SPECT in the year 2000: basic principles.

M W Groch; W D Erwin

Home/Archive/PubMed

PubMed · 11142324

SPECT in the year 2000: basic principles.

M W Groch·W D Erwin

View original source ↗Export metadata ↓

Abstract

OBJECTIVE: SPECT has become a routine procedure in most nuclear medicine departments. SPECT provides significant technical challenges for the nuclear medicine technologist, as compared with planar imaging, in the areas of SPECT acquisition, image reconstruction, and data processing. Many new advances in SPECT methodology are becoming available, such as iterative reconstruction, multimodality fusion, and advanced gated cardiac SPECT. SPECT imaging is demanding and requires careful attention to proper acquisition protocols, whether circular or noncircular orbits, and postprocessing is becoming more complex with the addition of iterative reconstruction and attenuation correction algorithms, among others. Understanding the principles of SPECT is essential not only to produce the highest quality scans but also to identify image artifacts. After reading this article, the nuclear medicine technologist should be able to: (a) describe the historical development and benefits of SPECT imaging; (b) state the impact of image matrix size, number of projections, and arc of rotation on final SPECT image quality; (c) discuss the trade-offs between image noise content and spatial and contrast resolution in SPECT reconstruction; (d) discuss SPECT filters and their impact on image quality; (e) explain the differences between filtered backprojection and iterative reconstruction; and (f) describe the impact of attenuation and scatter in SPECT imaging and the advantages and pitfalls of attenuation correction methods.

Explore related subjects

Humans Image Processing, Computer-Assisted Technology, Radiologic Tomography, Emission-Computed, Single-Photon Journal Article

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

M W Groch, W D Erwin. 2000. SPECT in the year 2000: basic principles.. https://pubmed.ncbi.nlm.nih.gov/11142324/

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

KEEP EXPLORING

Related citations

PubMed2027

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↗

PubMed2027

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↗

PubMed2027

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↗