Evidence map›Paper›PMID 23110720›Full record

ArticleBMC genetics2012

Fast and accurate haplotype frequency estimation for large haplotype vectors from pooled DNA data.

Alexandros Iliadis, Dimitris Anastassiou, Xiaodong Wang

Abstract read
In one paragraph

Article in BMC genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A sequential Monte Carlo framework for haplotype inference in CNV/SNP genotype data.EURASIP journal on bioinformatics & systems biology · 2014
    Article
  5. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Alexandros IliadisCenter for Computational Biology and Bioinformatics and Department of Electrical Engineering, Columbia University, New York, NY, USA.
Dimitris Anastassiou
Xiaodong Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AlgorithmsGene FrequencyHaplotypesDatabases, GeneticDNAGene PoolGenetic MarkersGenome-Wide Association StudyHumansModels, GeneticDNAGenetic Markers

Identifiers

PMID23110720
PMCPMC3560217

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.