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Genomic variant annotation workflow for clinical applications
Annotation and interpretation of DNA aberrations identified through next-generation sequencing is becoming an increasingly important task. Even more so in the context of data analysis pipelines for medical applications, where genomic aberrations are associated with phenotypic and clinical features....
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| Foilsithe in: | F1000Res |
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| Main Authors: | , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
F1000Research
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5130070/ https://ncbi.nlm.nih.gov/pubmed/27990260 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.9357.2 |
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