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. 2017 Mar 23;169(1):6-12.
doi: 10.1016/j.cell.2017.03.005.

Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research

Affiliations

Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research

Teri A Manolio et al. Cell. .

Abstract

Genome sequencing has revolutionized the diagnosis of genetic diseases. Close collaborations between basic scientists and clinical genomicists are now needed to link genetic variants with disease causation. To facilitate such collaborations, we recommend prioritizing clinically relevant genes for functional studies, developing reference variant-phenotype databases, adopting phenotype description standards, and promoting data sharing.

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Figures

Figure 1
Figure 1
Pathogenicity assertions for 61,169 of 72,472 ClinVar variants as of 9/1/16 (N.B.—no pathogenicity assertions provided for 11,303 variants).

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