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  1. ...were prepared with a starting amount of 300 ng and amplified in 14 PCR cycles. Libraries were profiled in a High Sensitivity DNA on a 2100 Bioanalyzer (Agilent Technologies) and quantified using the Qubit dsDNA HS Assay kit, in a Qubit 2.0 Fluorometer (Life Technologies). All libraries from the two...
  2. ...are incubated with BrdU, followed by nuclei isolation. GFP-positive nuclei are then sorted by DNA content, separating into one of four S-phase fractions: early, early-mid, late-mid, or late replicating. Next, the BrdU-containing DNA is immunoprecipitated and prepared for sequencing to identify genomic locations...
  3. ...called “fountains,” which have also been reported in zebrafish and mice. These are population average reflections of DNA loops originating from distinct genomic regions and are ∼20–40 kb in C. elegans. Hi-C analysis upon cohesin and WAPL-1 depletion supports the idea that cohesin is preferentially loaded...
  4. ...complementary to the first adapter, and the other DNA end was ligated to the second adapter (Fig. 1D, blue). Following PCR amplification using primers complementary to both adapters, the resulting libraries were submitted for high-throughput sequencing. The resulting sequencing reads were mapped to the yeast...
  5. ...before (DAP-seq) and after PCR amplification (ampDAP-seq), where the amplification depletes the library of DNA methylation. MBD5 and MBD6 showed sequence enrichment, but only for DAP-seq, where DNA methylation was present, and with binding site profiles that closely match those identified by Ch...
  6. ...sequencing (scRNA-seq) and single-cell DNA methylation (scDNAm) data face limitations, including unidirectionality, inadequate modeling of context-specific DNA methylation–expression associations, neglect of biological relevance in evaluation, and poor performance in limited paired training data. To fill...
  7. ...-stranded DNA (dsDNA) with a single-cycle polymerase chain reaction (PCR) reaction consisting of 10 µL of washed Dynabead-bound sample, 12 µL of 2X Q5 high-fidelity DNA polymerase (NEB), and 2 µL of P5_primer_short (Supplemental Table S4). Samples are incubated for 2 min at 98°C followed by 5 min at 65°C...
  8. ...@cuhk.edu.hkAbstractThe discovery of circulating fetal and tumor cell-free DNA (cfDNA) molecules in plasma has opened up tremendous opportunities in noninvasive diagnostics such as the detection of fetal chromosomal aneuploidies and cancers and in posttransplantation monitoring. The advent of high-throughput sequencing...
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  9. ...contributions from sequencing data of plasma cfDNA (Fig. 1). The individuals studied were participants who had undergone screening for NPC (Chan et al. 2017, 2023). These subjects underwent plasma EBV DNA testing by real-time polymerase chain reaction (PCR) for NPC screening. The screening trial was conducted...
  10. ...rather than by subsequent insertion or rearrangement after insertion. In addition, insertion of NORGs can be accompanied by filling with nonorganelle DNA, resembling the insertion pattern of mtDNA in human somatic cells (Ju et al. 2015). Similarly, particle bombardment in transgenic papaya SunUp resulted...
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