Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases (2023)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s13073-023-01240-0
Publication URI: http://dx.doi.org/10.1186/s13073-023-01240-0
Type: Journal Article/Review
Parent Publication: Genome Medicine
Issue: 1