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There are 26081 results for: content related to: Introduction to genetic analysis workshop 17 summaries

  1. Quality control issues and the identification of rare functional variants with next-generation sequencing data

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S22–S28, Claudia Hemmelmann, E. Warwick Daw and Alexander F. Wilson

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20645

  2. Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S56–S60, Nathan Tintle, Hugues Aschard, Inchi Hu, Nora Nock, Haitian Wang and Elizabeth Pugh

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20650

  3. Identification of genetic association of multiple rare variants using collapsing methods

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S101–S106, Yan V. Sun, Yun Ju Sung, Nathan Tintle and Andreas Ziegler

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20658

  4. Robust and Powerful Tests for Rare Variants Using Fisher's Method to Combine Evidence of Association From Two or More Complementary Tests

    Genetic Epidemiology

    Volume 37, Issue 1, January 2013, Pages: 110–121, Andriy Derkach, Jerry F. Lawless and Lei Sun

    Version of Record online : 2 OCT 2012, DOI: 10.1002/gepi.21689

  5. Rare variants, common markers: synthetic association and beyond

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S80–S84, Jack W. Kent Jr

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20655

  6. Population-based and family-based designs to analyze rare variants in complex diseases

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S41–S47, Rémi Kazma and Julia N. Bailey

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20648

  7. Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S92–S100, Joan E. Bailey-Wilson, Jennifer S. Brennan, Shelley B. Bull, Robert Culverhouse, Yoonhee Kim, Yuan Jiang, Jeesun Jung, Qing Li, Claudia Lamina, Ying Liu, Reedik Mägi, Yue S. Niu, Claire L. Simpson, Libo Wang, Yildiz E. Yilmaz, Heping Zhang and Zhaogong Zhang

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20657

  8. Detecting Association of Rare and Common Variants by Testing an Optimally Weighted Combination of Variants

    Genetic Epidemiology

    Volume 36, Issue 6, September 2012, Pages: 561–571, Qiuying Sha, Xuexia Wang, Xinli Wang and Shuanglin Zhang

    Version of Record online : 19 JUN 2012, DOI: 10.1002/gepi.21649

  9. Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S85–S91, Rita M. Cantor and Marsha Wilcox

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20656

  10. Brief review of regression-based and machine learning methods in genetic epidemiology: the Genetic Analysis Workshop 17 experience

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S5–S11, Abhijit Dasgupta, Yan V. Sun, Inke R. König, Joan E. Bailey-Wilson and James D. Malley

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20642

  11. You have free access to this content
    The 2015 Annual Meeting of the International Genetic Epidemiology Society

    Genetic Epidemiology

    Volume 39, Issue 7, November 2015, Pages: 529–599,

    Version of Record online : 14 SEP 2015, DOI: 10.1002/gepi.21916

  12. SVSI: Fast and Powerful Set-Valued System Identification Approach to Identifying Rare Variants in Sequencing Studies for Ordered Categorical Traits

    Annals of Human Genetics

    Volume 79, Issue 4, July 2015, Pages: 294–309, Wenjian Bi, Guolian Kang, Yanlong Zhao, Yuehua Cui, Song Yan, Yun Li, Cheng Cheng, Stanley B. Pounds, Michael J. Borowitz, Mary V. Relling, Jun J. Yang, Zhifa Liu, Ching-Hon Pui, Stephen P. Hunger, Christine M. Hartford, Wing Leung and Ji-Feng Zhang

    Version of Record online : 11 MAY 2015, DOI: 10.1111/ahg.12117

  13. A Novel Test for Testing the Optimally Weighted Combination of Rare and Common Variants Based on Data of Parents and Affected Children

    Genetic Epidemiology

    Volume 38, Issue 2, February 2014, Pages: 135–143, Qiuying Sha and Shuanglin Zhang

    Version of Record online : 30 DEC 2013, DOI: 10.1002/gepi.21787

  14. Analysis of exome sequences with and without incorporating prior biological knowledge

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S48–S55, Junghyun Namkung, Paola Raska, Jia Kang, Yunlong Liu, Qing Lu and Xiaofeng Zhu

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20649

  15. Detecting multiple causal rare variants in exome sequence data

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S18–S21, Kenny Q. Ye and Corinne D. Engelman

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20644

  16. Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S107–S114, Alexander F. Wilson and Andreas Ziegler

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20659

  17. Using Reference Databases of Genetic Variation to Evaluate the Potential Pathogenicity of Candidate Disease Variants

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 836–841, Kevin P. Kenna, Russell L. McLaughlin, Orla Hardiman and Daniel G. Bradley

    Version of Record online : 26 MAR 2013, DOI: 10.1002/humu.22303

  18. Local and Global Ancestry Inference and Applications to Genetic Association Analysis for Admixed Populations

    Genetic Epidemiology

    Volume 38, Issue S1, September 2014, Pages: S5–S12, Timothy A. Thornton and Justo Lorenzo Bermejo

    Version of Record online : 11 AUG 2014, DOI: 10.1002/gepi.21819

  19. Dealing with high dimensionality for the identification of common and rare variants as main effects and for gene-environment interaction

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S35–S40, Heike Bickeböller, Jeanine J. Houwing-Duistermaat, Xuefeng Wang and Xiting Yan

    Version of Record online : 29 NOV 2011, DOI: 10.1002/gepi.20647

  20. You have full text access to this OnlineOpen article
    hg19K: addressing a significant lacuna in hg19-based variant calling

    Molecular Genetics & Genomic Medicine

    Volume 5, Issue 1, January 2017, Pages: 15–20, Savita Karthikeyan, Pushpinder S. Bawa and Subhashini Srinivasan

    Version of Record online : 13 NOV 2016, DOI: 10.1002/mgg3.251