Evidence map›Paper›PMID 16259642›Full record

ArticleBMC bioinformatics2005

Selecting additional tag SNPs for tolerating missing data in genotyping.

Yao-Ting Huang, Kui Zhang, Ting Chen, Kun-Mao Chao

Abstract read
In one paragraph

Article in BMC bioinformatics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Yao-Ting HuangDepartment of Computer Science and Information Engineering, National Taiwan University, Taipei, Taiwan. ythuang@acb.csie.ntu.edu.tw
Kui Zhang
Ting Chen
Kun-Mao Chao

Funding

Implications of haplotype structure in the human genomeP50HG002790 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TAVARE, SIMON · 2003 to 2013
$29.9M
NHGRI NIH HHS P50 HG002790
6 · The paper itself

Abstract

backgroundRecent studies have shown that the patterns of linkage disequilibrium observed in human populations have a block-like structure, and a small subset of SNPs (called tag SNPs) is sufficient to distinguish each pair of haplotype patterns in the block. In reality, some tag SNPs may be missing, and we may fail to distinguish two distinct haplotypes due to the ambiguity caused by missing data.

resultsWe show there exists a subset of SNPs (referred to as robust tag SNPs) which can still distinguish all distinct haplotypes even when some SNPs are missing. The problem of finding minimum robust tag SNPs is shown to be NP-hard. To find robust tag SNPs efficiently, we propose two greedy algorithms and one linear programming relaxation algorithm. The experimental results indicate that (1) the solutions found by these algorithms are quite close to the optimal solution; (2) the genotyping cost saved by using tag SNPs can be as high as 80%; and (3) genotyping additional tag SNPs for tolerating missing data is still cost-effective.

conclusionGenotyping robust tag SNPs is more practical than just genotyping the minimum tag SNPs if we can not avoid the occurrence of missing data. Our theoretical analysis and experimental results show that the performance of our algorithms is not only efficient but the solution found is also close to the optimal solution.

Indexed as

Data Interpretation, StatisticalGenotypePolymorphism, Single NucleotideAlgorithmsChromosome MappingComputational BiologyComputer SimulationDatabases, GeneticDNA Mutational AnalysisGene FrequencyGenetic MarkersGenetic Predisposition to DiseaseGenome, HumanHaplotypesHumansModels, GeneticGenetic Markers

Identifiers

PMID16259642
PMCPMC1316880

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LicenceCC BY
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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.