Researchers have developed a human stem cell model that reveals how genetic mutations cause dangerous fatty tissue buildup in hearts. The findings identify key signaling pathways that could lead to new treatments for this inherited heart condition.
A groundbreaking medical study demonstrates how ultrarapid long-read genome sequencing can provide life-changing genetic diagnoses for ICU patients in under a week. The technology has already enabled immediate treatment adjustments for 64% of diagnosed patients, transforming critical care decision-making.
Medical researchers have implemented a revolutionary diagnostic approach that delivers genetic answers for critically ill patients in record time, according to reports published in the European Journal of Human Genetics. The ultrarapid long-read genome sequencing (LR-GS) pipeline achieved a median turnaround time of just 5.3 days compared to 18.4 days for standard genomic care, potentially transforming outcomes for patients in intensive care units.
Landmark Genome Assembly Reveals Genetic Blueprint of Rare Chinese Pig Breed Scientists have achieved a groundbreaking chromosome-level genome assembly of…
