Searching journal content for articles similar to Lee et al. 14 (6): 1085.

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  1. ..., we performed weighted gene coexpression network analysis (WGCNA) across four tissues (Supplemental Fig. S8A). The analysis revealed that LOC101800576 and LOC101790890 were assigned to the shell gland ME3 module, GLP2R to the spleen ME7 module, and LOC119713219 to the ovary ME6 module (Supplemental...
  2. ...and so fail to fully capture population heterogeneity. Bayesian optimized networks obtained by assimilating omic data (BONOBO) is a scalable Bayesian model for deriving individual sample-specific coexpression matrices that recognizes variations in molecular interactions across individuals. For each...
  3. .../4 and spinal MNs). The initial analysis showed that only 17 DEGs were shared across all data sets (Supplemental Fig. S6A,B). RNA-seq data sets revealed a substantially larger number of DEGs between CN3/4 and spinal MNs compared with microarray analyses (Supplemental Fig. S6A), and we thus focused on the RNA...
  4. ...and mouse TR–target interactions.Here we outline a framework to identify and rank experimentally derived TR–target relationships by aggregating ChIP-seq and perturbation data sets from both mouse and human. We describe the degree of similarity across experiments and note characteristics of each data type...
  5. ...observed are likely dominated by differential expression across cell types, not coexpression within cell types (Aibar et al. 2017).Our study does have some limitations. First, our analysis of cell-type-level coexpression is based on a single (albeit large and unusually deeply sequenced) data set that used...
  6. ...-based stratification of SLE patients is relatively stable across their longitudinal samples and the relationship between changes in gene transcriptome-derived status and changes in the plasma levels of specific pro-inflammatory cytokines or chemokines is not one-to-one.Weighted gene coexpression network analysis...
  7. ...Table S1A).We calculated coexpression fold enrichment scores for the eight NDD gene sets and four control gene sets across the six major cell types (Fig. 1A; Supplemental Fig. S2). In general, NDD gene sets showed significantly higher coexpression than control gene sets (Fig. 1A; Supplemental Figs. S2...
  8. ...against viruses. Despite its importance, transcriptomic dynamics with fine temporal resolution across the entire digestion cycle have not yet been reported. To fill this gap, we conducted a transcriptomic analysis of A. aegypti female midguts across a 72-h bloodmeal digestion cycle for 11 time points...
  9. ...transcripts derived from sRNA-seq data sets are comparable to those from total RNA-seq experiments (R2 ranging from 0.33 to 0.76). Analyses across multiple tissues and species show similar correlations, indicating that the approach is applicable across organisms. We confirm that transcript half...
  10. ...uniquely mapped reads were aligned across all data sets, with summed coverage for each tissue-enriched or cell type–enriched transcriptome ranging from over 100 million to over 300 million reads (Supplemental Fig. S1).View larger version: In this window In a new window Figure 1. TRAP-seq identifies tissue...
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