Literature DB >> 14966673

Incorporating genotyping uncertainty in haplotype inference for single-nucleotide polymorphisms.

Hosung Kang1, Zhaohui S Qin, Tianhua Niu, Jun S Liu.   

Abstract

The accuracy of the vast amount of genotypic information generated by high-throughput genotyping technologies is crucial in haplotype analyses and linkage-disequilibrium mapping for complex diseases. To date, most automated programs lack quality measures for the allele calls; therefore, human interventions, which are both labor intensive and error prone, have to be performed. Here, we propose a novel genotype clustering algorithm, GeneScore, based on a bivariate t-mixture model, which assigns a set of probabilities for each data point belonging to the candidate genotype clusters. Furthermore, we describe an expectation-maximization (EM) algorithm for haplotype phasing, GenoSpectrum (GS)-EM, which can use probabilistic multilocus genotype matrices (called "GenoSpectrum") as inputs. Combining these two model-based algorithms, we can perform haplotype inference directly on raw readouts from a genotyping machine, such as the TaqMan assay. By using both simulated and real data sets, we demonstrate the advantages of our probabilistic approach over the current genotype scoring methods, in terms of both the accuracy of haplotype inference and the statistical power of haplotype-based association analyses.

Entities:  

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Year:  2004        PMID: 14966673      PMCID: PMC1182263          DOI: 10.1086/382284

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  33 in total

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Authors:  J A Douglas; M Boehnke; K Lange
Journal:  Am J Hum Genet       Date:  2000-03-28       Impact factor: 11.025

2.  Detection and integration of genotyping errors in statistical genetics.

Authors:  Eric Sobel; Jeanette C Papp; Kenneth Lange
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3.  High-throughput genotyping with single nucleotide polymorphisms.

Authors:  K Ranade; M S Chang; C T Ting; D Pei; C F Hsiao; M Olivier; R Pesich; J Hebert; Y D Chen; V J Dzau; D Curb; R Olshen; N Risch; D R Cox; D Botstein
Journal:  Genome Res       Date:  2001-07       Impact factor: 9.043

4.  A permutation procedure for the haplotype method for identification of disease-predisposing variants.

Authors:  H Li
Journal:  Ann Hum Genet       Date:  2001-03       Impact factor: 1.670

5.  Utility and accuracy of template-directed dye-terminator incorporation with fluorescence-polarization detection for genotyping single nucleotide polymorphisms.

Authors:  N Akula; Y S Chen; K Hennessy; T G Schulze; G Singh; F J McMahon
Journal:  Biotechniques       Date:  2002-05       Impact factor: 1.993

6.  Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms.

Authors:  Zhaohui S Qin; Tianhua Niu; Jun S Liu
Journal:  Am J Hum Genet       Date:  2002-11       Impact factor: 11.025

7.  High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology.

Authors:  Michael Olivier; Lee-Ming Chuang; Mau-Song Chang; Ying-Tsung Chen; Dee Pei; Koustubh Ranade; Anniek de Witte; Jennifer Allen; Nguyet Tran; David Curb; Richard Pratt; Henk Neefs; Monika de Arruda Indig; Scott Law; Bruce Neri; Lu Wang; David R Cox
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8.  The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models.

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Journal:  Genetics       Date:  1964-01       Impact factor: 4.562

Review 9.  Searching for genetic determinants in the new millennium.

Authors:  N J Risch
Journal:  Nature       Date:  2000-06-15       Impact factor: 49.962

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Journal:  Hypertension       Date:  2003-01       Impact factor: 10.190

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  14 in total

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2.  An algorithm for inferring complex haplotypes in a region of copy-number variation.

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Journal:  Am J Hum Genet       Date:  2008-07-17       Impact factor: 11.025

3.  Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies.

Authors:  Brian L Browning; Zhaoxia Yu
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

Review 4.  Haplotype phasing: existing methods and new developments.

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Journal:  Nat Rev Genet       Date:  2011-09-16       Impact factor: 53.242

5.  Genotype determination for polymorphisms in linkage disequilibrium.

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Journal:  BMC Bioinformatics       Date:  2009-02-20       Impact factor: 3.169

6.  Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingness.

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Journal:  Front Genet       Date:  2012-06-18       Impact factor: 4.599

Review 7.  A comprehensive literature review of haplotyping software and methods for use with unrelated individuals.

Authors:  Rany M Salem; Jennifer Wessel; Nicholas J Schork
Journal:  Hum Genomics       Date:  2005-03       Impact factor: 4.639

8.  Haplotype estimation from fuzzy genotypes using penalized likelihood.

Authors:  Hae-Won Uh; Paul H C Eilers
Journal:  PLoS One       Date:  2011-09-08       Impact factor: 3.240

9.  Inferring haplotypes of copy number variations from high-throughput data with uncertainty.

Authors:  Mamoru Kato; Seungtai Yoon; Naoya Hosono; Anthony Leotta; Jonathan Sebat; Tatsuhiko Tsunoda; Michael Q Zhang
Journal:  G3 (Bethesda)       Date:  2011-06-01       Impact factor: 3.154

10.  A model of higher accuracy for the individual haplotyping problem based on weighted SNP fragments and genotype with errors.

Authors:  Minzhu Xie; Jianxin Wang; Jianer Chen
Journal:  Bioinformatics       Date:  2008-07-01       Impact factor: 6.937

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