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PSSV: a novel pattern-based probabilistic approach for somatic structural variation identification
Motivation: Whole genome DNA-sequencing (WGS) of paired tumor and normal samples has enabled the identification of somatic DNA changes in an unprecedented detail. Large-scale identification of somatic structural variations (SVs) for a specific cancer type will deepen our understanding of driver mech...
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| Publicat a: | Bioinformatics |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5254081/ https://ncbi.nlm.nih.gov/pubmed/27659451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw605 |
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