Searching journal content for articles similar to Foulk et al. 25 (5): 725.

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  1. ...distribution to derive mean and standard deviation parameters (Fig. 3A, left). We then applied this parameterized model to the aggregated sequencing counts (Supplemental Fig. S6); discrepancies between the predicted and observed data revealed GC-content-related biases (Fig. 3A, right). We repeated this process...
  2. ...critical insights into transcription dynamics. Here, we combine transient transcriptome sequencing with transcription start site sequencing (TT-TSS-seq) to accurately map and quantify transcription initiation sites from nascent transcripts. Because transient metabolic labeling yields low-input RNA, we...
  3. ...understanding of G4 biology toward therapeutically targeting G4s in human diseases.G-quadruplexes (G4s) are four-stranded intramolecular structures that arise from the self-stacking of two or more guanine quartets (G-quartets), in which the four guanine molecules form a square planar arrangement in a cyclic...
  4. ...the many introns of a human gene are removed can substantially influence AS, while nascent RNA polyadenylation can affect RNA stability and decay. However, how splicing order and poly(A) tail length are regulated by genetic variation has never been explored. Here, we used direct RNA nanopore sequencing...
  5. ...motif and coding sequences. METTL2A knockdown alters expression of S100A4 mRNA isoforms, which contains METTL2A-mediated m3C sites. Notably, many transcripts with METTL2A-mediated m3C sites are upregulated upon METTL2A knockdown. We reveal the transcriptome-wide presence of m3C sites in poly(A) RNA...
  6. ...automatically adapts to sequencing error-rates and coverage levels per target region. TREAT integrates otter to enable end-to-end unified workflow for de novo motif characterization and downstream analysis, including TR visualization, outlier-based, and case-control comparisons (see Methods; Fig. 1A). Both...
  7. ..., and four origin recognition complex (ORC) components are all enriched in GSC-like cells compared with CySC-like cells (Table 1).View this table: In this window In a new window Table 1. Composition and function of select DNA replication and chromatin regulation complexesTo control for potential biases...
  8. ...-read technologies are unbiased and reveal a critical barrier to assembling sequences near repetitive regions. As large-scale sequencing projects move toward telomere-to-telomere assemblies in a wide range of organisms, recognizing and addressing these biases will be important to achieving truly complete...
  9. ...the estimated phased haplotypes of the target sample through iterative sampling. We briefly outline the computation involved in each sampling iteration below.In each iteration, a small but targeted conditioned reference panel is constructed, which is a subset of haplotypes from the original reference panel...
  10. ...into the effects of genetic variation on splicing and RNA abundance. Furthermore, the ability to directly sequence RNA enables the detection of RNA modifications in tandem with ascertaining the allelic origin of each molecule. Here, we leverage these advantages to determine allele-biased patterns of N6...
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