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...

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Detalles Bibliográficos
Autores principales: Buckley, Alexandra R., Ideker, Trey, Carter, Hannah, Schork, Nicholas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Methodology Article
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

Internet

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

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