Genome Nexus (1) aggregates variant information from sources that are relevant to cancer research and clinical applications, (2) allows high-performance programmatic access to the aggregated data via ...

Published as an arXiv preprint, the paper details how unsupervised and self-supervised AI models are matching or surpassing ...

Researchers in China developed toGC, a new tool that corrects errors in gene annotations using RNA-seq data. Experimentally validated toGC's accuracy, discovering two novel GPCR genes misannotated as ...

Accurate interpretation of cancer genomics depends on standardized disease classification, tumor characterization, and ...

Insects are a genetically diverse group that interact with humans in various ways—some help feed and clothe us while others can cause diseases or threaten the food supply. It is important that we know ...

SAN DIEGO--(BUSINESS WIRE)--BioBam, a leading bioinformatics solutions provider, proudly presents OmicsBox Version 3.4 at the San Diego Plant and Animal Genome Conference (PAG 32). This latest release ...

In recent years, the development of large-scale sequencing projects has identified numerous genomic variants in the human genome. For instance, the NyuWa genome resource (Cell Reports, 2021), led by ...

DALLAS--(BUSINESS WIRE)--Almaden Genomics has incorporated an end-to-end solution into g.nome™ to process, analyze, and visualize single-cell RNAseq data. A cloud-native platform designed for ...

Genomics is the study of an organism's complete set of genetic material, known as the genome. It involves the sequencing, assembly, and analysis of genomes to understand the structure, function, and ...

Interpretation of genomic variants in tumor samples still presents a challenge in research and the clinical setting. A major issue is that information for variant interpretation is fragmented across ...