Artificial intelligence is rapidly becoming medicine’s most powerful microscope, revealing patterns in human DNA that were ...
Parse Biosciences, the leading provider of scalable and accessible single cell sequencing solutions, today announced a collaboration with Codebreaker Labs to develop and validate a breakthrough ...
A newly revealed molecular tug-of-war may have implications for better understanding how a multitude of diseases and ...
Singlera Genomics, a company focused on the application of novel DNA methylation technologies to genetic diagnosis, with ...
Over the past decades, large-scale human genetic studies have identified numerous risk genes and variants associated with complex diseases and traits.
A newly revealed molecular tug-of-war may have implications for better understanding how a multitude of diseases and ...
Scientists chart a comprehensive cell atlas of the developing human reproductive system, offering new clues into congenital disorders.
Large-scale human genetics studies have shown that many risk variants for common and complex diseases sit in the non-coding ...
A new genetic mapping strategy reveals how entire networks of genes work together to cause disease, filling in the missing ...
The tiny pantheon known as the Asgard archaea bear traits that hint at how plants, animals and fungi emerged on Earth.
TripletDGC links disease genes→cell types→diseases via eQTL-scRNA integration, exposing sparse but critical cell drivers and potential comorbidity ...
This year, gene-editing technology was customized to fix mutations in a single patient’s genes for the first time.