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Rare variant phasing using paired tumor:normal sequence data
BACKGROUND: In standard high throughput sequencing analysis, genetic variants are not assigned to a homologous chromosome of origin. This process, called haplotype phasing, can reveal information important for understanding the relationship between genetic variants and biological phenotypes. For exa...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537421/ https://www.ncbi.nlm.nih.gov/pubmed/31132991 http://dx.doi.org/10.1186/s12859-019-2753-1 |