Up to 5% of Americans may carry genetic variants associated with cancer risk, according to a cross-sectional analysis.The ...
Recent advances in genome sequencing have improved all aspects of uncovering the human genome. One of the unlocked areas includes variant calling, or identifying and cataloging genetic variations, ...
Hereditary cancer risk assessment is a rapidly advancing field, driven by the need for comprehensive variant detection, streamlined genomic workflows, and alignment with evolving guidelines. In the UK ...
Variant Bio, a genomics-driven AI drug discovery company, today announced the launch of Inference, the world's first agentic genomic drug dis ...
Rare inherited genetic variants significantly increase familial lung cancer risk, offering new targets for early detection.
Newest Genome Browser features highlight the power of generative AI and machine learning for biology
In the last several years, large language models (LLMs) like ChatGPT and Bard have shown the world the astounding power of generative AI for language creation tools. However, some of the most exciting ...
Genetic inheritance may sound straightforward: One gene causes one trait or a specific illness. When doctors use genetics, it’s usually to try to identify a disease-causing gene to help guide ...
A genetic mutation passed from mother to children in families affected by schizophrenia has now been shown to completely ...
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