Recently the National Heart, Lung, and Blood Institute reissued an announcement (PAR-15-314) for the Discovery of Genetic Basis of Monogenic Heart, Lung, Blood, and Sleep Disorders (X01). Although funds are not awarded via this resource access award, NHLBI will provide free genome-wide sequencing service to investigators conducting relevant genetic discovery research.
Applications must focus on heart, lung, blood, and sleep disorders likely influenced by genetic variant(s) in a single gene. Complete details are available on the NIH website at www.grants.nih.gov.
