PubMed HealthSearch

PubMed · 9509163

Spatial scale interactions and visual-tracking performance.

Abstract

It has previously been observed that low spatial frequencies (< or = 1.0 cycles deg-1) tend to dominate high spatial frequencies (> or = 5.0 cycles deg-1) in several types of visual-information-processing tasks. This earlier work employed reaction times as the primary performance measure and the present experiments address the possibility of low-frequency dominance by evaluating visually guided performance of a completely different response system: the control of slow-pursuit eye movements. Slow-pursuit gains (eye velocity/stimulus velocity) were obtained while observers attempted to track the motion of a sine-wave grating. The drifting gratings were presented on three types of background: a uniform background, a background consisting of a stationary grating, or a flickering background. Low-frequency dominance was evident over a wide range of velocities, in that a stationary high-frequency component produced little disruption in the pursuit of a drifting low spatial frequency, but a stationary low frequency interfered substantially with the tracking of a moving high spatial frequency. Pursuit was unaffected by temporal modulation of the background, suggesting that these effects are due to the spatial characteristics of the stationary grating. Similar asymmetries were observed with respect to the stability of fixation: active fixation was less stable in the presence of a drifting low frequency than in the presence of a drifting high frequency.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

H C Hughes, D M Aronchick, M D Nelson. 1997. Spatial scale interactions and visual-tracking performance.. https://doi.org/10.1068/p261047

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Global Genomic Surveillance.

Global genomic surveillance has emerged as a foundational pillar of public health in the twenty-first century, enabling real-time tracking of pathogen evolution and informing outbreak response. This chapter examines the strategic architecture of global genomic surveillance, focusing on its application to arboviruses such as chikungunya virus (CHIKV). It explores the integration of genomic data with epidemiological, clinical, and environmental information within a One Health framework, while addressing critical challenges in governance, equity, and interoperability. The discussion covers the entire genomic surveillance workflow, from sample collection and sequencing to bioinformatic analysis and phylogenetic inference, and highlights the transformative role of artificial intelligence (AI) in predictive surveillance. By analyzing global initiatives, operational barriers, and emerging technologies, this chapter underscores the necessity of sustainable, equitable, and interoperable genomic systems to proactively address current and future infectious disease threats.

Humans

Systematic Dissection of Key Driver Perturbation Signatures in Single Cells via ECCITE-seq.

CRISPR screens, such as expanded CRISPR-compatible cellular indexing of transcriptomes and epitopes by sequencing (ECCITE-seq), enable the simultaneous measurement of transcriptomes, gRNA identity, and cell-surface protein expression at single-cell resolution to systematically interrogate gene function. This platform provides a powerful and scalable experimental approach for validating disease-associated regulators identified by large-scale association studies and other computational methods, including network-based analyses of multi-omics data. Here, as an example application, we describe an ECCITE-seq framework to characterize the transcriptomic consequences of perturbing multiple neuronal key driver genes associated with Alzheimer's disease (AD) in human-induced pluripotent stem cell (hiPSC)-derived neurons. More broadly, by integrating customized pooled gRNA libraries with different CRISPR effectors across multiple cell types, this approach allows for the assessment of the regulatory impact of candidate genes implicated in development and disease processes.

Humans

Identification of Genome-Wide Chromatin Structural Aberration in Cancer by Hi-C Analysis.

Aberrant three-dimensional genome organization is a hallmark of cancer, often driving oncogene activation through mechanisms such as enhancer hijacking. High-throughput chromosome conformation capture (Hi-C) maps these interactions on a genome-wide scale. Unlike earlier dilution-based methods, in situ Hi-C performs proximity ligation within intact nuclei, minimizing random ligation noise and enabling fine-scale structure detection. This chapter describes an optimized in situ Hi-C protocol tailored for cancer cell lines using MboI digestion and biotin-mediated pull-down to generate high-complexity libraries. We further outline a computational workflow that extends beyond standard topological mapping of compartments and topologically associating domains to identify cancer-specific aberrations. Specifically, we focus on detecting chromosomal rearrangements (structural variants) and characterizing the distinct circular topology of extrachromosomal DNA. This integrated experimental and analytical framework provides the necessary tools to dissect the spatial dysregulation underlying tumor evolution.

Humans