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Phasing for medical sequencing using rare variants and large haplotype reference panels
Motivation: There is growing recognition that estimating haplotypes from high coverage sequencing of single samples in clinical settings is an important problem. At the same time very large datasets consisting of tens and hundreds of thousands of high-coverage sequenced samples will soon be availabl...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4920110/ https://ncbi.nlm.nih.gov/pubmed/27153703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw065 |
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