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ABSTRACT: Background
Birthweight reflects in utero exposures and later health evolution. Despite existing studies employing high-dimensional molecular measurements, the understanding of underlying mechanisms of birthweight remains limited.Methods
To investigate the systems biology of birthweight, we cross-sectionally integrated the methylome, the transcriptome, the metabolome and a set of inflammatory proteins measured in cord blood samples, collected from four birth-cohorts (n = 489). We focused on two sets of 68 metabolites and 903 CpGs previously related to birthweight and investigated the correlation structures existing between these two sets and all other omic features via bipartite Pearson correlations.Results
This dataset revealed that the set of metabolome and methylo
SUBMITTER: Alfano R
PROVIDER: S-EPMC7450273 | biostudies-literature | 2020 Sep
REPOSITORIES: biostudies-literature