Latest AI and machine learning research in genetics for healthcare professionals.
This study investigates forensic ancestry inference in admixed populations using a self-developed 60-DIP panel, analyzing Kyrgyz samples from Northwest China (CNK) and 26 reference populations from the 1000 Genomes Project. Genetic analyses (PCA, ADMIXTURE, TreeMix) indicated that the CNK shares core ancestry with East Asian populations while exhibiting a partially distinct genetic structure, cons...
UNLABELLED: Genetically engineered mouse models (GEMM) of cancer are useful for exploring the development and biological composition of human tumors. Single-cell RNA sequencing (scRNA-seq) provides a transcriptomic snapshot of cancer to explore the heterogeneity of cell states in an immunocompetent context. However, cross-species comparison often suffers from biological batch effect, and inherent ...
UNLABELLED: Single-cell RNA sequencing facilitates the discovery of gene expression signatures that define cell states across patients, which could be...
Single-cell and single-nucleus RNA sequencing are used to reveal heterogeneity in cells, showing a growing potential for precision and personalized me...
Biologically plausible learning mechanisms have implications for understanding brain functions and engineering intelligent systems. Inspired by the mu...
Polymerase chain reaction (PCR) cycle threshold (Ct) values can be used to estimate the viral burden of Severe Acute Respiratory Syndrome Coronavirus ...
Transcriptomic classification methods have been proposed for ovarian clear cell carcinoma. However, their clinical significance and association with p...
Sepsis remains one of the most diagnostically challenging syndromes due to its clinical heterogeneity, overlapping host-pathogen responses, and lack o...
Human tumor organoids represent a paradigm shift in cancer modeling, overcoming critical limitations of conventional systems by faithfully recapitulat...
Widely used in millions of atherosclerosis treatments, conventional metal stents, although pervasive, only provide mechanical support to narrowed arte...
Genome editing with CRISPR-Cas systems is revolutionizing medicine, molecular biology and biotechnology. In this Review, we discuss the contributions ...
RNA-dependent protein assemblies - including the spliceosome, ribosome and RNA-dependent membraneless organelles - have crucial roles in diverse cellu...
The rational design of catalytic nanomaterials, particularly high-entropy alloy (HEA) nanomaterials with their unique structures, is crucial for advan...
BACKGROUND: Pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive cancers, typically diagnosed at an advanced stage due to its su...
BACKGROUND: The expansion of treatment options for prostate cancer (PC) has improved disease-specific and overall survival outcomes but has also raise...
Alzheimer's disease (AD) has a strong genetic predisposition. Genome-wide association studies have identified multiple risk loci, yet many non-coding ...
We present the Chromatin Landscape and Structure to Expression Regressor (CLASTER), an epigenetic-based deep neural network that can integrate differe...
BACKGROUND: Epigenetic modifications play a vital role in the pathogenesis of human diseases, particularly neurodegenerative disorders such as Alzheim...
The advent of CRISPR-based genome editing has revolutionized crop improvement, offering unprecedented precision and efficiency in modifying key agrono...
BACKGROUND: The response of resectable non-small cell lung cancer (NSCLC) to neoadjuvant immunotherapy is heterogeneous. Machine learning can integrat...