Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 130

Similar articles for PubMed (Select 22377349)

1.

Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms.

Lu JT, Wang Y, Gibbs RA, Yu F.

Genome Biol. 2012 Feb 29;13(2):R15. doi: 10.1186/gb-2012-13-2-r15.

2.

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.

3.

Assessment of genotype imputation performance using 1000 Genomes in African American studies.

Hancock DB, Levy JL, Gaddis NC, Bierut LJ, Saccone NL, Page GP, Johnson EO.

PLoS One. 2012;7(11):e50610. doi: 10.1371/journal.pone.0050610. Epub 2012 Nov 30.

4.

Genotype imputation for African Americans using data from HapMap phase II versus 1000 genomes projects.

Sung YJ, Gu CC, Tiwari HK, Arnett DK, Broeckel U, Rao DC.

Genet Epidemiol. 2012 Jul;36(5):508-16. doi: 10.1002/gepi.21647. Epub 2012 May 29.

5.

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.

6.

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.

Montgomery SB, Goode DL, Kvikstad E, Albers CA, Zhang ZD, Mu XJ, Ananda G, Howie B, Karczewski KJ, Smith KS, Anaya V, Richardson R, Davis J; 1000 Genomes Project Consortium, MacArthur DG, Sidow A, Duret L, Gerstein M, Makova KD, Marchini J, McVean G, Lunter G.

Genome Res. 2013 May;23(5):749-61. doi: 10.1101/gr.148718.112. Epub 2013 Mar 11.

7.

Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians.

Shen H, Li J, Zhang J, Xu C, Jiang Y, Wu Z, Zhao F, Liao L, Chen J, Lin Y, Tian Q, Papasian CJ, Deng HW.

PLoS One. 2013;8(4):e59494. doi: 10.1371/journal.pone.0059494. Epub 2013 Apr 5.

8.

Imputation-based genomic coverage assessments of current human genotyping arrays.

Nelson SC, Doheny KF, Pugh EW, Romm JM, Ling H, Laurie CA, Browning SR, Weir BS, Laurie CC.

G3 (Bethesda). 2013 Oct 3;3(10):1795-807. doi: 10.1534/g3.113.007161.

9.

Implication of next-generation sequencing on association studies.

Siu H, Zhu Y, Jin L, Xiong M.

BMC Genomics. 2011 Jun 17;12:322. doi: 10.1186/1471-2164-12-322.

10.

Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes.

Bhangale TR, Rieder MJ, Livingston RJ, Nickerson DA.

Hum Mol Genet. 2005 Jan 1;14(1):59-69. Epub 2004 Nov 3.

11.

A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data.

Buchanan CC, Torstenson ES, Bush WS, Ritchie MD.

J Am Med Inform Assoc. 2012 Mar-Apr;19(2):289-94. doi: 10.1136/amiajnl-2011-000652.

12.

Effect of genome-wide genotyping and reference panels on rare variants imputation.

Zheng HF, Ladouceur M, Greenwood CM, Richards JB.

J Genet Genomics. 2012 Oct 20;39(10):545-50. doi: 10.1016/j.jgg.2012.07.002. Epub 2012 Jul 24.

PMID:
23089364
13.

Natural genetic variation caused by small insertions and deletions in the human genome.

Mills RE, Pittard WS, Mullaney JM, Farooq U, Creasy TH, Mahurkar AA, Kemeza DM, Strassler DS, Ponting CP, Webber C, Devine SE.

Genome Res. 2011 Jun;21(6):830-9. doi: 10.1101/gr.115907.110. Epub 2011 Apr 1.

14.

Limitations of the human reference genome for personalized genomics.

Rosenfeld JA, Mason CE, Smith TM.

PLoS One. 2012;7(7):e40294. doi: 10.1371/journal.pone.0040294. Epub 2012 Jul 11.

15.

Genome-wide association study of chronic periodontitis in a general German population.

Teumer A, Holtfreter B, Völker U, Petersmann A, Nauck M, Biffar R, Völzke H, Kroemer HK, Meisel P, Homuth G, Kocher T.

J Clin Periodontol. 2013 Nov;40(11):977-85. doi: 10.1111/jcpe.12154. Epub 2013 Sep 11.

PMID:
24024966
16.

Linkage disequilibrium structure of the 5q31-33 region in a Thai population.

Nuchnoi P, Ohashi J, Naka I, Nacapunchai D, Tokunaga K, Nishida N, Patarapotikul J.

J Hum Genet. 2008;53(9):850-6. doi: 10.1007/s10038-008-0309-8. Epub 2008 Jun 24.

PMID:
18574552
17.

Recent human effective population size estimated from linkage disequilibrium.

Tenesa A, Navarro P, Hayes BJ, Duffy DL, Clarke GM, Goddard ME, Visscher PM.

Genome Res. 2007 Apr;17(4):520-6. Epub 2007 Mar 9.

18.

Imputation across genotyping arrays for genome-wide association studies: assessment of bias and a correction strategy.

Johnson EO, Hancock DB, Levy JL, Gaddis NC, Saccone NL, Bierut LJ, Page GP.

Hum Genet. 2013 May;132(5):509-22. doi: 10.1007/s00439-013-1266-7. Epub 2013 Jan 22.

19.

Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study.

Chen MH, Huang J, Chen WM, Larson MG, Fox CS, Vasan RS, Seshadri S, O'Donnell CJ, Yang Q.

PLoS One. 2012;7(12):e51589. doi: 10.1371/journal.pone.0051589. Epub 2012 Dec 17.

20.

Global similarity with local differences in linkage disequilibrium between the Dutch and HapMap-CEU populations.

Pardo L, Bochdanovits Z, de Geus E, Hottenga JJ, Sullivan P, Posthuma D, Penninx BW, Boomsma D, Heutink P.

Eur J Hum Genet. 2009 Jun;17(6):802-10. doi: 10.1038/ejhg.2008.248. Epub 2009 Jan 7.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk