Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold.

MOTIVATION: Given the current costs of next-generation sequencing, large studies carry out low-coverage sequencing followed by application of methods that leverage linkage disequilibrium to infer genotypes. We propose a novel method that assumes study samples are sequenced at low coverage and genot...

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Những tác giả chính: Menelaou, A, Marchini, J
Định dạng: Journal article
Ngôn ngữ:English
Được phát hành: 2013

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