Abstract

BackgroundTypically, the first phase of a genome wide association study (GWAS) includes genotyping across hundreds of individuals and validation of the most significant SNPs. Allelotyping of pooled genomic DNA is a common approach to reduce the overall cost of the study. Knowledge of haplotype structure can provide additional information to single locus analyses. Several methods have been proposed for estimating haplotype frequencies in a population from pooled DNA data.ResultsWe introduce a technique for haplotype frequency estimation in a population from pooled DNA samples focusing on datasets containing a small number of individuals per pool (2 or 3 individuals) and a large number of markers. We compare our method with the publicly available state-of-the-art algorithms HIPPO and HAPLOPOOL on datasets of varying number of pools and marker sizes. We demonstrate that our algorithm provides improvements in terms of accuracy and computational time over competing methods for large number of markers while demonstrating comparable performance for smaller marker sizes. Our method is implemented in the "Tree-Based Deterministic Sampling Pool" (TDSPool) package which is available for download at http://www.ee.columbia.edu/~anastas/tdspool.ConclusionsUsing a tree-based determinstic sampling technique we present an algorithm for haplotype frequency estimation from pooled data. Our method demonstrates superior performance in datasets with large number of markers and could be the method of choice for haplotype frequency estimation in such datasets.

Highlights

  • The first phase of a genome wide association study (GWAS) includes genotyping across hundreds of individuals and validation of the most significant SNPs

  • For our purposes we have considered only the datasets that had more than 10 SNPs and less than 20 which resulted in selecting a total of 80 blocks

  • We have introduced a new algorithm for estimating haplotype frequencies from pooled DNA samples using a Tree-Based Deterministic sampling scheme

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Summary

Introduction

The first phase of a genome wide association study (GWAS) includes genotyping across hundreds of individuals and validation of the most significant SNPs. Allelotyping of pooled genomic DNA is a common approach to reduce the overall cost of the study. In recent years large genetic association studies involving hundreds or thousands of individuals have become increasingly available, providing opportunities for biological and medical discoveries. In these studies, hundreds of thousands of SNPs are genotyped for the cases and the controls, and discrepancies between the haplotype distributions indicate an association between a genetic region and the disease. The frequency of an allele in each position is given [5]

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