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Träfflista för sökning "WFRF:(Berger Andreas) ;srt2:(2015-2019)"

Sökning: WFRF:(Berger Andreas) > (2015-2019)

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  • Andam, Berima, 1986, et al. (författare)
  • Florida: Feature LOcatIon DAshboard for extracting and visualizing feature traces
  • 2017
  • Ingår i: Proceedings of the Eleventh International Workshop on Variability Modelling of Software-intensive Systems, VaMoS 2017. - New York, NY, USA : ACM. ; Part F126227, s. 100-107
  • Konferensbidrag (refereegranskat)abstract
    • © 2017 Copyright held by the owner/author(s). Features are high-level, domain-specific abstractions over implementation artifacts. Developers use them to communicate and reason about a system, in order to maintain and evolve it. These activities, however, require knowing the locations of features - a common challenge when a system has many developers, many (cloned) variants, or a long lifespan. We believe that embedding feature-location information into software artifacts via annotations eases typical feature-related engineering tasks, such as modifying and removing features, or merging cloned features into a product line. However, regardless of where such annotations stem from - whether embedded by developers when writing code, or retroactively recovered using a feature-location technique - tool support is needed for developers to exploit such annotations. In this tool demonstration, we present a lightweight tool that extracts annotations from software artifacts, aggregates and processes them, and visualizes feature-related information for developers. Views, such as which files implement a specific feature, are presented on different levels of abstraction. Feature metrics, such as feature size, feature scattering, feature tangling, and numbers of feature authors, are also presented. Our tool also incorporates an information-retrieval-based feature-location technique to retroactively recover feature locations.
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  • Frazier-Wood, Alexis C., et al. (författare)
  • Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
  • 2016
  • Ingår i: Nature Genetics. - : Nature Research (part of Springer Nature). - 1061-4036 .- 1546-1718. ; 48, s. 624-
  • Tidskriftsartikel (refereegranskat)abstract
    • Very few genetic variants have been associated with depression and neuroticism, likely because of limitations on sample size in previous studies. Subjective well-being, a phenotype that is genetically correlated with both of these traits, has not yet been studied with genome-wide data. We conducted genome-wide association studies of three phenotypes: subjective well-being (n = 298,420), depressive symptoms (n = 161,460), and neuroticism (n = 170,911). We identify 3 variants associated with subjective well-being, 2 variants associated with depressive symptoms, and 11 variants associated with neuroticism, including 2 inversion polymorphisms. The two loci associated with depressive symptoms replicate in an independent depression sample. Joint analyses that exploit the high genetic correlations between the phenotypes (vertical bar(p) over cap vertical bar approximate to 0.8) strengthen the overall credibility of the findings and allow us to identify additional variants. Across our phenotypes, loci regulating expression in central nervous system and adrenal or pancreas tissues are strongly enriched for association.
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