As part of the National Institutes of Health's Undiagnosed Diseases Program, researchers had sequenced about 50 exomes from 11 patients and their family members as of last month, as well as full genomes of three individuals. They have so far found disease-causing variants in two patients, and variants likely to be causative in another two.

Researchers find that a personalized medicine approach could help people who experience pain while taking statins, New Scientist reports.

US National Science Foundation is continuing its responsible research conduct training policy despite its flaws, ScienceInsider reports.

A CRISPR-themed meeting explored how the tool could and should be used, Wired reports.

In Science this week: database of proteins' effects on cancer, targeted error correction sequencing, and more.