Latest AI and machine learning research in genetics for healthcare professionals.
OBJECTIVE: To investigate MRI-based radiomic features in glioma and key genes related to IDH mutations, and to analyze their correlation. METHODS: 61 MRI files from TCIA were divided into training and validation sets (7:3). An external validation set included 66 pathologically confirmed glioma patients. Regions of interest (ROIs) were manually delineated, extracting 1,037 radiomic features. Mann-W...
Selective enrichment of target bacteria from complex communities, such as the human microbiome, has remained a challenge. Here, we report precision single-cell culturomics based on label-free morphology, Raman spectrometry, and Laser-Induced Forward Transfer (LIFT) technology. This approach operates at the level of single microbial cells, many generations before these cells form visible colonies. ...
Conventional intrusion detection systems (IDSs) based on static, signature-based rules are becoming insufficient in response to more advanced, dynamic...
Congenital anomalies of the kidney and urinary tract (CAKUT) are the leading cause of pediatric kidney failure, but predicting individual progression ...
MOTIVATION: In recent years, protein language models (pLMs) and graph neural networks (GNNs) have demonstrated powerful expressive and reasoning capab...
Engineered neutrophils, modified via advanced biotechnological tools, are emerging as pivotal agents in translational medicine. By integrating gene ed...
The diagnosis of endogenous Cushing's syndrome (CS) can be complicated and often delayed, given its low incidence (estimated globally at 1.8 cases to ...
Glioblastoma (GBM) is characterized by profound intratumoral heterogeneity and an immunosuppressive microenvironment that drive therapeutic resistance...
Gene delivery for neurodegenerative cerebral disorders faces formidable structural and practical challenges. The blood-brain, blood- cerebrospinal flu...
BACKGROUND: Accurately identifying somatic variants from genomic sequencing is crucial for understanding and treating cancer. Previously, methods base...
INTRODUCTION: There is a growing demand to make epigenetic aging clocks that are interpretable and actionable. Here, we identify and describe explaina...
Cervical cancer (CC) remains a major global health burden, particularly in low- and middle-income countries (LMICs), where access to timely diagnosis ...
To investigate the potential molecular mechanisms underlying aspartame (APM)-induced malignant phenotypic changes in colorectal cancer (CRC). Candidat...
This study addresses multiple challenges in applying forensic genealogy to Chinese populations by exploring novel kinship classification strategies ba...
Pediatric glioblastoma (pGBM) is an aggressive central nervous system (CNS) tumor whose pathological progression is significantly influenced by exosom...
Wine fermentation remains inherently variable because of the genetic and phenotypic diversity of Saccharomyces cerevisiae and non-Saccharomyces yeasts...
Deep vein thrombosis (DVT) remains difficult to distinguish because of its often silent presentation and the limited specificity of current diagnostic...
Genome-wide association studies (GWAS) have identified numerous disease-associated single nucleotide polymorphisms (SNPs), yet many potential disease-...
Polycystic Ovary Syndrome (PCOS) is a prevalent endocrine and metabolic disorder among reproductive-age women, in which emerging evidence suggests a s...
BACKGROUND: Melanoma is a highly aggressive malignancy with poor clinical outcomes, and endoplasmic reticulum (ER) stress plays an important role in t...