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There are 114103 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. 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

  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

    Article first published 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

    Article first published 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

    Article first published 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

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

  7. 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

    Article first published online : 26 MAR 2013, DOI: 10.1002/humu.22303

  8. 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

  9. 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

  10. 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

  11. You have free access to this content
    Exploring the association between genetic variation in the SUMO isopeptidase gene USPL1 and breast cancer through integration of data from the population-based GENICA study and external genetic databases

    International Journal of Cancer

    Volume 133, Issue 2, 15 July 2013, Pages: 362–372, Justo Lorenzo Bermejo, Maria Kabisch, Thomas Dünnebier, Sven Schnaidt, Frauke Melchior, Hans-Peter Fischer, Volker Harth, Sylvia Rabstein, Beate Pesch, Thomas Brüning, Christina Justenhoven, Hiltrud Brauch, Christian Baisch, Yon-Dschun Ko and Ute Hamann

    Article first published online : 25 FEB 2013, DOI: 10.1002/ijc.28040

  12. Spectrum of Point Mutations in the Human Genome and Major Subpopulations

    Standard Article

    eLS

    Zhongming Zhao, Huy Vuong and Peilin Jia

    Published Online : 15 MAY 2013, DOI: 10.1002/9780470015902.a0020852.pub2

  13. Simple and Efficient Identification of Rare Recessive Pathologically Important Sequence Variants from Next Generation Exome Sequence Data

    Human Mutation

    Volume 34, Issue 7, July 2013, Pages: 945–952, Ian M. Carr, Joanne Morgan, Christopher Watson, Svitlana Melnik, Christine P. Diggle, Clare V. Logan, Sally M. Harrison, Graham R. Taylor, Sergio D.J. Pena, Alexander F. Markham, Fowzan S. Alkuraya, Graeme C.M. Black, Manir Ali and David T. Bonthron

    Article first published online : 29 APR 2013, DOI: 10.1002/humu.22322

  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. You have full text access to this OnlineOpen article
    How to Include Chromosome X in Your Genome-Wide Association Study

    Genetic Epidemiology

    Volume 38, Issue 2, February 2014, Pages: 97–103, Inke R. König, Christina Loley, Jeanette Erdmann and Andreas Ziegler

    Article first published online : 9 JAN 2014, DOI: 10.1002/gepi.21782

  16. Adjusting for Population Stratification in a Fine Scale With Principal Components and Sequencing Data

    Genetic Epidemiology

    Volume 37, Issue 8, December 2013, Pages: 787–801, Yiwei Zhang, Xiaotong Shen and Wei Pan

    Article first published online : 5 OCT 2013, DOI: 10.1002/gepi.21764

  17. 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

  18. You have full text access to this OnlineOpen article
    Estimating the net contribution of interleukin-28B variation to spontaneous hepatitis C virus clearance

    Hepatology

    Volume 53, Issue 5, May 2011, Pages: 1446–1454, Julia di Iulio, Angela Ciuffi, Karen Fitzmaurice, Dermot Kelleher, Margalida Rotger, Jacques Fellay, Raquel Martinez, Sara Pulit, Hansjakob Furrer, Huldrych F. Günthard, Manuel Battegay, Enos Bernasconi, Patrick Schmid, Bernard Hirschel, Eleanor Barnes, Paul Klenerman, Amalio Telenti, Andri Rauch and and the Swiss HIV Cohort Study

    Article first published online : 22 APR 2011, DOI: 10.1002/hep.24263

  19. Exome Sequencing Identifies Potential Risk Variants for Mendelian Disorders at High Prevalence in Qatar

    Human Mutation

    Volume 35, Issue 1, January 2014, Pages: 105–116, Juan L. Rodriguez-Flores, Khalid Fakhro, Neil R. Hackett, Jacqueline Salit, Jennifer Fuller, Francisco Agosto-Perez, Maey Gharbiah, Joel A. Malek, Mahmoud Zirie, Amin Jayyousi, Ramin Badii, Ajayeb Al-Nabet Al-Marri, Lotfi Chouchane, Dora J. Stadler, Jason G. Mezey and Ronald G. Crystal

    Article first published online : 10 NOV 2013, DOI: 10.1002/humu.22460

  20. Small Insertions Are More Deleterious than Small Deletions in Human Genomes

    Human Mutation

    Volume 34, Issue 12, December 2013, Pages: 1642–1649, Shengfeng Huang, Jie Li, Anlong Xu, Guangrui Huang and Leiming You

    Article first published online : 18 SEP 2013, DOI: 10.1002/humu.22435