Searching journal content for articles similar to Magalhães et al. 28 (7): 1090.

Displaying results 1-10 of 5773
For checked items
  1. ...genotype imputation from LPS data. Among these, Beagle (Browning et al. 2018) and Gencove's loimpute software (Wasik et al. 2021) have been some of the most popular examples. However, they present limitations in scalability for large cohorts and increased computational costs with large reference panels...
  2. ...panels for genotype imputation, which is a fundamental step in genetic analysis and a computationally resource intensive process that requires access to large protected reference panels. It is therefore performed using an outsourcing approach via “imputation servers,” for example, the Michigan Imputation...
  3. ...version: In this window In a new window Figure 1. Overview of Spatial Integration for Imputation and Deconvolution (SIID). Given Xenium and Visium expression matrices AX and AV, respectively, with corresponding gene panels GX and GV (with GX ⊂ GV), and a Xenium to Visium spatial mapping Γ, SIID finds...
  4. ...suitable for laboratories with different resources. Whereas the workflow complexity of PCL-seq is comparable to noncommercial methods such as PIC (Honda et al. 2021) and Light-seq (Kishi et al. 2022), PCL-seq offers broader applicability. (4) Cost-effectiveness and high sensitivity. PCL-seq is highly cost...
  5. ...is a tool and workflow specification that is independent of a particular workflow manager; it aims to increase the portability of scientific workflows by allowing workflows written in CWL to be executed by any CWL-supporting workflow manager. Thus, the tasks of workflow composition and workflow execution...
  6. .... Although pan graphs have helped to reduce reference mapping bias, further performance improvements are possible. We introduce VG-Pedigree, a pedigree-aware workflow based on the pan-mapping tool of Giraffe and the variant calling tool DeepTrio using a specially trained model for Giraffe-based alignments...
  7. ....ResultsOverview of workflowOur goal is to decode CTCs in spatiotemporal specificity throughout human brain development and then uncover disease-relevant cell types for major brain disorders. To this end, we collected various public data sources and conducted a range of bioinformatics and functional genomic analyses (Fig. 1...
  8. ...and for which molecular endophenotypes and complex traits are assessed on the same genotypes. Here, we performed deep RNA sequencing of 200 Drosophila Genetic Reference Panel inbred lines with complete sequences and for which phenotypes of many quantitative traits have been evaluated. We mapped expression...
  9. ...researchers within the team, with only limited internal oversight and critical analysis of the workflow prior to publication. Here, we show how hackathons can be a means of enhancing collaborative science by enabling peer review before results of analyses are published by cross-validating the design...
  10. ...regularization takes advantage of prior knowledge of gene–gene interactions, encouraging pairs of genes with known interactions to be nearby each other in the low-dimensional representation. The resulting matrix factorization imputes gene abundance for both zero and nonzero counts and can be used to cluster...
For checked items

Preprint Server