Searching journal content for articles similar to Ghanbari and Ohler 30 (2): 214.

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  1. ..., we used the most deeply sequenced Hi-C data set reported to date: an ultra-deep Hi-C map of human GM12878 lymphoblastoid cells (Harris et al. 2023). The ENCODE Project produced chromatin immunoprecipitation sequencing (ChIP-seq) data for 110 DBPs in this cell line (The ENCODE Project Consortium 2012...
  2. .... On the other hand, the distinct epigenetic hallmarks affect the accessibility and TF and RNA binding preference to DNA of specific genomic regions and introduce distinct GGIs over a similar 1D DNA sequence for different tissues. These interactions are all likely to participate in the establishment of tissue...
  3. .... These auPRCs also show that our neural network approach can indeed outperform related methods on this task.Next, we sought to assess the cross-species performance of another state-of-the-art deep learning model trained on a related TF binding prediction task, distinct from our binary classification setup...
  4. ...identity. A better understanding of how enhancers work will improve the interpretation of noncoding variation and empower the generation of cell type–specific drivers for gene therapy. Here, we explore the combination of deep learning and cross-species chromatin accessibility profiling to build explainable...
  5. ...deep neural networks predict accurately, the principles that they learn are not trivially interpretable as they are in simpler linear models. However, substantial information can be extracted from themodel by examining its parameters, modulating the flow of information through components of the network...
  6. ...IP-seq data for GABPA, the TERT promoter mutation, as well as additional ETS motif gains, can be identified with high confidence. In conclusion, we present a new integrative genomics approach and a deep learning model to identify and interpret functional enhancer mutations with allelic imbalance of chromatin...
  7. ...peptides, which ultimately increases the probability of detecting AEPs and EJPs (see Supplemental Fig. S2). To achieve deep, comprehensive proteome coverage, we used a workflow with multiple fractionation steps designed to decrease sample complexity and increase peptide and protein identification (Fig. 2A...
  8. ...was performed as described (Sanger et al. 1977). Deep sequencing of plasmid DNA was performed on an Illumina NextSeq after purifying plasmid DNA using the Zymoprep yeast plasmid prep II (Zymo Research) and PCR amplification for 12 to 20 cycles.Library selectionCells from the input population were collected...
  9. ...substitutions ill defined. Finally, a recent algorithm based on deep learning (Alipanahi et al. 2015) performed well on a classification task but was not trained in a way that was designed to make quantitative predictions.In view of the above concerns, it is desirable that an algorithm for inferring an accurate...
  10. ...with regulatory potential generally do not allow identification of regulatory targets for individual factors or miRNAs ( Elnitski et al. 2003 ; Taylor et al. 2006 ). Lastly, the comparative prediction of miRNA binding sites in 3′ UTRs proved successful (for reviews, see Lai 2004 ; Rajewsky 2006 ) but has relied...
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