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ClinSeK: a targeted variant characterization framework for clinical sequencing
Applying genomics to patient care demands sensitive, unambiguous and rapid characterization of a known set of clinically relevant variants in patients’ samples, an objective substantially different from the standard discovery process, in which every base in every sequenced read must be examined. Fur...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410453/ https://www.ncbi.nlm.nih.gov/pubmed/25918555 http://dx.doi.org/10.1186/s13073-015-0155-1 |