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BSSV: Bayesian based Somatic Structural Variation Identification with Whole Genome DNA-Seq Data
High coverage whole genome DNA-sequencing enables identification of somatic structural variation (SSV) more evident in paired tumor and normal samples. Recent studies show that simultaneous analysis of paired samples provides a better resolution of SSV detection than subtracting shared SVs. However,...
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| Publicat a: | Conf Proc IEEE Eng Med Biol Soc |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4492453/ https://ncbi.nlm.nih.gov/pubmed/25570853 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/EMBC.2014.6944485 |
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