rows) | Platform | Submitter |
|---|---|---|---|
| E-TABM-1036 | 518 | Illumina HumanHT-12 v3 | Inouye (Wellcome Trust Sanger Institute) |
Files
sample_metadata.parquet— one row per sample:sample_id,accession,age_band,sex. This is the full extent of usable per-sample metadata in the SDRF — see Notes.feature_metadata.parquet— one row per probe (IlluminaID): annotation fromilluminaHumanv3.db(SYMBOL,ENTREZID,ENSEMBL,GENENAME,UNIPROT) plus reannotation QC fields from the package's internalExtraInfotable (ProbeQuality,CodingZone,GenomicLocation,SecondMatches,OtherGenomicMatches,RepeatMask,OverlappingSNP,ProbeSequence)expression/— partitioned parquet dataset (byaccession, for schema consistency with other datasets in this collection even though there is only one accession here), long format:IlluminaID,sample_id,accession,value
Expression value processing (from the accession's IDF)
Per the submitter's own protocol description (bioassay_data_transformation
protocol, P-TABM-5309):
"Normalized intensities were calculated via quantile normalization of the weighted-sums of the raw replicate intensities. Weighting was by number of beads contributing to raw signal. Final intensities were arrived at by a log2 transformation after quantile normalization."
RNA source: PAXgene Blood RNA Tubes, whole blood (per protocol P-TABM-5305), amplified via in vitro transcription (P-TABM-5306) and hybridized to HumanHT-12 v3 BeadChips (P-TABM-5307).
Provenance / reproducibility
Data retrieved with ArrayExpress::getAE() against BioStudies (EBI), with
probe annotation from Bioconductor's illuminaHumanv3.db. See
pull_dilgom.R
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