Searching journal content for articles similar to Siefert et al. 27 (8): 1406.

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  1. ...-translational modifications, play a crucial role in regulating programs integral to a cell's identity, like gene expression and DNA replication. However, the transcriptional, chromatin, and replication timing profiles of adult stem cells in vivo remain poorly understood. Containing germline stem cells (GSCs) and somatic cyst...
  2. ....e., computational representations of transcripts depicting their transcription start and termination sites (TSS and TTS) and intron composition (Amarasinghe et al. 2020; Marx 2023). Most lrRNA-seq experiments rely on cDNA libraries, as they provide high sequencing throughput and accuracy. However, reverse...
  3. ...to the transcription machinery. As a result, transcription levels can undergo repression leading to a silencing effect of the associated gene. The dominant form of DNA methylation in terminally differentiated human cells occurs proximal to a guanosine residue, and the resulting loci are often referred to as CpG sites...
  4. ...that H4K16 modification is dispensable for replication and gene expression.Animal cells duplicate large, complex s by initiating replication at distinct locations within the at different times during S phase. An evolutionarily conserved feature of this regulatory paradigm is a temporal order of DNA...
  5. ...states, except state 1 (TSS), state 8 (AT-rich heterochromatin), and state 4 (intergenic, Polycomb, and AT-rich), which are most variable.Interplay between DNA replication origins and transcriptional programsThe relationship between ORI activity and transcriptional programs during development has been...
  6. ...transcriptionally distinct subpopulations and genetic subclones. At the same time, simultaneous unbiased assessment of DNA and RNA from an individual cell remains challenging (Dey et al. 2015; Macaulay et al. 2015; Wang et al. 2017).Computational approaches for bulk sequencing data detect copy number variations...
  7. ...profile of the whole human genome by massively parallel sequencing of nascent BrdU-labeled replicating DNA. These data were compared to the neutral substitution rates along the human genome, obtained by aligning human and chimpanzee genomes using macaque and orangutan as outgroups. All substitution rates...
  8. ...interaction with an 18-bp indel in the TAL1 superenhancer. Additionally, we identified TFs that bind to three uncharacterized DNA motifs identified in DNase footprinting assays. We anticipate that these enhanced yeast one-hybrid approaches will expand our capabilities to study genetic variation...
  9. ...and binding motif. (B) Immunoprecipitation of DNA sequence associated with large multiprotein complex results in artifactual indirect enrichments for a wide range of transcription factors. (C ) Active enhancers exhibit a range of ChIP-seq enrichments as a result of a close spatial proximity to histone...
  10. .... Collectively, ChIP-PET and ChIP-seq powered by Illumina and other massively parallel tag sequencing platforms have generated and will continue to generate valuable maps of protein factors interacting with genomic DNA in the genomic landscape. From these analyses, general pictures of transcription factor...
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