| Autor: |
Wang, Xuting, Cho, Hye-Youn, Campbell, Michelle R., Panduri, Vijayalakshmi, Coviello, Silvina, Caballero, Mauricio T., Sambandan, Deepa, Kleeberger, Steven R., Polack, Fernando P., Ofman, Gaston, Bell, Douglas A. |
| Rok vydání: |
2022 |
| Předmět: |
|
| DOI: |
10.6084/m9.figshare.19682108 |
| Popis: |
Additional file 1. Table S1. Cohort demographics by bronchopulmonary dysplasia (BPD) status (n = 107). Table S2. Distribution of cord blood cell types and methylation status of a tobacco smoke epigenetic biomarker in neonates with or without bronchopulmonary dysplasia (BPD). Table S3. Differentially methylated CpG sites associated with nucleated red blood cell (NRBC) counts. Table S4. Differentially methylated CpG sites associated with bronchopulmonary dysplasia (BPD) risk and their annotated gene information. Table S5. The number of probes identified by differential methylation analysis. Table S6. Association of stochastic epimutation load (EML) with bronchopulmonary dysplasia (BPD) and other covariates. Table S7A. Biological functions and pathways of the genes annotated to the differentially methylated CpG sites (FDR 5%) associated with bronchopulmonary dysplasia (BPD) risk. Table S7B. GOmeth enriched GO terms on CpGs associated with BPD risk. Table S7C. GOmeth enriched KEGG pathways on CpGs associated with BPD risk. Table S8. cDNA microarray determined differentially expressed genes in cord blood cells of infants with bronchopulmonary dysplasia (BPD). Table S9. DNA CpG methylation sites associated with gestational age (GA) or birth weight (BW). |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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