Works matching IS 17536561 AND DT 2011 AND VI 5

Results: 1199

Identifying rare variants using a Bayesian regression approach.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S99

By:

Aimin Yan;
Laird, Nan M.;
Cheng Li

Publication type:

Article

Finding genes that influence quantitative traits with tree-based clustering.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S98

By:

Wilson, Ian J.;
Howey, Richard A. J.;
Houniet, Darren T.;
Santibanez-Koref, Mauro

Publication type:

Article

Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S97

By:

Sykes, Jenna;
Lu Cheng;
Wei Xu;
Tsao, Ming-Sound;
Liu, Geoffrey;
Pintilie, Melania

Publication type:

Article

Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S96

By:

Kraja, Aldi T.;
Czajkowski, Jacek;
Feitosa, Mary F.;
Borecki, Ingrid B.;
Province, Michael A.

Publication type:

Article

Search for compound heterozygous effects in exome sequence of unrelated subjects.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S95

By:

Christensen, G. Bryce;
Lambert, Christophe G.

Publication type:

Article

Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S9

By:

Zheng Cai;
Knight, Stacey;
Thomas, Alun;
Camp, Nicola J.

Publication type:

Article

Association tests for rare and common variants based on genotypic and phenotypic measures of similarity between individuals.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S89

By:

Thalamuthu, Anbupalam;
Jingyuan Zhao;
Garrett Teoh Hor Keong;
Kondragunta, Venkateswarlu;
Mukhopadhyay, Indranil

Publication type:

Article

Capability of common SNPs to tag rare variants.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S88

By:

Xiangqing Sun;
Junghyun Namkung;
Xiaofeng Zhu;
Elston, Robert C.

Publication type:

Article

SNP set analysis for detecting disease association using exon sequence data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S91

By:

Ru Wang;
Jie Peng;
Pei Wang

Publication type:

Article

Does pathway analysis make it easier for common variants to tag rare ones?

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S90

By:

Uh, Hae-Won;
Tsonaka, Roula;
Houwing-Duistermaat, Jeanine J.

Publication type:

Article

Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S94

By:

Cherkas, Yauheniya;
Raghavan, Nandini;
Francke, Stephan;
DeFalco, Frank;
Wilcox, Marsha A

Publication type:

Article

Analysis of human mini-exome sequencing data from Genetic Analysis Workshop 17 using a Bayesian hierarchical mixture model.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S93

By:

Filho, Julio S. Bueno;
Morota, Gota;
Tran, Quoc;
Maenner, Matthew J.;
Vera-Cala, Lina M.;
Engelman, Corinne D.;
Meyers, Kristin J.

Publication type:

Article

Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S92

By:

Ayers, Kristin L.;
Mamasoula, Chrysovalanto;
Cordell, Heather J.

Publication type:

Article

Do rare variant genotypes predict common variant genotypes?

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S87

By:

Kent, Jr., Jack W.;
Farook, Vidya;
Göring, Harald H. H.;
Dyer, Thomas D.;
Almasy, Laura;
Duggirala, Ravindranath;
Blangero, John

Publication type:

Article

Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S86

By:

Wenan Chen;
Xi Gao;
Jiexun Wang;
Chuanyu Sun;
Wen Wan;
Degui Zhi;
Nianjun Liu;
Xiangning Chen;
Guimin Gao

Publication type:

Article

Enriching rare variants using family-specific linkage information.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S82

By:

Gang Shi;
Simino, Jeannette;
Rao, Dabeeru C.

Publication type:

Article

Using linkage analysis of large pedigrees to guide association analyses.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S79

By:

Choi, Seung-Hoan;
Chunyu Liu;
Dupuis, Josée;
Logue, Mark W.;
Gyungah Jun

Publication type:

Article

Strategies for selection of subjects for sequencing after detection of a linkage peak.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S77

By:

Allen-Brady, Kristina;
Farnham, James;
Cannon-Albright, Lisa

Publication type:

Article

A pathway-based association analysis model using common and rare variants.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S85

By:

Lu Cheng;
Pingzhao Hu;
Sykes, Jenna;
Pintilie, Melania;
Geoffrey Liu;
Wei Xu

Publication type:

Article

Linkage analysis merging replicate phenotypes: an application to three quantitative phenotypes in two African samples.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S81

By:

Hinrichs, Anthony L.;
Culverhouse, Robert C.;
Suarez, Brian K.

Publication type:

Article

Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S83

By:

Simpson, Claire L.;
Justice, Cristina M.;
Krishnan, Mera;
Wojciechowski, Robert;
Heejong Sung;
Cai, Jerry;
Green, Tiffany;
Lewis, Deyana;
Behneman, Dana;
Wilson, Alexander F.;
Bailey-Wilson, Joan E.

Publication type:

Article

A method to detect single-nucleotide polymorphisms accounting for a linkage signal using covariate-based affected relative pair linkage analysis.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S84

By:

Song, Yeunjoo E.;
Namkung, Junghyun;
Shields, Robert W.;
Baechle, Daniel J.;
Song, Sunah;
Elston, Robert C.

Publication type:

Article

Population structure analysis using rare and common functional variants.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S8

By:

Baye, Tesfaye M.;
Hua He;
Lili Ding;
Kurowski, Brad G.;
Xue Zhang;
Martin, Lisa J.

Publication type:

Article

A novel method to detect rare variants using both family and unrelated case-control data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S80

By:

Tao Feng;
Elston, Robert C.;
Xiaofeng Zhu

Publication type:

Article

Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S76

By:

Akula, Nirmala;
Detera-Wadleigh, Sevilla;
Yin Yao Shugart;
Nalls, Michael;
Steele, Jo;
McMahon, Francis J.

Publication type:

Article

Propensity score analysis in the Genetic Analysis Workshop 17 simulated data set on independent individuals.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S71

By:

Chen Min Lin;
Sathirapongsasuti, Fah J.;
Kerner, Berit

Publication type:

Article

Disease risk prediction with rare and common variants.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S61

By:

Chengqing Wu;
Walsh, Kyle M.;
DeWan, Andrew T.;
Hoh, Josephine;
Zuoheng Wang

Publication type:

Article

A weighted accumulation test for associating rare genetic variation with quantitative phenotypes.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S6

By:

Chuanhua Xing;
Satten, Glen A.;
Allen, Andrew S.

Publication type:

Article

Different approaches for dealing with rare variants in family-based genetic studies: application of a Genetic Analysis Workshop 17 problem.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S78

By:

De Almeida, Marcio Augusto Alfonso;
Vançan Russo Horimoto, Andrea Roseli;
De Oliveira, Paulo Sérgio Lopes;
Krieger, José Eduardo;
Da Costa Pereira, Alexandre

Publication type:

Article

Gene-based multiple trait analysis for exome sequencing data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S75

By:

Jingyuan Zhao;
Anbupalam Thalamuthu

Publication type:

Article

Joint association analysis of bivariate quantitative and qualitative traits.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S74

By:

Mengdie Yuan;
Guoqing Diao

Publication type:

Article

Genetic signal maximization using environmental regression.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S72

By:

Melton, Phillip E.;
Kent, Jr., Jack W.;
Dyer, Thomas D.;
Almasy, Laura;
Blangero, John

Publication type:

Article

Detecting rare functional variants using a wavelet-based test on quantitative and qualitative traits.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S70

By:

Renfang Jiang;
Jianping Dong

Publication type:

Article

Integrating binary traits with quantitative phenotypes for association mapping of multivariate phenotypes.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S73

By:

Mukhopadhyay, Indranil;
Saha, Sujayam;
Ghosh, Saurabh

Publication type:

Article

Using LASSO regression to detect predictive aggregate effects in genetic studies.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S69

By:

Fontanarosa, Joel B.;
Yang Dai

Publication type:

Article

Case-control association testing by graphical modeling for the Genetic Analysis Workshop 17 mini-exome sequence data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S62

By:

Abel, Haley J.;
Thomas, Alun

Publication type:

Article

Methods for detecting associations between phenotype and aggregations of rare variants.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S51

By:

Fan Yang;
Chul Joo Kang;
Marjoram, Paul

Publication type:

Article

A gene-based approach for testing association of rare alleles.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S7

By:

Hongyan Xu;
George, Varghese

Publication type:

Article

Identifying variants that contribute to linkage for dichotomous and quantitative traits in extended pedigrees.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S68

By:

Chen, Wei-Min;
Manichaikul, Ani;
Rich, Stephen S.

Publication type:

Article

Mutational load analysis of unrelated individuals.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S55

By:

Howrigan, Daniel P.;
Simonson, Matthew A.;
Kamens, Helen M.;
Stephens, Sarah H.;
Wills, Amanda G.;
Ehringer, Marissa A.;
Keller, Matthew C.;
McQueen, Matthew B.

Publication type:

Article

Regularized regression method for genome-wide association studies.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S67

By:

Jin Liu;
Kai Wang;
Shuangge Ma;
Jian Huang

Publication type:

Article

Principal components ancestry adjustment for Genetic Analysis Workshop 17 data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S66

By:

Jing Jin;
Cerise, Jane E.;
Sun Jung Kang;
Eun Jung Yoon;
Seungtai Yoon;
Mendell, Nancy R.;
Finch, Stephen J.

Publication type:

Article

Gene-based Higher Criticism methods for largescale exonic single-nucleotide polymorphism data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S65

By:

Shiquan He;
Zheyang Wu

Publication type:

Article

Two-stage study designs combining genomewide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S64

By:

Faye, Laura L.;
Bull, Shelley B.

Publication type:

Article

Power of association tests in the presence of multiple causal variants.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S63

By:

Yanming Di;
Gu Mi;
Luna Sun;
Rongrong Dong;
Hong Zhu;
Lili Peng

Publication type:

Article

Resampling procedures to identify important SNPs using a consensus approach.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S59

By:

Pardy, Christopher;
Motyer, Allan;
Wilson, Susan

Publication type:

Article

Distance-based phenotypic association analysis of DNA sequence data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S54

By:

Doyoung Chung;
Qunyuan Zhang;
Kraja, Aldi T.;
Borecki, Ingrid B.;
Province, Michael A.

Publication type:

Article

Treating phenotype as given: a simple resampling method for genome-wide association studies.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S60

By:

Kai Wang;
Jian Huang

Publication type:

Article

Confidence set of putative quantitative trait loci in whole genome scans with application to the Genetic Analysis Workshop 17 simulated data.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S58

By:

Papachristou, Charalampos

Publication type:

Article

Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S5

By:

Pungpapong, Vitara;
Wang, Libo;
Lin, Yanzhu;
Zhang, Dabao;
Zhang, Min

Publication type:

Article