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  1. ..., solving the taxonomic classification problem does not require the full resolution of a locate query. Instead, indexes for taxonomic classification typically support broader queries that either (1) list which in s the query string occurs (“document listing”) or (2) find from which portion of the taxonomic...
  2. ...present an example of combinatorial 109 perturbation response prediction (Figure 1C). The primary inputs to PRIM include a 110 list of genes, a list of perturbation conditions, and the expression profile of an 111 unperturbed cell. The objective is to predict the gene expression profile of this 112...
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  3. ...by enabling more complete capture and interpretation of cytogenetic aberrations with higher resolution and accuracy compared with traditional karyotyping and array-based methods. Methods Ethics approval and consent Ethical approval was given by the regional ethical review board in Stockholm, Sweden (ethical...
  4. ...ORFeome Cloning and Systems Biology: Standardized Mass Production of the Parts From the Parts-List Michael A. Brasch 1 , James L. Hartley 2 , and Marc Vidal 3 , 4 1 Atto Bioscience, Rockville, Maryland 20850, USA 2 SAIC...
  5. ...and brain microglia form a separate, closely related cluster, highlighted in a red box, distinct from other cell types. (C) Module scores based on differentially expressed gene lists and our curated marker list are visualized using a dot plot for the annotated microglia, PVMs, and monocyte clusters...
  6. ...) and 70× faster than SuSiE (∼210 sec). A similar speed advantage was observed on smaller test regions with 1000 variants (ML-MAGES: ∼1 sec; Enet: ∼5 sec; SuSiE: ∼2 sec) (for a full list of times and variance, see Supplemental Table S5). This advantage becomes more significant when analyzing larger...
  7. ...) and their combinations that can direct the desired state transition is crucial for the task. Computational methods have been developed to identify such reprogramming TFs. However, most of them can only generate a ranked list of individual TFs and ignore the identification of TF combinations. Even for individual...
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  9. ...these difficulties, there are existing methods that scan the for possible oligogenic disease combinations. ORVAL accepts a small list of variants as input and provides gene and variant annotations to a predictor that assesses potential oligogenic combinations (Renaux et al. 2019; Versbraegen et al. 2023). Similarly...
  10. ...of nonmetabolic genes. Larger-sized structures are shown in Supplemental Figure 7. A complete list of 28 diverse functional families is provided in Supplemental Table 5.The potential role these FIEs might play in neofunctionalization is given in Supplemental Note 3, which presents evidence for moonlighting...
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