Evidence map›Paper›PMID 20113476›Full record

ArticleBMC bioinformatics2010

FastTagger: an efficient algorithm for genome-wide tag SNP selection using multi-marker linkage disequilibrium.

Guimei Liu, Yue Wang, Limsoon Wong

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Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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11citing papers in PubMed
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3 · Its place in the literature

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11 citing papers in PubMed.

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5 · Who and what money

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3 authors.

Guimei LiuDepartment of Computer Science, National University of Singapore, Singapore. liugm@comp.nus.edu.sg
Yue Wang
Limsoon Wong

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman genome contains millions of common single nucleotide polymorphisms (SNPs) and these SNPs play an important role in understanding the association between genetic variations and human diseases. Many SNPs show correlated genotypes, or linkage disequilibrium (LD), thus it is not necessary to genotype all SNPs for association study. Many algorithms have been developed to find a small subset of SNPs called tag SNPs that are sufficient to infer all the other SNPs. Algorithms based on the r2 LD statistic have gained popularity because r2 is directly related to statistical power to detect disease associations. Most of existing r2 based algorithms use pairwise LD. Recent studies show that multi-marker LD can help further reduce the number of tag SNPs. However, existing tag SNP selection algorithms based on multi-marker LD are both time-consuming and memory-consuming. They cannot work on chromosomes containing more than 100 k SNPs using length-3 tagging rules.

resultsWe propose an efficient algorithm called FastTagger to calculate multi-marker tagging rules and select tag SNPs based on multi-marker LD. FastTagger uses several techniques to reduce running time and memory consumption. Our experiment results show that FastTagger is several times faster than existing multi-marker based tag SNP selection algorithms, and it consumes much less memory at the same time. As a result, FastTagger can work on chromosomes containing more than 100 k SNPs using length-3 tagging rules.FastTagger also produces smaller sets of tag SNPs than existing multi-marker based algorithms, and the reduction ratio ranges from 3%-9% when length-3 tagging rules are used. The generated tagging rules can also be used for genotype imputation. We studied the prediction accuracy of individual rules, and the average accuracy is above 96% when r2 >/= 0.9.

conclusionsGenerating multi-marker tagging rules is a computation intensive task, and it is the bottleneck of existing multi-marker based tag SNP selection methods. FastTagger is a practical and scalable algorithm to solve this problem.

Indexed as

AlgorithmsSoftwareChromosome MappingDNA Mutational AnalysisGenetic MarkersLinkage DisequilibriumPolymorphism, Single NucleotideGenetic Markers

Identifiers

PMID20113476
PMCPMC3098109

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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.