A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
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Abstract
MOTIVATION: Most existing methods for DNA sequence analysis rely on accurate sequences or genotypes. However, in applications of the next-generation sequencing (NGS), accurate genotypes may not be easily obtained (e.g. multi-sample low-coverage sequencing or somatic mutation discovery). These applications press for the development of new methods for analyzing sequence data with uncertainty. RESULTS: We present a statistical framework for calling SNPs, discovering somatic mutations, inferring population genetical parameters and performing association tests directly based on sequencing data without explicit genotyping or linkage-based imputation. On real data, we demonstrate that our method achieves comparable…
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Authors
1Topics & keywords
Topics
Keywords
- Imputation (statistics)
- Genotyping
- Biology
- Computational biology
- Genetics
- DNA sequencing
- 1000 Genomes Project
- Allele frequency
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