Phasing for medical sequencing using rare variants and large haplotype reference panels
<br xmlns:etd="http://www.ouls.ox.ac.uk/ora/modsextensions"><strong>Motivation: </strong>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 datas...
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| Format: | Journal article |
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Oxford University Press
2016
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