Searching journal content for articles similar to Reid et al. 21 (3): 477.

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  1. ...differentiate both ABC and GCB with the same edge sign from unclassified DLBCL, is a peptide proteotypic for DNA methyltransferase 1 (DNMT1). DNMT1, which belongs to a family of DNA methyltransferases that catalyze the transfer of the methyl moiety from S-adenosylmethionine to DNA, plays an important role...
  2. ...; Eusebi et al. 2020). Many studies compare and utilize different types of marker techniques, including mitochondrial DNA barcoding (mtDNA) (Guo et al. 2006), the Y-Chromosome technique (Bruford et al. 2003), minisatellite and microsatellite markers (Ćurković et al. 2016), and single...
  3. ...(Supplemental Fig. S2). We tested the sgRNA of the two lines through simple genomic PCR and found that both phenotypes were theoretically related to their predicted functions (Paine et al. 2019; Schimmel et al. 2021). The target regions of Peanuts (KWMTBOMO05973) and DNA primase large subunit (KWMTBOMO01805...
  4. ...) identifies and subsequently repairs damaged DNA (Ciccia 40 and Elledge 2010; Molinaro et al. 2021). Primary DNA repair pathways include nucleotide 41 excision repair (NER), base excision repair (BER), mismatch repair (MMR), homologous 42 recombination (HR), non-homologous end joining (NHEJ), and interstrand...
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  5. ...between scRNA-seq and scATAC-seq pose challenges for identifying different cell types, which hinders the discovery of novel types. In this study, we propose a new label transfer tool scSHEFT, which simultaneously considers gene expression count data, peak count data, and Gene Activity Scores as inputs...
  6. ...damage (Vollmer et al. 1997), and a CFP under control of a constitutive promoter into a low-copy plasmid (Fig. 4A). The CFP tag allowed us to identify reporter cell colonies and normalize DNA damage–induced fluorescence (YFP) to cell numbers in reporter colonies.View larger version: In this window...
  7. .... This could be achieved by using enzymes that enable target enrichment by depleting unwanted sequences from HTS libraries. For example, the duplex-specific nuclease (DSN) selectively digests double-stranded DNA molecules, and can be used to eliminate highly abundant sequences in a controlled denaturation...
  8. ..., and the complete training protocol, enabling exact replication of the model architectures and experimental results.Feature encoding schemesMore than 24 common feature encoding schemes are widely used in epigenetic site prediction. In the work of EpiTEAmDNA, Li et al. (2023) demonstrated that 10 feature encoding...
  9. ...than one carbapenem-resistant bacterial species. All isolates underwent Illumina sequencing as previously described (Gomez-Simmonds et al. 2018b). Briefly, genomic DNA was extracted from bacterial broth cultures using the QIAamp DNA Blood Mini Kit or QIAamp 96 QIAcube HT DNA isolation Kit (Qiagen...
  10. .... An in vitro CRISPR/Cas9 RNA-directed nickase system directs the specific labeling of human (TTAGGG)n DNA tracts in s that have also been barcoded using a separate nickase enzyme that recognizes a 7bp motif -wide. High-throughput imaging and analysis of large DNA single molecules from s labeled in this fashion...
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