Searching journal content for articles similar to Rice et al. 14 (1): 116.

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  1. ...contributed equally to this work. Corresponding authors: mi.jain@northeastern.edu,kimberley.billingsley@nih.gov, cornelis.blauwendraat@nih.govAbstractDNA methylation most commonly occurs as 5-methylcytosine (5mC) in the human and has been associated with human diseases. Recent developments in single...
  2. ...an accessible user interface. Ultimately, our study provides novel 31 insights into the DNA damage response kinetics in Tetrahymena. 32 33 Introduction 34 Environmental genotoxic stressors induce DNA damage, posing a threat to stability 35 and integrity. Therefore, maintaining a carefully regulated orchestra...
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  4. ...DNA samples. Leveraging somatic SNVs and fusions, LongSom found subclones with different predicted treatment outcomes. In summary, LongSom enables de novo variant detection without the need for normal samples, facilitating the study of cancer evolution, clonal heterogeneity, and treatment resistance...
  5. ...method addresses key challenges in detecting both short and long tandem repeats from highly erroneous sequences, areas in which existing tools often fall short. EquiRep was applied to two applications: reconstructing the repeat unit from satellite DNAs and reconstructing the circular RNAs from rolling...
  6. ...that elevated replication gene expression in GSC-like cells reflects a true biological difference rather than differences in cell-cycle-phase distribution.We next tested whether the enrichment of DNA replication factors detected in GSC-like cells from the upd tumor also occurs in GSCs from nontumor wild...
  7. ...was used as the initial material for the RNA sample preparation. Briefly, mRNA was purified from total RNA using poly(T) oligo-attached magnetic beads. Then, the RNA was fragmented into short strands in NEBNext first-strand synthesis reaction buffer under an elevated temperature. Subsequently, the first cDNA...
  8. ...@cmh.edu , guil.bourque@mcgill.ca Abstract Structural variants (SVs) are omnipresent in human DNA, yet their genotype and methylation statuses are rarely characterized due to previous limitations in assembly and detection of modified nucleotides. Also, the extent to which SVs act as methylation quantitative trait...
  9. ..., and reduction in the cost of DNA sequencing, it has become possible to rapidly identify most variants in the of a single individual (Gorzynski et al. 2022; http://www..gov/sequencingcostsdata). Most clinical geneticists follow the American College Medical Genetics/Association for Molecular Pathology (ACMG...
  10. ...oligonucleotides deposited in the borders of the double-barcoded deposited probes (TRITC channel) (Fig. 2A), the aforementioned procedure was applied, leading to a sequencing library presenting DNA fragments ranging between 300 and 1000 bp (Fig. 2D). More than 250 million reads were Illumina...
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