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

Zhaoming Wang; Nilanjan Chatterjee

doi:10.1186/s13059-017-1255-6

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

Zhaoming Wang, Nilanjan Chatterjee

Bloomberg School of Public Health

Research output: Contribution to journal › Article

Abstract

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

Original language	English (US)
Article number	118
Journal	Genome Biology
Volume	18
Issue number	1
DOIs	https://doi.org/10.1186/s13059-017-1255-6
State	Published - Jan 1 2017

ASJC Scopus subject areas

Ecology, Evolution, Behavior and Systematics
Genetics
Cell Biology

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10.1186/s13059-017-1255-6

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Wang, Z., & Chatterjee, N. (2017). Increasing mapping precision of genomewide association studies: To genotype and impute, sequence, or both? Genome Biology, 18(1), [118]. https://doi.org/10.1186/s13059-017-1255-6

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