NEW YORK (GenomeWeb News) – The National Human Genome Research Institute and the National Cancer Institute have awarded four new grants totaling up to $27 million to fund projects that will study the use of genome sequencing in clinical care. The projects will also examine how patients and doctors engage with each other and use such genomic information.

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In PNAS this week: rare variants linked to bleeding disorder, comparison of whole-exome and whole-genome sequencing, and more.

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