Evidence map›Paper›PMID 19486537›Full record

ArticleJournal of biomedical science2009

A novel tool for individual haplotype inference using mixed data.

Chen-Pang Lin, Cathy S J Fann

Abstract read
In one paragraph

Article in Journal of biomedical science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Chen-Pang LinInstitute of Public Health, National Yang-Ming University, Taipei, Taiwan.
Cathy S J Fann

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn many studies, researchers may recruit samples consisting of independent trios and unrelated individuals. However, most of the currently available haplotype inference methods do not cope well with these kinds of mixed data sets.

methodsWe propose a general and simple methodology using a mixture of weighted multinomial (MIXMUL) approach that combines separate haplotype information from unrelated individuals and independent trios for haplotype inference to the individual level.

resultsThe new MIXMUL procedure improves over existing methods in that it can accurately estimate haplotype frequencies from mixed data sets and output probable haplotype pairs in optimized reconstruction outcomes for all subjects that have contributed to estimation. Simulation results showed that this new MIXMUL procedure competes well with the EM-based method, i.e. FAMHAP, under a few assumed scenarios.

conclusionThe results showed that MIXMUL can provide accurate estimates similar to those haplotype frequencies obtained from FAMHAP and output the probable haplotype pairs in the most optimal reconstruction outcome for all subjects that have contributed to estimation. If available data consist of combinations of unrelated individuals and independent trios, the MIXMUL procedure can be used to estimate the haplotype frequencies accurately and output the most likely reconstructed haplotype pairs of each subject in the estimation.

Indexed as

HaplotypesAlgorithmsChromosome MappingComputer SimulationData Interpretation, StatisticalGenetic TechniquesGenome, HumanGenotypeHumansLinkage DisequilibriumModels, GeneticModels, StatisticalModels, TheoreticalReproducibility of Results

Identifiers

PMID19486537
PMCPMC2711065

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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.