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Use of whole genome sequencing to diagnose a cryptic fusion oncogene
CONTEXT: Whole genome sequencing (WGS) is becoming increasingly available for research purposes, but it has not yet been routinely used for clinical diagnosis. OBJECT: To determine whether whole genome sequencing can identify cryptic, actionable mutations in a clinically relevant time frame. DESIGN,...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2011
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3156695/ https://ncbi.nlm.nih.gov/pubmed/21505136 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jama.2011.497 |
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