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Your search keyword '"Danecek, Petr"' showing total 13 results

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13 results on '"Danecek, Petr"'

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1. Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture

2. De novo variants in the RNU4-2snRNA cause a frequent neurodevelopmental syndrome

3. Common genetic variation drives molecular heterogeneity in human iPSCs

4. A global reference for human genetic variation

5. The UK10K project identifies rare variants in health and disease

6. Genetic and chemotherapeutic influences on germline hypermutation.

7. Corrigendum: Common genetic variation drives molecular heterogeneity in human iPSCs

8. An integrated map of genetic variation from 1,092 human genomes

9. Mouse genomic variation and its effect on phenotypes and gene regulation

10. A map of human genome variation from population-scale sequencing

11. Evidence for 28 genetic disorders discovered by combining healthcare and research data.

12. Erratum: Corrigendum: Common genetic variation drives molecular heterogeneity in human iPSCs

13. De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

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