Literature DB >> 19339782

Markov Models for inferring copy number variations from genotype data on Illumina platforms.

Hui Wang1, Jan H Veldink, Hylke Blauw, Leonard H van den Berg, Roel A Ophoff, Chiara Sabatti.   

Abstract

BACKGROUND/AIMS: Illumina genotyping arrays provide information on DNA copy number. Current methodology for their analysis assumes linkage equilibrium across adjacent markers. This is unrealistic, given the markers high density, and can result in reduced specificity. Another limitation of current methods is that they cannot be directly applied to the analysis of multiple samples with the goal of detecting copy number polymorphisms and their association with traits of interest.
METHODS: We propose a new Hidden Markov Model for Illumina genotype data, that takes into account linkage disequilibrium between adjacent loci. Our framework also allows for location specific deletion/duplication rates. When multiple samples are available, we describe a methodology for their analysis that simultaneously reconstructs the copy number states in each sample and identifies genomic locations with increased variability in copy number in the population. This approach can be extended to test association between copy number variants and a disease trait. RESULTS AND
CONCLUSIONS: We show that taking into account linkage disequilibrium between adjacent markers can increase the specificity of a HMM in reconstructing copy number variants, especially single copy deletions. Our multisample approach is computationally practical and can increase the power of association studies. (c) 2009 S. Karger AG, Basel.

Mesh:

Year:  2009        PMID: 19339782      PMCID: PMC2880724          DOI: 10.1159/000210445

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  21 in total

1.  A high-resolution survey of deletion polymorphism in the human genome.

Authors:  Donald F Conrad; T Daniel Andrews; Nigel P Carter; Matthew E Hurles; Jonathan K Pritchard
Journal:  Nat Genet       Date:  2005-12-04       Impact factor: 38.330

2.  Reconstructing genetic ancestry blocks in admixed individuals.

Authors:  Hua Tang; Marc Coram; Pei Wang; Xiaofeng Zhu; Neil Risch
Journal:  Am J Hum Genet       Date:  2006-05-17       Impact factor: 11.025

3.  Spatial smoothing and hot spot detection for CGH data using the fused lasso.

Authors:  Robert Tibshirani; Pei Wang
Journal:  Biostatistics       Date:  2007-05-18       Impact factor: 5.899

4.  PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.

Authors:  Kai Wang; Mingyao Li; Dexter Hadley; Rui Liu; Joseph Glessner; Struan F A Grant; Hakon Hakonarson; Maja Bucan
Journal:  Genome Res       Date:  2007-10-05       Impact factor: 9.043

5.  ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.

Authors:  Michael A van Es; Paul W Van Vught; Hylke M Blauw; Lude Franke; Christiaan G Saris; Peter M Andersen; Ludo Van Den Bosch; Sonja W de Jong; Ruben van 't Slot; Anna Birve; Robin Lemmens; Vianney de Jong; Frank Baas; Helenius J Schelhaas; Kristel Sleegers; Christine Van Broeckhoven; John H J Wokke; Cisca Wijmenga; Wim Robberecht; Jan H Veldink; Roel A Ophoff; Leonard H van den Berg
Journal:  Lancet Neurol       Date:  2007-10       Impact factor: 44.182

6.  Large-scale copy number polymorphism in the human genome.

Authors:  Jonathan Sebat; B Lakshmi; Jennifer Troge; Joan Alexander; Janet Young; Pär Lundin; Susanne Månér; Hillary Massa; Megan Walker; Maoyen Chi; Nicholas Navin; Robert Lucito; John Healy; James Hicks; Kenny Ye; Andrew Reiner; T Conrad Gilliam; Barbara Trask; Nick Patterson; Anders Zetterberg; Michael Wigler
Journal:  Science       Date:  2004-07-23       Impact factor: 47.728

7.  On the statistical analysis of allelic-loss data.

Authors:  M A Newton; M N Gould; C A Reznikoff; J D Haag
Journal:  Stat Med       Date:  1998-07-15       Impact factor: 2.373

8.  Large recurrent microdeletions associated with schizophrenia.

Authors:  Hreinn Stefansson; Dan Rujescu; Sven Cichon; Olli P H Pietiläinen; Andres Ingason; Stacy Steinberg; Ragnheidur Fossdal; Engilbert Sigurdsson; Thordur Sigmundsson; Jacobine E Buizer-Voskamp; Thomas Hansen; Klaus D Jakobsen; Pierandrea Muglia; Clyde Francks; Paul M Matthews; Arnaldur Gylfason; Bjarni V Halldorsson; Daniel Gudbjartsson; Thorgeir E Thorgeirsson; Asgeir Sigurdsson; Adalbjorg Jonasdottir; Aslaug Jonasdottir; Asgeir Bjornsson; Sigurborg Mattiasdottir; Thorarinn Blondal; Magnus Haraldsson; Brynja B Magnusdottir; Ina Giegling; Hans-Jürgen Möller; Annette Hartmann; Kevin V Shianna; Dongliang Ge; Anna C Need; Caroline Crombie; Gillian Fraser; Nicholas Walker; Jouko Lonnqvist; Jaana Suvisaari; Annamarie Tuulio-Henriksson; Tiina Paunio; Timi Toulopoulou; Elvira Bramon; Marta Di Forti; Robin Murray; Mirella Ruggeri; Evangelos Vassos; Sarah Tosato; Muriel Walshe; Tao Li; Catalina Vasilescu; Thomas W Mühleisen; August G Wang; Henrik Ullum; Srdjan Djurovic; Ingrid Melle; Jes Olesen; Lambertus A Kiemeney; Barbara Franke; Chiara Sabatti; Nelson B Freimer; Jeffrey R Gulcher; Unnur Thorsteinsdottir; Augustine Kong; Ole A Andreassen; Roel A Ophoff; Alexander Georgi; Marcella Rietschel; Thomas Werge; Hannes Petursson; David B Goldstein; Markus M Nöthen; Leena Peltonen; David A Collier; David St Clair; Kari Stefansson
Journal:  Nature       Date:  2008-09-11       Impact factor: 49.962

9.  QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.

Authors:  Stefano Colella; Christopher Yau; Jennifer M Taylor; Ghazala Mirza; Helen Butler; Penny Clouston; Anne S Bassett; Anneke Seller; Christopher C Holmes; Jiannis Ragoussis
Journal:  Nucleic Acids Res       Date:  2007-03-06       Impact factor: 16.971

10.  Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms.

Authors:  Sharon J Diskin; Mingyao Li; Cuiping Hou; Shuzhang Yang; Joseph Glessner; Hakon Hakonarson; Maja Bucan; John M Maris; Kai Wang
Journal:  Nucleic Acids Res       Date:  2008-09-10       Impact factor: 16.971

View more
  7 in total

Review 1.  Statistical issues in the analysis of DNA Copy Number Variations.

Authors:  Nathan E Wineinger; Richard E Kennedy; Stephen W Erickson; Mary K Wojczynski; Carl E Bruder; Hemant K Tiwari
Journal:  Int J Comput Biol Drug Des       Date:  2008

2.  RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION.

Authors:  Zhongyang Zhang; Kenneth Lange; Roel Ophoff; Chiara Sabatti
Journal:  Ann Appl Stat       Date:  2010-12-01       Impact factor: 2.083

3.  EnsembleCNV: an ensemble machine learning algorithm to identify and genotype copy number variation using SNP array data.

Authors:  Zhongyang Zhang; Haoxiang Cheng; Xiumei Hong; Antonio F Di Narzo; Oscar Franzen; Shouneng Peng; Arno Ruusalepp; Jason C Kovacic; Johan L M Bjorkegren; Xiaobin Wang; Ke Hao
Journal:  Nucleic Acids Res       Date:  2019-04-23       Impact factor: 16.971

4.  Reconstructing DNA copy number by joint segmentation of multiple sequences.

Authors:  Zhongyang Zhang; Kenneth Lange; Chiara Sabatti
Journal:  BMC Bioinformatics       Date:  2012-08-16       Impact factor: 3.169

5.  VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions.

Authors:  Jianxin Shi; Xiaohong R Yang; Neil E Caporaso; Maria T Landi; Peng Li
Journal:  Front Genet       Date:  2014-03-18       Impact factor: 4.599

6.  Frequency of KLK3 gene deletions in the general population.

Authors:  Santiago Rodriguez; Osama A Al-Ghamdi; Philip Ai Guthrie; Hashem A Shihab; Wendy McArdle; Tom Gaunt; Khalid K Alharbi; Ian Nm Day
Journal:  Ann Clin Biochem       Date:  2016-08-23       Impact factor: 2.057

7.  A method for calling copy number polymorphism using haplotypes.

Authors:  Gun Ho Jang; Jason D Christie; Rui Feng
Journal:  Front Genet       Date:  2013-09-23       Impact factor: 4.599

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.