Latest AI and machine learning research in genetics for healthcare professionals.
Visualizing genome organization and transcriptional dynamics with spatial and temporal precision in living cells is essential for elucidating gene regulation and chromatin-associated disease mechanisms, yet conventional methods confront a fundamental tension between endogenous-sequence targeting and live-cell compatibility. Operator-repressor systems require prior insertion of repetitive arrays at...
Despite the power of CRISPR in genome editing, its clinical application is limited by off-target effects; these effects are currently difficult to evaluate at the genome level but are likely to involve chromatin context. Here, we developed the Endogenous Genome-wide Off-target Library Detection (EGOLD) method for high-throughput detection of off-target effects and identification of chromatin conte...
Emerging evidence highlights hypoxia-responsive long non-coding RNAs (lncRNAs) as potential modulators in tumor biology. In this study, we explored th...
The differentiation of species within the genus Geastrum remains a challenging task due to the strong morphological similarity among taxa and the limi...
Genotype-tissue expression profiles are critical for understanding how genetic variation influences gene regulation across tissues, yet they are often...
BACKGROUND: Diabetic foot ulcers (DFUs) represent a severe chronic complication of diabetes and are characterized by persistent impairment of wound he...
Lyme disease (LD), a multifaceted condition caused by Borrelia burgdorferi (Bb), remains poorly understood, particularly regarding metabolic pathways....
BACKGROUND: Accurate grading and prognostic assessment of glioma requires integrating key molecular biomarkers, including IDH mutation status and the ...
BACKGROUND: The gut microbiota adapts to and shapes the host's metabolic state through affecting circulating metabolites and consequent gene regulator...
BACKGROUND: The accurate prediction of cellular responses to perturbations, such as drug treatments, remains a pivotal challenge in single-cell transc...
Advances in next-generation sequencing (NGS) have provided refined insight into bacterial transcriptional regulatory networks (TRNs) on a genome-wide ...
This study presents a novel integrative approach for the analysis of high-dimensional gene expression data, leveraging the complementary strengths of ...
Brucellosis, a neglected zoonosis caused by intracellular Brucella bacteria, remains a formidable global public health challenge, especially in develo...
Cadmium (Cd) is a toxic heavy metal strongly implicated in lung adenocarcinoma (LUAD) through mechanisms involving oxidative stress, epigenetic dysreg...
BACKGROUND: Type 2 diabetes (T2D) is a complex, chronic condition that imposes a substantial burden on health care systems. Prevention and early detec...
Neuro-cancer crosstalk plays an important role in the development and progression of Glioblastoma (GBM), but its specific mechanisms remain incomplete...
BACKGROUND/OBJECTIVE: Stroke remains a leading cause of morbidity and mortality worldwide. Circulating microRNAs (miRNAs) have emerged as promising no...
Identifying plant disease-resistance genes is essential for understanding the plant immune system and accelerating the breeding of disease-resistant c...
BACKGROUND: Esophageal squamous cell carcinoma (ESCC) is a major cause of cancer-related mortality worldwide, with a high prevalence and poor prognosi...
Flat urothelial lesions represent a diagnostically challenging and clinically significant spectrum in bladder pathology. Distinguishing urothelial car...