Additional file 2: of Divergent neuronal DNA methylation patterns across human cortical development reveal critical periods and a unique role of CpH methylation
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https://springernature.figshare.com/articles/dataset/Additional_file_2_of_Divergent_neuronal_DNA_methylation_patterns_across_human_cortical_development_reveal_critical_periods_and_a_unique_role_of_CpH_methylation/9905807/1
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Table S1. WGBS Phenotype, Sequencing Data. Table S2. RNA Phenotype, Sequencing Data. Table S3. Number of cytosines measured and distribution of methylation by context. Table S4. Number of Low Methylation Regions (LMRs) and Unmethylated Regions (UMRs) per sample. Table S5. Cell type-specific, developmental differentially methylated regions (cdDMRs). Table S6. mC association with cell type and age in postnatal cell type-specific samples. Table S7. Molecular function gene ontology enrichment for genes including exons whose expression is associated with cytosine methylation levels. Table S8. GWAS traits assessed using LDSC. Table S9. Stratified linkage disequilibrium score regression results. Table S10. Enrichment of DMRs and mCpH for disease-associated gene sets. Table S11. Enrichment for disease gene sets in DNAm-splicing association features. Table S12. Variable dictionary for Table 1. (XLSX 437 kb)
提供机构:
Hyde, Thomas; Xia, Wei; Tao, Ran; Jaffe, Andrew; Kleinman, Joel; Shin, Joo Heon; Ivanov, Nikolay; Weinberger, Daniel; Jia, Yankai; Collado-Torres, Leonardo; Burke, Emily; Price, Amanda; Ma, Liang
创建时间:
2019-09-26



