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Yingwei Tang

Publications and source records attributed to Yingwei Tang.

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DTI: Dynamic Trajectory Initialization for Generative Face Video Super-Resolution

As the most perceptually powerful Face Video Super-Resolution (FVSR) method, existing works in Generative FVSR (GFVSR) mainly exploit the generative prior of pretrained diffusion models. However, viewed as full generation, they suffer from fixed sampling and expensive inference costs if without large-scale auxiliary training. Furthermore, an excessive pursuit of generic perceptual metrics often results in low fidelity. To address these issues, we present Dynamic Trajectory Initialization (DTI) paradigm for GFVSR, which reformulates GFVSR as an input-driven directional restoration. With a novel enhancement-and-injection conditioning mechanism for pretrained DiT backbone, fidelity of our model has been significantly improved without compromising perceptual quality. To dynamically set the starting sampling point, we propose a Discriminative Guide (DG) trained via objective Signal-to-Noise Ratio (SNR) alignment. With only minor model adaptation and fine-tuning, our method achieves a SOTA overall performance across diverse metrics and benchmarks. An analysis of relationship between actual comprehensive quality and common metrics is also conducted, which demonstrates the perception-distortion trade-off and that the LPIPS is the most convincing metric in our case.

cs.CV

Quantum sensing of Lanthandie binding tags with relaxometer of NV center in diamond

Lanthanide binding tags (LBTs) stand out as a prominent group of fluorescent probes that are extensively utilized in biological detection. However, research on LBTs has predominantly emphasized their fluorescence properties, which frequently compromised by background fluorescence noise. Investigating magnetic properties could optimize detection methodologies that offer enhanced sensitivity and specificity. In this study, we measured the response of a relaxometer based on ensemble nitrogen-vacancy (NV) centers in diamond to various amounts of LBTs with gadolinium ions, determining the detection limit of LBTs to be 25 fmol. We then proposed and demonstrated a detection scheme employing the NV relaxometer to detect specific binding between LBTs and target. Specifically, we assessed the relaxometer's response to various concentrations of the interaction between the modified LBTs and Receptor-Binding Domain (RBD) of SARS-COVID-2 spike protein, with the detection threshold reaching ~1 pmol. Our research provides a potential application platform for biomarker detection under picomole concentration by using NV centers to detect the magnetism of LBTs.

quant-ph