Dataset Information

Humans represent the precision and utility of information acquired across fixations.

ABSTRACT: Our environment contains an abundance of objects which humans interact with daily, gathering visual information using sequences of eye-movements to choose which object is best-suited for a particular task. This process is not trivial, and requires a complex strategy where task affordance defines the search strategy, and the estimated precision of the visual information gathered from each object may be used to track perceptual confidence for object selection. This study addresses the fundamental problem of how such visual information is metacognitively represented and used for subsequent behaviour, and reveals a complex interplay between task affordance, visual information gathering, and metacogntive decision making. People fixate higher-utility objects, and most importantly retain metaknowledge about how much information they have gathered about these objects, which is used to guide perceptual report choices. These findings suggest that such metacognitive knowledge is important in situations where decisions are based on information acquired in a temporal sequence.

SUBMITTER: Stewart EEM

PROVIDER: S-EPMC8844410 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature

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Humans represent the precision and utility of information acquired across fixations.

Stewart Emma E M EEM Ludwig Casimir J H CJH Schütz Alexander C AC

Scientific reports 20220214 1

Our environment contains an abundance of objects which humans interact with daily, gathering visual information using sequences of eye-movements to choose which object is best-suited for a particular task. This process is not trivial, and requires a complex strategy where task affordance defines the search strategy, and the estimated precision of the visual information gathered from each object may be used to track perceptual confidence for object selection. This study addresses the fundamental ...[more]

PMID: 35165336

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Project description:BackgroundThe decreasing cost of obtaining high-quality calls of genomic variants and the increasing availability of clinically relevant data on such variants are important drivers for personalized oncology. To allow rational genome-based decisions in diagnosis and treatment, clinicians need intuitive access to up-to-date and comprehensive variant information, encompassing, for instance, prevalence in populations and diseases, functional impact at the molecular level, associations to druggable targets, or results from clinical trials. In practice, collecting such comprehensive information on genomic variants is difficult since the underlying data is dispersed over a multitude of distributed, heterogeneous, sometimes conflicting, and quickly evolving data sources. To work efficiently, clinicians require powerful Variant Information Systems (VIS) which automatically collect and aggregate available evidences from such data sources without suppressing existing uncertainty.MethodsWe address the most important cornerstones of modeling a VIS: We take from emerging community standards regarding the necessary breadth of variant information and procedures for their clinical assessment, long standing experience in implementing biomedical databases and information systems, our own clinical record of diagnosis and treatment of cancer patients based on molecular profiles, and extensive literature review to derive a set of design principles along which we develop a relational data model for variant level data. In addition, we characterize a number of public variant data sources, and describe a data integration pipeline to integrate their data into a VIS.ResultsWe provide a number of contributions that are fundamental to the design and implementation of a comprehensive, operational VIS. In particular, we (a) present a relational data model to accurately reflect data extracted from public databases relevant for clinical variant interpretation, (b) introduce a fault tolerant and performant integration pipeline for public variant data sources, and (c) offer recommendations regarding a number of intricate challenges encountered when integrating variant data for clincal interpretation.ConclusionThe analysis of requirements for representation of variant level data in an operational data model, together with the implementation-ready relational data model presented here, and the instructional description of methods to acquire comprehensive information to fill it, are an important step towards variant information systems for genomic medicine.

Dataset Information

Humans represent the precision and utility of information acquired across fixations.

Publications

Humans represent the precision and utility of information acquired across fixations.

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