Searching journal content for articles similar to Morrissy et al. 19 (10): 1825.

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  1. ...BX, United Kingdom Corresponding authors: alessio.marcozzi@gmail.com, j.deridder-4@umcutrecht.nlAbstractShallow -wide cell-free DNA sequencing holds great promise for noninvasive cancer monitoring by providing reliable copy number alteration (CNA) and fragmentomic profiles. Single...
  2. ...for Biotechnology, Huntsville, Alabama 35806, USA; 6Department of Medicine, Division of Endocrinology & Metabolism, University of California San Diego, La Jolla, California 92093, USA Corresponding author: agoren@ucsd.eduAbstractChromatin immunoprecipitation followed by sequencing (ChIP-seq) is widely used to study...
  3. ..., Pennsylvania 19104, USA Corresponding authors: montanoc@chop.edu, wtimp@jhu.eduAbstractIn this mini-review, we explore the advancements in -wide DNA methylation profiling, tracing the evolution from traditional methods such as methylation arrays and whole- bisulfite sequencing to the cutting-edge single...
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  4. ...In a new window Figure 1. Coverage of the Y-linked gene kl-3 by raw reads across different sequencing technologies. The three LRS data sets exhibit similar coverage profiles, with two regions of the kl-3 coding sequence (CDS) nearly absent in the raw reads. In contrast, these regions are well represented...
  5. ...studies demonstrated that DNA methylation at transcription factor binding sites (TFBSs) can influence gene expression by regulating the ability of TFs to bind to their target DNA sequences (Kaluscha et al. 2022). These findings demonstrate the fundamental importance of studying the colocalization between...
  6. ..., unlike in tRNAs, m3C sites in poly(A) RNAs are not specifically associated with loop structures.METTL2A downregulates m3C RNAsTo investigate the role of METTL2A in pancreatic cancer cells, we analyzed METTL2A-regulated genes in AsPC-1 cells. Direct RNA sequencing revealed that METTL2A knockdown led...
  7. ...and is expected to improve the interpretation of transcriptomic data in future genomic studies.RNA sequencing (RNA-seq) has become an essential tool for characterizing transcriptomes (Stark et al. 2019), enabling comprehensive profiling of gene expression, including tissue-specific patterns, disease...
  8. ..., hinging on the precise binding of transcription factors (TFs) and cofactors to gene regulatory elements such as promoters and enhancers. Although it is relatively routine to profile -wide DNA binding landscapes of proteins, identifying the specific proteins that bind to, and regulate the transcription of...
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  9. ...diagnoses and treatments based on patients’ genetic and environmental circumstances. A critical component of a person's physiological makeup is their immune system, but individual genetic variation in many immune system genes has remained resistant to analysis using classical whole- or targeted sequencing...
  10. ...private, recurrent, and founder variants. For example, a breast cancer study using nanopore sequencing precisely profiled fourteen variants, ranging from single-exon alterations to whole-gene changes (Dixon et al. 2023). They confirmed a 6126 bp tandem duplication in three samples, and reported a shared 1...
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