Searching journal content for articles similar to Yang et al. 31 (3): 349.

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  1. ...) were performed. Finally, data analysis and visualization were performed to generate CNV, RT, and gene expression profiles (9).PARTAGE sample preparation preserves DNA and RNA integrityTo test PARTAGE, we exploited the HepG2 human cell line, a reference cell line used at the ENCODE (The ENCODE Project...
  2. ...–specific cis-regulatory DNA elements (CREs), we pinpoint 141 ADNC-associated genes. Using gene set enrichment analysis (GSEA) and network proximity analysis, we further identify nine candidate repurposable drugs that were associated with these ADNC-related genes. In summary, this cell type–specific multiomic...
  3. ...analysis by incorporating the regulatory annotation of open chromatin regions, as assessed through ATAC-seq, across 63 tissues available in the Encyclopedia of DNA Elements (ENCODE) (The ENCODE Project Consortium et al. 2020). The ENCODE data exhibited wide variation in sample sizes across tissues, leading...
  4. ...). Statistical modeling showed no significant compositional changes with age after correcting for multiple tests.View larger version: In this window In a new window Figure 2. Profiling of age-associated gene expression variations across substantia nigra cell subclasses. (A) UMAP representation of all nuclei...
  5. ...transcriptomic and epigenomic data across 26 human tissues from the EN-TEx (ENCODE-GTEx) project. We uniformly annotate promoters with chromatin features (histone modifications, chromatin accessibility, and DNA methylation), sequence motifs, and evolutionary conservation, generating an online catalog. Leveraging...
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  6. ...feature analysis modules to explore RTE dynamics in a user-defined condition. To our knowledge, scARE represents the first systematic investigation of RTE dynamics at the single-cell level within the context of neurodegenerative diseases.Transposable elements (TEs) are DNA elements that are capable...
  7. ...-co1 (C) and Mt-cyb (E).DiscussionWe report a class of previously undocumented chimeric mtRNAs, which increase in multiple conditions associated with mitochondrial pathology and predict mtDNA deletion frequency and altered transcription of genes essential for mitochondrial function. The new class...
  8. ...independent of copy number changes; these processes increase the tumor mutation burden and thus the likelihood of novel driver mutations. Mutations arise through impairments in DNA-damage repair pathways (Wu et al. 2020), endogenous processes including APOBEC mutagenesis, and exogenous factors such as smoking...
  9. .... Order determined by a coin flip. Corresponding author: braphael@princeton.eduAbstractSpatially resolved transcriptomics (SRT) technologies measure gene expression across thousands of spatial locations within a tissue slice. Multiple SRT technologies are currently available and others are in active...
  10. ...semantic entailment, generating multiple approximate models of 89 GO, and aggregating predictions across these models to exploit GO’s axiomatic 90 structure. Recent state-of-the-art methods have increasingly incorporated InterPro 91 domains (Paysan-Lafosse et al. 2023) as explicit features. These domains...
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