Methods for phasing and imputation of very low coverage sequencing data
The introduction of massively parallel short-read sequencing has facilitated rapidly dropping costs of DNA sequencing. This has led to substantial growth in the size of human sequencing projects, with consortia of low coverage sequencing data containing tens of thousands of samples. However, current...
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University of Oxford
2016
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| Online Access: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.724915 |