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  1. ...a transposase domain derived from an Hsmar1 insertion conserved in primates, providing functional DNA-binding to target methylation (Cordaux et al. 2006). Such exaptation and domestication events can often be identified by the occurrence of chimeric transcripts, which are mRNAs with both gene- and TE...
  2. ...) Models are compared based on their ability to predict experimental ATAC-seq at 4-bp resolution from an input of 2048-bp long DNA sequences. (B) Models based on existing methods include CNN, LSTM, and dCNN-based architectures. Each model has a convolution-based stem to extract genomic features. (C) Models...
  3. ...; SPRI beads are mostly used for polymerase chain reaction (PCR) cleanup where the fragment length is much shorter (Rodrigue et al. 2010; Stortchevoi et al. 2020). In addition, the library is a complex of motor protein and DNA, and so alcohol-based precipitation and washes are not compatible. In our...
  4. ...-LSK110 kit LSK109 (Oxford Nanopore Technologies), sequenced on a full R10.4.1 flow cell, and basecalled with Dorado version 0.5.3 (https://github.com/nanoporetech/dorado).Short-read Illumina DNA and RNA libraries were prepared using the KAPA HyperPlus PCR-free and KAPA mRNA capture kits (Roche...
  5. ...sets of 11 species using 14 feature encodings respectively, taking CNN as an example (Supplemental Fig. S6).As shown in Figure 4A, the 4mC data sets from EpiTEAmDNA were categorized into plant, animal, and microbial groups. Cross-prediction results showed that the diagonal species achieved the highest...
  6. ...DNAm sequencing technologies, the scDNAm data often suffer from low coverage, high sparsity, and substantial technical noise (Kremer et al. 2024). These limitations arise from factors such as limited DNA input, bisulfite conversion inefficiencies, and sequencing dropouts, which together compromise the reliability...
  7. ...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...
  8. ...analog bromodeoxyuridine (BrdU) to label replicating DNA. Next, GSC-like or CySC-like nuclei were extracted and sorted via flow cytometry into four S-phase fractions corresponding to early, early-mid, late-mid, and late S phase, based on their DNA content (Fig. 4A; Supplemental Fig. S5A–C). Brd...
  9. ...that are densely DNA methylated and invaded by centrophilic retrotransposons. In some cases, the retrotransposons become the sites of CENH3 loading. We review the structure of plant centromeres, including monocentric, holocentric, and metapolycentric architectures, which vary in the number and distribution...
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  10. ...(G) primer presenting a known adapter sequence at its 5′-extremity (Adpt1), followed by Klenow polymerase extension (Fig. 1E). Finally, DNA arrays are exposed again to alkaline conditions for releasing the elongated complementary DNA sequence and are collected in a tube for performing two rounds of PCR...
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