Latest AI and machine learning research in genetics for healthcare professionals.
The BiGG Models knowledge base (http://bigg.ucsd.edu) is a centralized repository for high-quality genome-scale metabolic models. For the past 12 years, the website has allowed users to browse and search metabolic models. Within this update, we detail new content and features in the repository, continuing the original effort to connect each model to genome annotations and external databases as wel...
By changing the lifestyle and increasing the cancer incidence, accurate diagnosis becomes a significant medical action. Today, DNA microarray is widely used in cancer diagnosis and screening since it is able to measure gene expression levels. Analyzing them by using common statistical methods is not suitable because of the high gene expression data dimensions. So, this study aims to use new techni...
Ophthalmology has been at the forefront of many innovations in basic science and clinical research. The randomized prospective multicenter clinical tr...
MOTIVATION: Over the past two decades, a circular form of RNA (circular RNA), produced through alternative splicing, has become the focus of scientifi...
MOTIVATION: We expect novel pathogens to arise due to their fast-paced evolution, and new species to be discovered thanks to advances in DNA sequencin...
Protein-related interaction prediction is critical to understanding life processes, biological functions, and mechanisms of drug action. Experimental ...
In recent years, more and more evidence indicates that long non-coding RNA (lncRNA) plays a significant role in the development of complex biological ...
BACKGROUND: Molecular profiling has become essential for tumor risk stratification and treatment selection. However, cancer genome complexity and tech...
BACKGROUND: Bipolar disorder (BD) is a type of chronic emotional disorder with a complex genetic structure. However, its genetic molecular mechanism i...
The integration of multi-modal data, such as histopathological images and genomic data, is essential for understanding cancer heterogeneity and comple...
An immense amount of observable diversity exists for all traits and across global populations. In the post-genomic era, equipped with efficient sequen...
Identification of somatic mutations in tumor tissue is challenged by both technical artifacts, diverse somatic mutational processes, and genetic heter...
A standard strategy to discover somatic mutations in a cancer genome is to use next-generation sequencing (NGS) technologies to sequence the tumor tis...
BACKGROUND: Evidence have increasingly indicated that for human disease, cell metabolism are deeply associated with proteins. Structural mutations and...
BACKGROUND: RNA methylation is a reversible post-transcriptional modification involving numerous biological processes. Ribose 2'-O-methylation is part...
BACKGROUND: Gene Ontology (GO) is a major bioinformatic resource used for analysis of large biomedical datasets, for example from genome-wide associat...
Precision medicine in oncology uses genomic data to provide the right intervention in the right patients at the right time. For this purpose, next-gen...
Congenital heart disease (CHD) is one of the most common birth defects, with complex genetic and environmental etiologies. The reports of genetic vari...
Genome3D consortium is a collaborative project involving protein structure prediction and annotation resources developed by six world-leading structur...
Subcellular localization prediction of the proteome is one of major goals of large-scale genome or proteome sequencing projects to define the gene fun...