articleBioinformaticsSep 8, 2011BRONZE OA

A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data

Broad Institute

PubMed
Indexed inarxivcrossrefdoajpubmed

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

1

Topics & keywords

Keywords
  • Imputation (statistics)
  • Genotyping
  • Biology
  • Computational biology
  • Genetics
  • DNA sequencing
  • 1000 Genomes Project
  • Allele frequency
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