Targeted sequencing on isolates collected in Saudi Arabia led to 16 rare, non-tuberculosis Mycobacterium species from individuals with lung or other infections.
In a cohort of some 300 people with intellectual disability, a genomic approach offered a likely diagnosis some 60 percent of the time.
Along with known contributors to thyroid cancer, researchers detected mutations that were associated with aggressive cases and metastasis.
The Saudi Arabian research team analyzed the autozygomes and exomes of 31 families and found a strong candidate variant in 90 percent of them.
Researchers in Saudi Arabia sequenced the exomes of women having trouble conceiving and found a mutation that appears to halt early embryonic development.
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.