Searching journal content for articles similar to McCaffrey et al. 27 (11): 1904.

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  1. ...the at regions dense in CCGG sites. RRBS captures ∼60% of gene promoters, thus producing crucial regulatory information while requiring very little input sample (Gu et al. 2011). The low input implies that fewer reads are necessary for accurate sequencing, allowing for high-throughput, low-cost methylation...
  2. ...for rooting for 3 months and finally planted in soil for characterization.DNA extraction and high-throughput sequencingA total of 3 original plants (CK), 27 regenerated plants under different conditions (LS, LL, HS, HL, CA), and 12 “Beni hoppe” plants were used. For each sample, the young leaves were...
  3. ...Research High-throughput chromatin motion tracking in living yeast reveals the flexibility of the fiber throughout the Houssam Hajjoul,1,2,6 Julien Mathon,1,2,6 Hubert Ranchon,1,2 Isabelle Goiffon,2,3 Julien Mozziconacci,4,5 Benjamin Albert,2,3 Pascal Carrivain,4,5 Jean-Marc Victor,4,5 Olivier...
  4. ...the accuracy of calling and assembly (Supplemental Figs. S20–S23). Additionally, we examined whether contig sequences were present within cell populations before transfection with DN-TERT and telomere crisis. Using a single-molecule assay to detect a contig present in LIG3−/−:NC3: sample 53 (DB53_1501), we...
  5. ...rearrangements of the kind frequently observed in human cancers. We have characterized more than 1400 telomere fusion events at the single-molecule level, using a combination of high-throughput sequence analysis together with experimentally induced telomeric double-stranded DNA breaks. We show that a single...
  6. ..., and the released DNA can be sequenced to identify all DNA sequences bound to the protein of interest using high-throughput platforms (Park 2009). Standard controls include comparing this immunoprecipitation to DNA binding by nonimmunized IgG raised in the same species as the protein targeting antibody, using q...
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  7. ...-read sequencing allows for high-throughput characterization of the locus, and efforts are underway to gather germline diversity across human populations (Rodriguez et al. 2020). However, although this strategy yields highly accurate reads, it does not contiguously resolve the entirety of the locus and may miss...
  8. ...for FSHD1 fibroblasts from Cas9-targeted sequencing. Single-molecule and smoothed methylation plots for 4q and 10q D4Z4 alleles from the FSHD1 samples (A) 19,187, (B) 17,706, and (C) 12,566, generated using NanoMethViz (Su et al. 2021, 2025). The locations of DUX4 exons are shaded in gray on the smoothed...
  9. ...and disease diagnostics. DNA methylation signals directly obtained from long reads enhance the utility of single-molecule long-read sequencing technologies by enabling molecular phenotypes to be interpreted, and by allowing the identification of the parent of origin of de novo mutations. Despite this recent...
  10. ..., Spain; 10Gene Expression and mRNA Metabolism Laboratory, CIPF, 46012 Valencia, Spain ↵11 Joint first authorship. Corresponding author: aconesa@ufl.edu, aconesa@cipf.esAbstractHigh-throughput sequencing of full-length transcripts using long reads has paved the way for the discovery of thousands of novel...
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