Latest AI and machine learning research in genetics for healthcare professionals.
Deciphering patterns in the structural and functional anatomy of genes can prove to be very helpful in understanding genetic biology and genomics. Also, the availability of the multiple omics data, along with the advent of machine learning techniques, aids medical professionals in gaining insights about various biological regulations. Gene clustering is one of the many such computation techniques ...
Mosaic variants resulting from postzygotic mutations are prevalent in the human genome and play important roles in human diseases. However, except for cancer-related variants, there is no collection of postzygotic mosaic variants in noncancer disease-related and healthy individuals. Here, we present MosaicBase, a comprehensive database that includes 6698 mosaic variants related to 266 noncancer di...
Treatment planning for pancreas stereotactic body radiation therapy (SBRT) is a difficult and time-consuming task. In this study, we aim to develop a...
Invasive candidiasis is a major challenge to clinical medicine today. However, traditional fungal diagnostic techniques and empirical treatments have ...
The development of Microbial Source Tracking (MST) technologies was borne out of necessity. This was largely due to the: 1) inadequacies of the fecal ...
Improved drug loading content, bioavailability, and controlled release in targeted tissue have been major bottlenecks in the design of precision nanom...
With the development of cancer research, various gene expression datasets containing cancer information show an explosive growth trend. In addition, d...
Gene-gene interaction (G × G) is thought to fill the gap between the estimated heritability of complex diseases and the limited genetic proportion exp...
Autonomous water sampling technologies may help to overcome the human resource challenges of monitoring biological threats to rivers over long time pe...
Until vaccines and effective therapeutics become available, the practical solution to transit safely out of the current coronavirus disease 19 (CoVID-...
BACKGROUND: Uveal melanoma (UM) is the most common primary intraocular malignancy in adults. Monosomy 3 and mutation are strong prognostic factors pr...
Although sequencing a human genome has become affordable, identifying genetic variants from whole-genome sequence data is still a hurdle for researche...
BACKGROUND: The discovery of the CRISPR-Cas9-based gene editing method has opened unprecedented new potential for biological and medical engineering, ...
Vitamin D (VD) levels and several variants in the vitamin D receptor (VDR) gene are associated with the occurrence of diseases of the bones and cartil...
BACKGROUND: Cell-free DNA's (cfDNA) use as a biomarker in cancer is challenging due to genetic heterogeneity of malignancies and rarity of tumor-deriv...
BACKGROUND: Differential expression (DE) analysis of transcriptomic data enables genome-wide analysis of gene expression changes associated with biolo...
Several challenges appear in the application of deep learning to genomic data. First, the dimensionality of input can be orders of magnitude greater t...
Accumulating evidence suggests M2 macrophages contribute to tissue reparation and limit inflammation in multiple sclerosis (MS). However, most studies...
A non-coding RNA (ncRNA) is a kind of RNA that is not converted into protein, however, it is involved in many biological processes, diseases, and canc...
The human telomeric DNA G-quadruplex follows a kinetic partitioning folding mechanism. The underlying folding landscape potentially has many minima se...