Genomes of 100 000 people will be sequenced to create an open access research resource
Author:
Publisher
BMJ
Subject
General Engineering
Cited by 23 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Lost in translation: the pitfalls of Ensembl gene annotations between human genome assemblies and their impact on diagnostics;Expert Review of Molecular Diagnostics;2023-07-19
2. Improved diagnosis of rare disease patients through application of constrained coding region annotation and de novo status;2022-08-19
3. CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank;Cell Genomics;2022-08
4. Genetic data sharing and artificial intelligence in the era of personalized medicine based on a cross‐sectional analysis of the Saudi human genome program;Scientific Reports;2022-01-26
5. CNest: A Novel Copy Number Association Discovery Method Uncovers 862 New Associations from 200,629 Whole Exome Sequence Datasets in the UK Biobank;2021-08-19
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