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Next Generation Sequencing and the Future of Genetic Diagnosis
The introduction of next generation sequencing (NGS) has led to an exponential increase of elucidated genetic causes in both extremely rare diseases and common but heterogeneous disorders. It can be applied to the whole or to selected parts of the genome (genome or exome sequencing, gene panels). NG...
Gorde:
| Argitaratua izan da: | Neurotherapeutics |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Springer US
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4391380/ https://ncbi.nlm.nih.gov/pubmed/25052068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-014-0288-8 |
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