ArticleRSC advances2025
Automated fluorescence image stitching for high-throughput and digital microfluidic biosensors.
Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Harnessing microfluidics for microbiology: from bacteria-host interactions to emerging cancer therapies.Communications biology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Fluorescence imaging underpins digital PCR (dPCR), microarrays, and microfluidic biosensors, yet precise image integration remains a technical bottleneck when the sample area exceeds the microscope field of view. Current stitching methods often rely on fiducial markers or manual tuning, limiting automation and robustness, particularly in portable or point-of-care devices. We present a marker-free image stitching algorithm that combines partition-detection-based registration with mask-based illumination correction. The algorithm aligns frames using intrinsic structural features and compensates for brightness inconsistencies in an adaptive manner, without requiring platform-specific parameter tuning. Application to three dPCR systems, including droplet- and chip-based formats, showed an increased number of matched feature points within overlapping regions, improving the reliability of image stitching. In addition, it enhanced intensity uniformity by ≈ 29.6% compared with conventional methods. The proposed algorithm was further validated on microarrays and bead-based chips, demonstrating consistent stitching accuracy and signal integrity across different modalities. This generalized and automation-compatible solution supports high-throughput microfluidic imaging, quantitative bioanalysis, and integration with artificial intelligence-enabled diagnostic workflows.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.