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A hidden Markov model for haplotype inference for present-absent data of clustered genes using identified haplotypes and haplotype patterns

Overview of attention for article published in Frontiers in Genetics, August 2014
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Title
A hidden Markov model for haplotype inference for present-absent data of clustered genes using identified haplotypes and haplotype patterns
Published in
Frontiers in Genetics, August 2014
DOI 10.3389/fgene.2014.00267
Pubmed ID
Authors

Jihua Wu, Guo-Bo Chen, Degui Zhi, Nianjun Liu, Kui Zhang

Abstract

The majority of killer cell immunoglobin-like receptor (KIR) genes are detected as either present or absent using locus-specific genotyping technology. Ambiguity arises from the presence of a specific KIR gene since the exact copy number (one or two) of that gene is unknown. Therefore, haplotype inference for these genes is becoming more challenging due to such large portion of missing information. Meantime, many haplotypes and partial haplotype patterns have been previously identified due to tight linkage disequilibrium (LD) among these clustered genes thus can be incorporated to facilitate haplotype inference. In this paper, we developed a hidden Markov model (HMM) based method that can incorporate identified haplotypes or partial haplotype patterns for haplotype inference from present-absent data of clustered genes (e.g., KIR genes). We compared its performance with an expectation maximization (EM) based method previously developed in terms of haplotype assignments and haplotype frequency estimation through extensive simulations for KIR genes. The simulation results showed that the new HMM based method outperformed the previous method when some incorrect haplotypes were included as identified haplotypes and/or the standard deviation of haplotype frequencies were small. We also compared the performance of our method with two methods that do not use previously identified haplotypes and haplotype patterns, including an EM based method, HPALORE, and a HMM based method, MaCH. Our simulation results showed that the incorporation of identified haplotypes and partial haplotype patterns can improve accuracy for haplotype inference. The new software package HaploHMM is available and can be downloaded at http://www.soph.uab.edu/ssg/files/People/KZhang/HaploHMM/haplohmm-index.html.

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Mendeley readers

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Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 38%
Student > Master 2 25%
Student > Ph. D. Student 1 13%
Student > Postgraduate 1 13%
Unspecified 1 13%
Other 0 0%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 50%
Biochemistry, Genetics and Molecular Biology 1 13%
Unspecified 1 13%
Social Sciences 1 13%
Engineering 1 13%
Other 0 0%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 12 August 2014.
All research outputs
#20,234,388
of 22,760,687 outputs
Outputs from Frontiers in Genetics
#8,555
of 11,758 outputs
Outputs of similar age
#194,276
of 231,106 outputs
Outputs of similar age from Frontiers in Genetics
#124
of 139 outputs
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