By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – Baylor College of Medicine will use a $6.6 million grant from the National Institutes of Health to lead a research project that will use genetics and genomics technologies to learn more about brittle bone disease.

BCM will work with the University of Washington and the University of California, Los Angeles to study osteogeneis imperfecta, the most common genetic bone disorder, BCM said Monday.

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Magdalena Skipper, the incoming editor-in-chief of Nature, speaks with NPR's Weekend Edition Sunday.

Genetic genealogy has led to an arrest in another cold case, dating back to 1987.

In PLOS this week: mutation in second gene widens clinical symptoms of people with ADD3 mutations, comparative genomic analysis of Pseudovibrio, and more.

Wired reports that 23andMe is trying to bolster its outside collaborations.

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