# Fast Spot Locating for Low-Density DNA Microarray

**Authors:** MinGin Kim, Jongwon Kim, Sun-Hee Kim, Jong-Dae Kim

PMC · DOI: 10.3390/s25072135 · 2025-03-28

## TL;DR

This paper introduces a fast and efficient method for locating spots on low-density DNA microarrays, improving speed and performance for diagnostic use.

## Contribution

The novel approach combines template matching with vectorized programming and square templates to significantly speed up spot localization.

## Key findings

- Vectorized programming accelerated key calculations by 82 times on a PC and 6000 times on a Raspberry Pi.
- Square templates reduced processing time by fourfold without affecting detection accuracy.
- The method was validated on HPV genotyping images, showing robust performance in real-world clinical settings.

## Abstract

Low-density DNA microarrays are crucial in molecular diagnostics due to their cost-effectiveness and high sensitivity. However, reliable spot localization remains challenging due to positional variations and image artifacts. Traditional intensity-based methods often struggle with weak fluorescence signals. To address this, we propose a rapid spot localization method that combines template matching with point pattern matching, enhanced through vectorized programming and square (box) templates. Vectorized programming accelerated the most time-consuming calculation by 82 times on a PC and was 6000 times faster on a Raspberry Pi compared to a for-loop implementation. While this improvement applies to the vectorized square calculation alone, substantial performance gains were still achieved in the overall process. Additionally, replacing circular templates with square templates resulted in a fourfold reduction in processing time without compromising detection performance. The proposed method effectively reduces computational overhead, making it suitable for high-throughput and resource-constrained applications. The method was validated using HPV genotyping images from commercial DNA microarrays, demonstrating its practical applicability and robust performance in clinical settings.

## Full-text entities

- **Genes:** HBB (hemoglobin subunit beta) [NCBI Gene 3043] {aka CD113t-C, ECYT6, beta-globin}
- **Diseases:** beta-thalassemia (MESH:D017086), injury to (MESH:D014947), cervical cancer (MESH:D002583), infectious disease (MESH:D003141), colorectal cancer (MESH:D015179)
- **Chemicals:** Cy5 (MESH:C085321), dUTP (MESH:C027078)
- **Species:** Neisseria gonorrhoeae (species) [taxon 485], Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11991467/full.md

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Source: https://tomesphere.com/paper/PMC11991467