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Increasing mapping precision of genomewide association studies: To genotype and impute, sequence, or both?

Genome Biology (2017) 18(1)
DOI: 10.1186/s13059-017-1255-6
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Abstract

Fine-mapping to identify causal variants in genomewide association studies remains challenging. A recent study provides guidance for future research.

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APA

Wang, Z., & Chatterjee, N. (2017). Increasing mapping precision of genomewide association studies: To genotype and impute, sequence, or both? Genome Biology, 18(1). https://doi.org/10.1186/s13059-017-1255-6

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