OpenAI releases GPT-5.4, combining reasoning, coding, and computer control in one model, surpassing competitors.
Chennai: One in four Indian breast cancer patients carries inherited genetic variants that raise cancer risk beyond the commonly tested BRCA1 and BRCA.
Researchers screened more than 220,000 single-letter DNA changes, identifying thousands that regulate gene activity in brain, ...
An exome-wide association study of nearly 38,000 smokers from the Mexico City Prospective Study identified rare coding ...
Rapidly testing hundreds of thousands of DNA sequences, scientists identified specific genetic variations contributing to blood pressure, cholesterol, and blood sugar.
A massive genomics effort has identified thousands of single nucleotide non-coding variants, which alter gene activity, that link to disease and health.
Scientists have identified how specific genetic changes function in cells to influence disease risk and other human health ...
Scientists have identified how specific genetic changes function in cells to influence disease risk and other human health traits. By probing regions ...
Background Balanced translocation (BT) carriers have a high risk of recurrent miscarriage and abnormal offspring due to unbalanced gamete production. Clinical genetic testing often fails to detect BTs ...
Genetic studies now identify millions of variants across human populations, yet most disease-associated signals fall outside protein-coding regions. This ...
Combining AI with targeted base editing offers a potentially scalable, cost-effective alternative to traditional CRISPR to decode functional noncoding variants in blood group genes, with direct ...
Background Monogenic disorders are a major cause of fetal structural anomalies. Most genetic diagnoses involve de novo, biallelic or X linked variants; however, inherited variants in autosomal ...
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