For Babies with Unknown Diseases, Genome Sequencing Can Deliver a Diagnosis
In new study, researchers show that genome sequencing provides more answers than traditional genetic testing.
In new study, researchers show that genome sequencing provides more answers than traditional genetic testing.
According to physician-scientists at Stanford University, AI tools have already improved healthcare outcomes for some patients.
With a more inclusive reference data set, scientists and doctors will be able to more easily spot clinically relevant genetic variants for all people.
A lesser-known genetic code influences your health—and that of your kids and grandkids.
One major obstacle to precision medicine for all? The cost of sequencing each person’s genome. New sequencing startups could change that.
As the accuracy of traditional cancer screening is called into question, molecular and genetic tests promise an alternative, noninvasive form of early detection.
While working to understand not only his own rare disease but also how the broader healthcare industry develops treatments for rare diseases as a whole, Onno Faber uncovered the building blocks of his new company.
In his latest book, clinical geneticist and biotech entrepreneur Dr. Phil Reilly chronicles centuries of medical progress that have contributed to recent breakthroughs in rare disease medicines, diagnostics, and clinical care. He says we're just...
New studies demonstrate that treating cancer based on its molecular vulnerabilities, rather than where it originated, could translate to better outcomes for patients