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Items: 1 to 20 of 258

1.

Large genomic region free of GWAS-based common variants contains fertility-related genes.

Qiu R, Chen C, Jiang H, Shen L, Wu M, Liu C.

PLoS One. 2013 Apr 17;8(4):e61917. doi: 10.1371/journal.pone.0061917. Print 2013.

2.

Snat: a SNP annotation tool for bovine by integrating various sources of genomic information.

Jiang J, Jiang L, Zhou B, Fu W, Liu JF, Zhang Q.

BMC Genet. 2011 Oct 7;12:85. doi: 10.1186/1471-2156-12-85.

3.

Segmental duplications in genome-wide significant loci and housekeeping genes; warning for GAPDH and ACTB.

Ghani M, Sato C, Rogaeva E.

Neurobiol Aging. 2013 Jun;34(6):1710.e1-4. doi: 10.1016/j.neurobiolaging.2012.11.006. Epub 2012 Dec 11.

PMID:
23238109
4.

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
5.

Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity.

Waszak SM, Hasin Y, Zichner T, Olender T, Keydar I, Khen M, Stütz AM, Schlattl A, Lancet D, Korbel JO.

PLoS Comput Biol. 2010 Nov 11;6(11):e1000988. doi: 10.1371/journal.pcbi.1000988.

6.
7.

Genome-wide evaluation of the public SNP databases.

Jiang R, Duan J, Windemuth A, Stephens JC, Judson R, Xu C.

Pharmacogenomics. 2003 Nov;4(6):779-89.

PMID:
14596641
8.

Where in the genome are significant single nucleotide polymorphisms from genome-wide association studies located?

Günther T, Schmitt AO, Bortfeldt RH, Hinney A, Hebebrand J, Brockmann GA.

OMICS. 2011 Jul-Aug;15(7-8):507-12. doi: 10.1089/omi.2010.0154. Epub 2011 Jun 23.

PMID:
21699402
9.

Whole genome resequencing of black Angus and Holstein cattle for SNP and CNV discovery.

Stothard P, Choi JW, Basu U, Sumner-Thomson JM, Meng Y, Liao X, Moore SS.

BMC Genomics. 2011 Nov 15;12:559. doi: 10.1186/1471-2164-12-559.

10.

Accuracy of CNV Detection from GWAS Data.

Zhang D, Qian Y, Akula N, Alliey-Rodriguez N, Tang J; Bipolar Genome Study, Gershon ES, Liu C.

PLoS One. 2011 Jan 13;6(1):e14511. doi: 10.1371/journal.pone.0014511.

11.

Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes.

Shen F, Huang J, Fitch KR, Truong VB, Kirby A, Chen W, Zhang J, Liu G, McCarroll SA, Jones KW, Shapero MH.

BMC Genet. 2008 Mar 28;9:27. doi: 10.1186/1471-2156-9-27.

12.

SNP-based pathway enrichment analysis for genome-wide association studies.

Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X.

BMC Bioinformatics. 2011 Apr 15;12:99. doi: 10.1186/1471-2105-12-99.

13.

GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies.

Yu W, Yesupriya A, Wulf A, Hindorff LA, Dowling N, Khoury MJ, Gwinn M.

Eur J Hum Genet. 2011 Oct;19(10):1095-9. doi: 10.1038/ejhg.2011.91. Epub 2011 May 25.

14.

Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.

Bae JS, Cheong HS, Chun JY, Park TJ, Kim JO, Kim EM, Park M, Kim DJ, Lee EJ, Kim EK, Lee JY, Shin HD.

Ophthalmology. 2010 Jul;117(7):1306-12.e4. doi: 10.1016/j.ophtha.2009.11.021. Epub 2010 Mar 3.

PMID:
20202685
15.

Design of tag SNP whole genome genotyping arrays.

Peiffer DA, Gunderson KL.

Methods Mol Biol. 2009;529:51-61. doi: 10.1007/978-1-59745-538-1_4.

PMID:
19381970
16.

A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.

Zhang C, Bailey DK, Awad T, Liu G, Xing G, Cao M, Valmeekam V, Retief J, Matsuzaki H, Taub M, Seielstad M, Kennedy GC.

Bioinformatics. 2006 Sep 1;22(17):2122-8. Epub 2006 Jul 15.

PMID:
16845142
17.

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.

Pani AM, Hobart HH, Morris CA, Mervis CB, Bray-Ward P, Kimberley KW, Rios CM, Clark RC, Gulbronson MD, Gowans GC, Gregg RG.

PLoS One. 2010 Aug 31;5(8):e12349. doi: 10.1371/journal.pone.0012349.

18.

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.

19.

Whole-genome sequencing and genetic variant analysis of a Quarter Horse mare.

Doan R, Cohen ND, Sawyer J, Ghaffari N, Johnson CD, Dindot SV.

BMC Genomics. 2012 Feb 17;13:78. doi: 10.1186/1471-2164-13-78.

20.

INTERSNP: genome-wide interaction analysis guided by a priori information.

Herold C, Steffens M, Brockschmidt FF, Baur MP, Becker T.

Bioinformatics. 2009 Dec 15;25(24):3275-81. doi: 10.1093/bioinformatics/btp596. Epub 2009 Oct 16.

PMID:
19837719

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