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Researcher profile

Jinyang Zhang

Jinyang Zhang contributes to research discovery and scholarly infrastructure.

ResearcherAffiliation not importedOpen to collaborate
Artificial IntelligenceComputer VisionGenomics

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Published work

2 published item(s)

preprint2026arXiv

IConFace: Identity-Structure Asymmetric Conditioning for Unified Reference-Aware Face Restoration

Blind face restoration is highly ill-posed under severe degradation, where identity-critical details may be missing from the degraded input. Same-identity references reduce this ambiguity, but mismatched pose, expression, illumination, age, makeup, or local facial states can lead to overuse of reference appearance. We propose \textbf{IConFace}, a unified reference-aware and no-reference framework with identity--structure asymmetric conditioning. References are distilled into a norm-weighted global AdaFace identity anchor for image-only modulation, while the degraded image is reinforced as the spatial structure anchor through low-rank residuals and block-wise degraded cross-attention with two-route memory. The resulting single checkpoint exploits references when available and falls back to no-reference restoration when absent, improving identity consistency, fine-detail recovery, and degraded-only restoration quality in a unified model.

0 citations0 reviewsNo code linkedOpen access
preprint2021arXiv

RNA-seq data science: From raw data to effective interpretation

RNA-sequencing (RNA-seq) has become an exemplar technology in modern biology and clinical applications over the past decade. It has gained immense popularity in the recent years driven by continuous efforts of the bioinformatics community to develop accurate and scalable computational tools. RNA-seq is a method of analyzing the RNA content of a sample using the modern sequencing platforms. It generates enormous amounts of transcriptomic data in the form of nucleotide sequences, known as reads. RNA-seq analysis enables the probing of genes and corresponding transcripts which is essential for answering important biological questions, such as detecting novel exons, transcripts, gene expressions, and studying alternative splicing structure. However, obtaining meaningful biological signals from raw data using computational methods is challenging due to the limitations of modern sequencing technologies. The need to leverage these technological challenges have pushed the rapid development of many novel computational tools which have evolved and diversified in accordance with technological advancements, leading to the current myriad population of RNA-seq tools. Our review provides a systemic overview of RNA-seq technology and 235 available RNA-seq tools across various domains published from 2008 to 2020, discussing the interdisciplinary nature of bioinformatics involved in RNA sequencing, analysis, and software development.

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