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Similar articles for PubMed (Select 21296892)

1.

Using imputed genotypes for relative risk estimation in case-parent studies.

Shi M, London SJ, Chiu GY, Hancock DB, Zaykin D, Weinberg CR.

Am J Epidemiol. 2011 Mar 1;173(5):553-9. doi: 10.1093/aje/kwq363. Epub 2011 Feb 4.

2.

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies.

Hao K, Chudin E, McElwee J, Schadt EE.

BMC Genet. 2009 Jun 16;10:27. doi: 10.1186/1471-2156-10-27.

3.

ATRIUM: testing untyped SNPs in case-control association studies with related individuals.

Wang Z, McPeek MS.

Am J Hum Genet. 2009 Nov;85(5):667-78. doi: 10.1016/j.ajhg.2009.10.006.

4.

Genome-wide association of breast cancer: composite likelihood with imputed genotypes.

Politopoulos I, Gibson J, Tapper W, Ennis S, Eccles D, Collins A.

Eur J Hum Genet. 2011 Feb;19(2):194-9. doi: 10.1038/ejhg.2010.157. Epub 2010 Oct 20.

5.

Evaluation of potential power gain with imputed genotypes in genome-wide association studies.

Becker T, Flaquer A, Brockschmidt FF, Herold C, Steffens M.

Hum Hered. 2009;68(1):23-34. doi: 10.1159/000210446. Epub 2009 Apr 1.

PMID:
19339783
6.

Analysis of untyped SNPs: maximum likelihood and imputation methods.

Hu YJ, Lin DY.

Genet Epidemiol. 2010 Dec;34(8):803-15. doi: 10.1002/gepi.20527.

7.

Comprehensive evaluation of imputation performance in African Americans.

Chanda P, Yuhki N, Li M, Bader JS, Hartz A, Boerwinkle E, Kao WH, Arking DE.

J Hum Genet. 2012 Jul;57(7):411-21. doi: 10.1038/jhg.2012.43. Epub 2012 May 31.

8.

A new statistic to evaluate imputation reliability.

Lin P, Hartz SM, Zhang Z, Saccone SF, Wang J, Tischfield JA, Edenberg HJ, Kramer JR, M Goate A, Bierut LJ, Rice JP; COGA Collaborators COGEND Collaborators, GENEVA.

PLoS One. 2010 Mar 15;5(3):e9697. doi: 10.1371/journal.pone.0009697.

9.

Imputation reliability on DNA biallelic markers for drug metabolism studies.

Mijatovic V, Iacobucci I, Sazzini M, Xumerle L, Mori A, Pignatti PF, Martinelli G, Malerba G.

BMC Bioinformatics. 2012;13 Suppl 14:S7. doi: 10.1186/1471-2105-13-S14-S7. Epub 2012 Sep 7.

10.

Fast and robust association tests for untyped SNPs in case-control studies.

Allen AS, Satten GA, Bray SL, Dudbridge F, Epstein MP.

Hum Hered. 2010;70(3):167-76. doi: 10.1159/000308456. Epub 2010 Jul 30.

11.

Design considerations for genetic linkage and association studies.

Nsengimana J, Bishop DT.

Methods Mol Biol. 2012;850:237-62. doi: 10.1007/978-1-61779-555-8_13.

PMID:
22307702
12.

Imputation of missing single nucleotide polymorphism genotypes using a multivariate mixed model framework.

Calus MP, Veerkamp RF, Mulder HA.

J Anim Sci. 2011 Jul;89(7):2042-9. doi: 10.2527/jas.2010-3297. Epub 2011 Feb 25.

13.

Accuracy of direct genomic values derived from imputed single nucleotide polymorphism genotypes in Jersey cattle.

Weigel KA, de Los Campos G, Vazquez AI, Rosa GJ, Gianola D, Van Tassell CP.

J Dairy Sci. 2010 Nov;93(11):5423-35. doi: 10.3168/jds.2010-3149.

PMID:
20965358
14.

The use of imputed values in the meta-analysis of genome-wide association studies.

Jiao S, Hsu L, Hutter CM, Peters U.

Genet Epidemiol. 2011 Nov;35(7):597-605. doi: 10.1002/gepi.20608. Epub 2011 Jul 18.

15.

GWAF: an R package for genome-wide association analyses with family data.

Chen MH, Yang Q.

Bioinformatics. 2010 Feb 15;26(4):580-1. doi: 10.1093/bioinformatics/btp710. Epub 2009 Dec 29.

16.
17.

The use of family relationships and linkage disequilibrium to impute phase and missing genotypes in up to whole-genome sequence density genotypic data.

Meuwissen T, Goddard M.

Genetics. 2010 Aug;185(4):1441-9. doi: 10.1534/genetics.110.113936. Epub 2010 May 17.

18.

Marker selection for genetic case-control association studies.

Pettersson FH, Anderson CA, Clarke GM, Barrett JC, Cardon LR, Morris AP, Zondervan KT.

Nat Protoc. 2009;4(5):743-52. doi: 10.1038/nprot.2009.38. Epub 2009 Apr 23.

19.

An empirical evaluation of imputation accuracy for association statistics reveals increased type-I error rates in genome-wide associations.

Almeida MA, Oliveira PS, Pereira TV, Krieger JE, Pereira AC.

BMC Genet. 2011 Jan 20;12:10. doi: 10.1186/1471-2156-12-10.

20.

Imputation of missing genotypes from sparse to high density using long-range phasing.

Daetwyler HD, Wiggans GR, Hayes BJ, Woolliams JA, Goddard ME.

Genetics. 2011 Sep;189(1):317-27. doi: 10.1534/genetics.111.128082. Epub 2011 Jul 29.

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