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  1. ..., might carry different biologically meaningful information.In the following, we will describe the basic concept of PriOmics and will show that holistic analysis strategies of high-throughput proteomic data have to account for the fact that multiple proteotypic peptides likely represent the same...
  2. ...and ancestry inference. Utilizing feature selection and machine learning methods, HITSNP effectively and reliably screens feature SNPs representing breed diversity from high-throughput data. Furthermore, we have outlined a pipeline for predicting the number and composition of ancestors based on a reference...
  3. ...-term efficacy. Addressing these obstacles is vital for enhancing therapeutic strategies and patient care. Alternative splicing, a post-transcriptional mechanism that enhances transcript diversity (isoforms), can produce proteins with varied functions, cellular localizations, or binding properties. Here, we...
  4. ...in higher eukaryotes, and mutations causing dysregulated splicing underlie a range of genetic diseases. Computational prediction of alternative splicing from genomic sequences not only provides insight into gene-regulatory mechanisms but also helps identify disease-causing mutations and drug targets...
  5. ...identify a diverse class of activity-dependent alternative splicing and describes the temporality and features of its regulation in cultured neurons.Alternative splicing regulates the vast majority of mammalian genes, with >95% of multiexon genes undergoing some form of alternative splicing (Pan et al...
  6. ...to date. Here, we report the construction of a high-throughput CRISPR-Cas9 mutant library for B. mori, a useful resource for silkworm research and breeding. We show its application for gene function interrogation, as well as its potential use for genetic improvement of economic traits. In silkworm...
  7. ...CRISPR-Cas9-based repeat depletion for high-throughput genotyping of complex plant s Marzia Rossato1,2,6, Luca Marcolungo1,6, Luca De Antoni1, Giulia Lopatriello1, Elisa Bellucci3, Gaia Cortinovis3, Giulia Frascarelli3, Laura Nanni3, Elena Bitocchi3, Valerio Di Vittori3, Leonardo Vincenzi1, Filippo...
  8. ...To comprehensively profile alternative polyadenylation across pig tissues, we analyzed 10x Genomics single-nucleus RNA sequencing (10x snRNA-seq) data from our previous study as a preprint on bioRxiv (Chen et al. 2023), which identified 261 cell subtypes spanning 19 distinct pig tissues (Supplemental Table S1...
  9. ..., particularly for variants that induce new or cryptic splice site usage. Here, we present SeqSplice, a high-throughput RNA splicing methodology utilizing barcoded minigene constructs together with a bespoke bioinformatics pipeline for identifying and quantifying the impacts for splice-altering variants. SeqSplice...
  10. ...-to-cell variability of alternative splicing. Here, we present a method, Psix, to confidently identify splicing that changes across a landscape of single cells, using a probabilistic model that is robust against the data limitations of scRNA-seq. Its autocorrelation-inspired approach finds patterns of alternative...
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