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There are 15165 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20645

  2. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20658

  3. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20650

  4. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20657

  5. 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

    Article first published online : 2 OCT 2012, DOI: 10.1002/gepi.21689

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

    Genetic Epidemiology

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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20655

  7. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20659

  8. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20656

  9. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20648

  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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20642

  11. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20647

  12. Effect of linkage disequilibrium on the identification of functional variants

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S115–S119, Alun Thomas, Haley J. Abel, Yanming Di, Laura L. Faye, Jing Jin, Jin Liu, Zheyan Wu and Andrew D. Paterson

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20660

  13. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20649

  14. Multiple testing in high-throughput sequence data: experiences from Group 8 of Genetic Analysis Workshop 17

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S61–S66, Inke R. König, Jeremie Nsengimana, Charalampos Papachristou, Matthew A. Simonson, Kai Wang and Jason A. Weisburd

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20651

  15. 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

    Article first published online : 30 DEC 2013, DOI: 10.1002/gepi.21787

  16. Incorporating biological information into association studies of sequencing data

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S29–S34, Gary Chen, Peng Wei and Anita L. DeStefano

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20646

  17. Simulating Realistic Genomic Data With Rare Variants

    Genetic Epidemiology

    Volume 37, Issue 2, February 2013, Pages: 163–172, Yaji Xu, Yinghua Wu, Chi Song and Heping Zhang

    Article first published online : 17 NOV 2012, DOI: 10.1002/gepi.21696

  18. Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data

    Genetic Epidemiology

    Volume 35, Issue S1, 2011, Pages: S67–S73, Phillip E. Melton and Nathan Pankratz

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20653

  19. 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

    Article first published online : 29 NOV 2011, DOI: 10.1002/gepi.20644

  20. 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

    Article first published online : 19 JUN 2012, DOI: 10.1002/gepi.21649