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