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Fong-Yi Lin

Publications and source records attributed to Fong-Yi Lin.

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GAN-Blot: A Controllable Structure-Style Synthesis Benchmark for Western Blot Forensics

Western blot (WB) images are widely used as key evidence in biomedical research. Recent scientific misconduct cases reveal that WB imagery is increasingly fabricated, making WB forensics a major concern for research integrity. However, while the progress of forensic detection techniques often relies on advances in forgery-generation techniques, the development of WB forensic techniques has been hindered by the lack of standardized appearance attribute definitions, image datasets, and controllable generation frameworks for WB imagery. To address this limitation, we present a controllable WB image synthesis framework, named GAN-Blot, for generating realistic synthetic WB images. We introduce a formulation that decomposes a WB image into a structure component and a style-reference component, enabling independent control over local protein-band geometry and the global visual appearance of a synthetic WB image. GAN-Blot integrates a dual-path autoencoding design with several style-alignment loss terms to enable implicit control over structure-style synthesis without predefined semantic appearance attributes. We further contribute a synthetic WB dataset containing more than 46K images and propose four evaluation protocols for controllable WB synthesis. Extensive experiments show that GAN-Blot can generate WB images with high fidelity in both protein-band structure and visual style. Under blind inspection, the generated images can fool domain experts and are not reliably distinguished from authentic WB images by existing detectors and screening platforms. These results demonstrate their utility as challenging controlled cases for validating and developing WB forensic methods.

cs.CV

Copy-Move Detection in Optical Microscopy: A Segmentation Network and A Dataset

With increasing revelations of academic fraud, detecting forged experimental images in the biomedical field has become a public concern. The challenge lies in the fact that copy-move targets can include background tissue, small foreground objects, or both, which may be out of the training domain and subject to unseen attacks, rendering standard object-detection-based approaches less effective. To address this, we reformulate the problem of detecting biomedical copy-move forgery regions as an intra-image co-saliency detection task and propose CMSeg-Net, a copy-move forgery segmentation network capable of identifying unseen duplicated areas. Built on a multi-resolution encoder-decoder architecture, CMSeg-Net incorporates self-correlation and correlation-assisted spatial-attention modules to detect intra-image regional similarities within feature tensors at each observation scale. This design helps distinguish even small copy-move targets in complex microscopic images from other similar objects. Furthermore, we created a copy-move forgery dataset of optical microscopic images, named FakeParaEgg, using open data from the ICIP 2022 Challenge to support CMSeg-Net's development and verify its performance. Extensive experiments demonstrate that our approach outperforms previous state-of-the-art methods on the FakeParaEgg dataset and other open copy-move detection datasets, including CASIA-CMFD, CoMoFoD, and CMF. The FakeParaEgg dataset, our source code, and the CMF dataset with our manually defined segmentation ground truths available at ``https://github.com/YoursEver/FakeParaEgg''.

eess.IV