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Volume 6 Supplement 1

Genetic Analysis Workshop 14: Microsatellite and single-nucleotide polymorphism


Edited by Joan E Bailey-Wilson, Laura Almasy, Mariza de Andrade, Julia Bailey, Heike Bickeböller, Heather J Cordell, E Warwick Daw, Lynn Goldin, Ellen L Goode, Courtney Gray-McGuire, Wayne Hening, Gail Jarvik, Brion S Maher, Nancy Mendell, Andrew D Paterson, John Rice, Glen Satten, Brian Suarez, Veronica Vieland, Marsha Wilcox, Heping Zhang, Andreas Ziegler and Jean W MacCluer

Genetic Analysis Workshop 14: Microsatellite and single-nucleotide polymorphism. Go to conference site.

Noordwijkerhout, The Netherlands7-10 September 2004

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  1. Content type: Proceedings

    We developed a new marker-reordering algorithm to find the best order of fine-mapping markers for multipoint linkage analysis. The algorithm searches for the best order of fine-mapping markers such that the su...

    Authors: Gyungah Jun, Yeunjoo Song, Sudha K Iyengar and Robert C Elston

    Citation: BMC Genetics 2005 6(Suppl 1):S61

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  2. Content type: Proceedings

    We use the Genetic Analysis Workshop 14 simulated data to explore the effectiveness of a two-stage strategy for mapping complex disease loci consisting of an initial genome scan with confidence interval constr...

    Authors: Juan Pablo Lewinger, Sophia SF Lee, Joanna Biernacka, Long Yang Wu, Haijiang Steven Shi and Shelley B Bull

    Citation: BMC Genetics 2005 6(Suppl 1):S62

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  3. Content type: Proceedings

    There is great interest in the use of computationally intensive methods for fine mapping of marker data. In this paper we develop methods based upon ideas originally proposed 100 years ago in the context of sp...

    Authors: John Molitor, Keyan Zhao and Paul Marjoram

    Citation: BMC Genetics 2005 6(Suppl 1):S63

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  4. Content type: Proceedings

    Bayesian spatial modeling has become important in disease mapping and has also been suggested as a useful tool in genetic fine mapping. We have implemented the Potts model and applied it to the Genetic Analysi...

    Authors: Elena V Moltchanova, Janne Pitkäniemi and Laura Haapala

    Citation: BMC Genetics 2005 6(Suppl 1):S64

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  5. Content type: Proceedings

    It is generally assumed that the detection of disease susceptibility genes via fine-mapping association study is facilitated by consideration of marker haplotypes. In this study, we compared the performance of...

    Authors: Dushanthi Pinnaduwage and Laurent Briollais

    Citation: BMC Genetics 2005 6(Suppl 1):S65

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  6. Content type: Proceedings

    A common dilemma arising in linkage studies of complex genetic diseases is the selection of positive signals, their follow-up with association studies and discrimination between true and false positive results...

    Authors: Neil Shephard, Sally John, Lon Cardon, Mark I McCarthy and Eleftheria Zeggini

    Citation: BMC Genetics 2005 6(Suppl 1):S66

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  7. Content type: Proceedings

    We used the FBAT (family-based association test) software to test for association between 300 individual single-nucleotide polymorphisms and P1 (a latent trait of Kofendred Personality Disorder) in 100 simulat...

    Authors: Ming-Hsi Wang, Mitchell Guo and Yin Y Shugart

    Citation: BMC Genetics 2005 6(Suppl 1):S68

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  8. Content type: Proceedings

    Haplotypes, the combination of closely linked alleles that fall on the same chromosome, show great promise for studying the genetic components of complex diseases. However, when only multilocus genotype data a...

    Authors: Andrew S Allen and Glen A Satten

    Citation: BMC Genetics 2005 6(Suppl 1):S69

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  9. Content type: Proceedings

    We applied a new approach based on Mantel statistics to analyze the Genetic Analysis Workshop 14 simulated data with prior knowledge of the answers. The method was developed in order to improve the power of a ...

    Authors: Lars Beckmann, Christine Fischer, Markus Obreiter, Michael Rabes and Jenny Chang-Claude

    Citation: BMC Genetics 2005 6(Suppl 1):S70

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  10. Content type: Proceedings

    Our goal was to compare methods for tagging single-nucleotide polymorphisms (tagSNPs) with respect to the power to detect disease association under differing haplotype-disease association models. We were also ...

    Authors: Kelly M Burkett, Mercedeh Ghadessi, Brad McNeney, Jinko Graham and Denise Daley

    Citation: BMC Genetics 2005 6(Suppl 1):S71

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  11. Content type: Proceedings

    In genetic association studies, linkage disequilibrium (LD) within a region can be exploited to select a subset of single-nucleotide polymorphisms (SNPs) to genotype with minimal loss of information. A novel e...

    Authors: Joe M Butler, D Timothy Bishop and Jennifer H Barrett

    Citation: BMC Genetics 2005 6(Suppl 1):S72

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  12. Content type: Proceedings

    We compared seven different tagging single-nucleotide polymorphism (SNP) programs in 10 regions with varied amounts of linkage disequilibrium (LD) and physical distance. We used the Collaborative Studies on th...

    Authors: Priya Duggal, Elizabeth M Gillanders, Rasika A Mathias, Grace P Ibay, Alison P Klein, Agnes B Baffoe-Bonnie, Liang Ou, Ian P Dusenberry, Ya-Yu Tsai, Peter S Chines, Betty Q Doan and Joan E Bailey-Wilson

    Citation: BMC Genetics 2005 6(Suppl 1):S73

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  13. Content type: Proceedings

    Haplotype-based methods have become increasingly popular in the last decade because shared lengths in haplotypes can be used for disease localization. In this contribution, we propose a novel linkage-based hap...

    Authors: Andre Kleensang, Daniel Franke, Inke R König and Andreas Ziegler

    Citation: BMC Genetics 2005 6(Suppl 1):S75

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  14. Content type: Proceedings

    We compare and contrast the performance of SIMPLE, a Monte Carlo based software, with that of several other methods for linkage and haplotype analyses, focusing on the simulated data from the New York City pop...

    Authors: Shili Lin, Jie Ding, Crystal Dong, Zhenqiu Liu, Zhenxu J Ma, Shuyan Wan and Yan Xu

    Citation: BMC Genetics 2005 6(Suppl 1):S76

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  15. Content type: Proceedings

    The haplotypes of the X chromosome are accessible to direct count in males, whereas the diplotypes of the females may be inferred knowing the haplotype of their sons or fathers. Here, we investigated: 1) the p...

    Authors: Fabio Marroni, Chiara Toni, Benedetto Pennato, Ya-Yu Tsai, Pryia Duggal, Joan E Bailey-Wilson and Silvano Presciuttini

    Citation: BMC Genetics 2005 6(Suppl 1):S77

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  16. Content type: Proceedings

    Although permutation testing has been the gold standard for assessing significance levels in studies using multiple markers, it is time-consuming. A Bonferroni correction to the nominal p-value that uses the unde...

    Authors: Kristin K Nicodemus, Wenlei Liu, Gary A Chase, Ya-Yu Tsai and M Daniele Fallin

    Citation: BMC Genetics 2005 6(Suppl 1):S78

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