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 ...

Comprehensive analysis of one of the largest datasets with harmonized variant calls from over 8,000 cancer whole genomes enables researchers worldwide to uncover rare drivers, new targets, and ...

Researchers built an open tool to handle complex genome sequencing data, offering automated quality control, improved variant ...

Inocras, a bioinformatics-led company harnessing the power of whole genome data and proprietary analytics to deliver curated insights, today announced a strategic partnership with NDS Corporation (NDS ...

Expression module in the CGD. A Search by gene ID in the RNA Data module. B Search by range page in the RNA Data module. C visual expression profile page in the RNA Data module. Chrysanthemums—prized ...

Most cancer diagnostics only scratch the surface of the genome, potentially missing key alterations that could transform patient outcomes. A new platform that combines whole-genome sequencing with ...

The National Institute of Health’s database of Genotypes and Phenotypes now includes the genetic data linked to medical information from the Genetic Epidemiology Research on Aging, one of the biggest, ...

The Epstein-Barr virus (EBV) can cause certain types of cancer or autoimmune diseases, but how the body controls this common viral infection is largely unknown. Researchers at the University Hospital ...