Agilent Technologies has launched ClearSeq AML, a next-generation sequencing-based panel that targets 48 exons in 20 of the most commonly mutated genes in acute myeloid leukemia. Agilent researchers designed the panel in collaboration with Robert Ohgami and Daniel Arber at Stanford University. The panel provides 99.9 percent design coverage of targeted exons, according to the company and is based on its SureSelect and HaloPlex technology.

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Rare gene mutations are guiding the search for drugs to manage chronic pain without opioids, according to CNBC.

The new Francis Crick Institute building can get too noisy for some researchers to concentrate, according to the Guardian.

CBS News reports that there are still many vacancies at the White House Office of Science and Technology Policy, but that it's uncertain whether they will be filled.

In Nucleic Acids Research this week: pipeline to analyze and visualize bacterial genomes, database of global set of human genomes, and more.