By Andrea Anderson

NEW YORK (GenomeWeb News) – In a study appearing online yesterday in Nature Genetics, investigators from the Wellcome Trust Sanger Institute, the University of Cambridge, and elsewhere used exome sequencing to reveal the compound inheritance patterns behind an autosomal recessive condition called thrombocytopenia with absent radii, or TAR, syndrome.

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In Science this week: the Human Silencing Hub protein complex, and more.

Heads of various research funding agencies discuss how to encourage scientific breakthroughs, ScienceInsider reports.

The Kansas City Star examines issues surrounding newborn genome sequencing.

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