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pmid:26217797

Prenatal alcohol exposure alters gene expression in the rat brain: Experimental design and bioinformatic analysis of microarray data.

Alexandre A Lussier · Katarzyna A Stepien · Joanne Weinberg · Michael S Kobor

Data in brief · 2015 doi:10.1016/j.dib.2015.05.007

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Prenatal alcohol exposure alters gene expression in the rat brain: Experimental design and bioinformatic analysis of microarray data.
doi
10.1016/j.dib.2015.05.007
pmid
26217797
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Alexandre A Lussier
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Katarzyna A Stepien
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Joanne Weinberg
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Michael S Kobor
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Data in brief
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2015
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We previously identified gene expression changes in the prefrontal cortex and hippocampus of rats prenatally exposed to alcohol under both steady-state and challenge conditions (Lussier et al., 2015, Alcohol.: Clin. Exp. Res., 39, 251-261). In this study, adult female rats from three prenatal treatment groups (ad libitum-fed control, pair-fed, and ethanol-fed) were injected with physiological saline solution or complete Freund׳s adjuvant (CFA) to induce arthritis (adjuvant-induced arthritis, AA). The prefrontal cortex and hippocampus were collected 16 days (peak of arthritis) or 39 days (during recovery) following injection, and whole genome gene expression was assayed using Illumina׳s RatRef-12 expression microarray. Here, we provide additional metadata, detailed explanations of data pre-processing steps and quality control, as well as a basic framework for the bioinformatic analyses performed. The datasets from this study are publicly available on the GEO repository (accession number GSE63561).
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In order to correct for these unknown variables, as well as significant batch effects in the two datasets, surrogate variable analysis (sva) was used to generate variables representative of expression heterogeneity within the two datasets [7].
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sections[14] "Differential expression analysis" paragraph 2
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In order to correct for these unknown variables, as well as significant batch effects in the two datasets, surrogate variable analysis (sva) was used to generate variables representative of expression heterogeneity within the two datasets [7].
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Probe-level data for this study were deposited on the GEO (GSE63561), along with metadata describing experimental treatment groups. As described, spatial artifacts were masked from the dataset and data were log 2-transformed prior to submission of raw and quantile-normalized data. Moreover, due to GEO submission requirements, the datasets were filtered to include only probes associated with a gene. As such, the current GEO files do not contain any control probes, although these additional data are available upon request.
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Probe-level data for this study were deposited on the GEO (GSE63561), along with metadata describing experimental treatment groups. As described, spatial artifacts were masked from the dataset and data were log 2-transformed prior to submission of raw and quantile-normalized data. Moreover, due to GEO submission requirements, the datasets were filtered to include only probes associated with a gene. As such, the current GEO files do not contain any control probes, although these additional data are available upon request.
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This method identifies eigenvectors of variation not associated with primary variables, which can then be incorporated as covariates during linear modeling to remove unwanted sources of heterogeneity.
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Surrogate variables generated by sva were included as covariates in linear modeling of gene expression using the limma package in the statistical program R [11].
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As the effects of experimental treatments were subtle, the false-discovery rate (FDR) was controlled at 25% (q-value <0.25).
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Prenatal alcohol exposure alters steady-state and activated gene expression in the adult rat brain
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Distribution of sample numbers between different prenatal treatments, termination days, and adjuvant-induced arthritis (AA) treatments for the prefrontal cortex (PFC) and hippocampus (HPC).
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atal alcohol exposure alters gene expression in the rat brain: Experimental design and bioinformatic
[1]
cohol exposure alters gene expression in the rat brain: Experimental design and bioinformatic
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in the prefrontal cortex and hippocampus of rats prenatally exposed to alcohol under both ste
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., 39, 251-261). In this study, adult female rats from three prenatal treatment groups (ad lib
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imental design and bioinformatic analysis of microarray data.
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ssayed using Illumina׳s RatRef-12 expression microarray. Here, we provide additional metadata, detai
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mental design prior to sample collection and microarray analysis. Adult female rats from one of thre
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Complete file
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