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Risk scores arise, scrutinizing cells' nutrient sensors, learning about lncRNAs, and more.

Tests based on millions of common DNA variants reveal hidden disease risk; researchers work to bring them to the clinic

Through “polygenic risk scoring,” researchers can identify people at high risk for disease, even if they don’t present other warning signs; method shows potential for use in the clinic

An inflammation brake, a global hunt for gut microbe diversity, and an algorithm benchmarking tool.

Getting tumor genes out of normal data, marking up the non-coding genome, epileptic variants, and more.

This week: a new angle on an old oncogene, rare variants in common disorders, and molecular hijacking fuels a rare cancer.

A new approach for growing neurons, an HIV survival strategy, whole-genome blood typing, and more.

New research provides insights into the genetic variants that increase risk of Crohn’s disease, as well as other rare diseases