Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 28340351.
- Also identified by DOI 10.1016/j.cell.2017.03.005 and PMC identifier 5511379.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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.
Medical subject headings
- Biomedical Research
- Genomics