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Rare variant phasing using paired tumor:normal sequence data
Abstract 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....
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMC
2019-05-01
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| Edice: | BMC Bioinformatics |
| Témata: | |
| On-line přístup: | http://link.springer.com/article/10.1186/s12859-019-2753-1 |
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