Searching journal content for articles similar to Emberton et al. 15 (10): 1441.

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  1. ...inputs: the raw library, the assembly, and the BUSCO gene set. As such, this tool can be easily integrated into any automatic pipeline to annotate TEs.DiscussionWe have shown that MCHelper increases TE libraries accuracy and completeness, producing longer and unfragmented TE annotations across eukaryotic...
  2. ...functional molecules. The biological function of a given protein is dictated by the arrangement of the atoms and functional groups in its three-dimensional (3D) structure. Therefore, variation in protein 3D structure is an essential source of information to explain how coding sequence variants impact gene...
  3. ...-base resolution methylation levels for individual CpG sites across the . These resources also annotate hypomethylated regions commonly linked to gene promoters, as well as allele-specific methylation patterns relevant to genomic imprinting. Notable examples include MethBase (Song et al. 2013), MethBank (Zhang et...
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  4. ...ultra-large genomic reference sets (e.g., Parks et al. 2018; McDonald et al. 2024), often used with marker genes (Asnicar et al. 2020; Balaban et al. 2024). Using these data sets with k-mers-based methods, however, runs into a mundane but key limitation—the memory needed to use these s as reference...
  5. ...for the cerebellum (Fig. 1B), heart (Fig. 1C), and kidney (Fig. 1D). The correlation between gene expression levels from the RNA-seq and sRNA-seq libraries was highest in brain (R2 = 0.76) and cerebellum (R2 = 0.62).View larger version: In this window In a new window Figure 1. Comparison of the expression levels...
  6. ...al. 2015) and reformatted to follow the naming conventions of panEDTA. The curated Arabidopsis library was provided to panEDTA with the “‐‐curatedlib” parameter.This study utilized previously generated assemblies of the 26 maize NAM founder lines (Hufford et al. 2021), and their assemblies and gene...
  7. ...at different times during the 4sU labeling period. Moreover, peak identification can be computationally challenging for genes with low read coverage or uneven nascent transcription profiles, limiting the number of analyzable genes. Additionally, the 10- to 40-min time windows used in DRB/TTchem-seq restrict...
  8. ..., this is not because of differences in expression levels, as the gene on which the edit is located (Htra1) is expressed in all involved clusters.Overall, this constitutes evidence that RNA-editing events may be seen in Chromium scRNA-seq libraries and used to infer heterogeneous presentation of RNA editing. Although...
  9. ...profiles of P. pacificus nematodes in response to diverse microbiota and used them to test the hypothesis that the adaptation to novel microbiota might be facilitated by the evolution of novel genes (Athanasouli et al. 2023). This revealed evidence that novel genes might be preferentially integrated...
  10. .... Recently, systematic evaluation of the impact of CREs on gene expression has become possible with CRISPR perturbations (Fulco et al. 2019), but only a small subset of CREs can be evaluated in the . Meanwhile, the evaluation is restricted to a small number of cell types. Due to its high cost...
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