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  1. ...). In a bacterial , the forms of DNA methylation are relatively limited (m6dA, m5C, m4C) and highly motif driven, which fundamentally ease the detection and differentiation of m6dA events from other DNA modifications. In contrast, m6dA events in eukaryotic s are much less abundant, weakly motif driven, and possibly...
  2. ...with DNase I (Methods), and sequenced cDNA products from WT, ddm1, and ddm1rdr6 using both Illumina short-read and Oxford Nanopore Technologies (ONT) long-read sequencing platforms (Supplemental Fig. S2). The two most productive elements, EVADE and the ATCOPIA52 subfamily element AT3TE76225, constituted 1...
  3. ....279292.124 ↵Liu X, Ni Y, Ye L, Guo Z, Tan L, Li J, Yang M, Chen S, Li R. 2024. Nanopore strand-specific mismatch enables de novo detection of bacterial DNA modifications. Genome Res (this issue) 34: 2025–2038. doi:10.1101/gr.279012.124 ↵Lohde M, Wagner GE, Dabernig-Heinz J, Viehweger A, Braun SD, Monecke...
  4. ...binding, crRNAs designed in a strand-directed manner help define sequencing directionality. For detecting duplications, Watson et al. designed plus-strand and minus-strand crRNA guides positioned within the duplicated sequence. Dephosphorylated DNA was split into two separate strand-specific cleavage...
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