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ABSTRACT: Background
Differential gene expression analysis is important to understand pregnancy processes and disease development. However, no non-invasive and comprehensive methods exist to identify differentially expressed genes (DEGs) in the fetus and placenta during pregnancy or pregnancy complications. Nucleosome footprints in maternal peripheral blood plasma cell-free DNA (cfDNA) reflect the gene expression profile of the cell of origin, mainly immune cells in the maternal blood and placenta. This study aimed to validate the feasibility of detecting changes in gene expression profiles as differentially depth gene (DDGs) based on plasma nucleosome footprints as a potential biomarker for pregnancy and pre-eclampsia.Methods
Deep sequencing was performed on separated plasma cfDNA c
SUBMITTER: Li K
PROVIDER: S-EPMC11916520 | biostudies-literature | 2025 Mar
REPOSITORIES: biostudies-literature