Next‐generation sequencing and the evolution of data sharing
Author:
Affiliation:
1. McKusick‐Nathans Department of Genetic Medicine Johns Hopkins University School of Medicine Baltimore Maryland USA
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62239
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1. Japan’s initiative on rare and undiagnosed diseases (IRUD): towards an end to the diagnostic odyssey
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3. PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases
4. The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
5. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
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