Searching journal content for articles similar to Elso et al. 12 (9): 1428.

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  1. ...). To corroborate the observation, we investigated histone post-translational modifications (PTMs) by mass spectrometry (Johnson et al. 2004; Scheid et al. 2022), which confirmed an approximately eight- to 10-times-lower level of H3K9me2 but similar H3K9me1 levels in Spirodela relative to Arabidopsis (Supplemental...
  2. ...interactions of living organisms, and developing precise techniques to detect genomic differences between species. Nevertheless, the increase in biological data also necessitates algorithmic advances to capture the most useful information.As species evolve and diverge, they acquire new traits. This leads...
  3. ...with neither occupied CTCF motifs nor ChromHMM state annotations linked with enhancer/promoter activity.Epigenomic pileup analysisAs hundreds or thousands of stripes may be called, we sought to analyze our findings at a mass scale, so the aggregate epigenomic pileup analysis visualizes context sequence...
  4. ...for the detection of many novel variants, especially in the previously unresolved regions. They also found that their novel reference reduces the number of false-positive calls mainly in protein-coding genes, and they highlight the increased sensitivity for detection of rare variants and singletons (Aganezov et al...
  5. ...capacity. The animals can replace any part of their body when dissected into multiple fragments. Each part usually regrows into a new organism within 2–3 days (Fujisawa 2003; Tomczyk et al. 2015), as demonstrated in the most extreme case from a fragment of only 1% of the body mass (Shimizu et al. 1993...
  6. ...framework for multiple ST analysis tasks, including spatial domain detection and cell cycle identification. Although these methods have successfully analyzed individual slices, they remain limited to two-dimensional (2D) analyses owing to their single-slice focus.As the availability of SO data derived from...
  7. ...with the form count ∼ cohort using the MASS package in R (Venables and Ripley 2002). dnSNV counts were modeled as a negative binomial random variable with a log link function, rather than a Poisson random variable, as preliminary exploration of the count data revealed mild overdispersion (mean = 19.4, variance...
  8. ...the sequence of the underlying repeat unit. Although several methods exist, they often exhibit low accuracy when the repeat unit length increases or the number of copies is low. Furthermore, methods capable of handling highly mutated sequences remain scarce, highlighting a significant opportunity...
  9. ...; Pleguezuelos-Manzano et al. 2020). This enrichment is attributed to the particularly narrow minor groove of these sequences, which promotes colibactin binding (Dziubańska-Kusibab et al. 2020). Recent work has found that a colibactin-associated mutational signature is detected in 5%–10% of colorectal cancers...
  10. ...the corresponding N-terminal peptide generated by tryptic digest is too large (38 amino acids) for mass spectrometric detection. Also, the majority of N-terminal peptides mapped within a single nucleotide of the TISs predicted by ribosome profiling data.View larger version: In this window In a new window Figure 4...
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