Literature DB >> 18651098

New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations.

Kazuharu Misawa1, Shoogo Fujii2,3, Toshimasa Yamazaki2, Atsushi Takahashi2, Junichi Takasaki2, Masao Yanagisawa3, Yozo Ohnishi4, Yusuke Nakamura5, Naoyuki Kamatani2,6.   

Abstract

The multiple comparison problem arises in population-based studies when the association between phenotypes and multilocus genotypes is examined. Although Bonferroni's correction is often used to cope with such a problem, it may yield too conservative conclusions because all of the tests are assumed to be independent. We have developed new correction algorithms for the test of independence between phenotypes and multilocus genotypes at loci in linkage disequilibrium. In one of the algorithms, the exact type I error rate is calculated for the independency test. We found that such exact probabilities can be calculated using a 128 CPU PC cluster if the numbers of cases and controls are not more than 50. As an alternative method, we developed algorithms to calculate asymptotically the type I error rates using a Markov-chain Monte Carlo sampler that provided a good approximation to values calculated by the exact method. When the new algorithms were applied to both simulation and real data, the real overall type I error rates for the loci in linkage disequilibrium were from one-third to half as high as those obtained by Bonferroni's correction. These algorithms are likely to be useful for multilocus association studies for data obtained by case-control and cohort studies.

Mesh:

Year:  2008        PMID: 18651098     DOI: 10.1007/s10038-008-0312-0

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  25 in total

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Authors:  Y Ohnishi; T Tanaka; K Ozaki; R Yamada; H Suzuki; Y Nakamura
Journal:  J Hum Genet       Date:  2001       Impact factor: 3.172

2.  Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed with haplotype-tagging SNPs.

Authors:  Naoyuki Kamatani; Akihiro Sekine; Takuya Kitamoto; Aritoshi Iida; Susumu Saito; Akifumi Kogame; Eisuke Inoue; Manabu Kawamoto; Masayoshi Harigai; Yusuke Nakamura
Journal:  Am J Hum Genet       Date:  2004-06-16       Impact factor: 11.025

3.  A powerful strategy to account for multiple testing in the context of haplotype analysis.

Authors:  Tim Becker; Michael Knapp
Journal:  Am J Hum Genet       Date:  2004-07-30       Impact factor: 11.025

4.  A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other.

Authors:  Dale R Nyholt
Journal:  Am J Hum Genet       Date:  2004-03-02       Impact factor: 11.025

5.  Rapid simulation of P values for product methods and multiple-testing adjustment in association studies.

Authors:  S R Seaman; B Müller-Myhsok
Journal:  Am J Hum Genet       Date:  2005-01-11       Impact factor: 11.025

6.  Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results.

Authors:  E Lander; L Kruglyak
Journal:  Nat Genet       Date:  1995-11       Impact factor: 38.330

7.  Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.

Authors:  Kouichi Ozaki; Yozo Ohnishi; Aritoshi Iida; Akihiko Sekine; Ryo Yamada; Tatsuhiko Tsunoda; Hiroshi Sato; Hideyuki Sato; Masatsugu Hori; Yusuke Nakamura; Toshihiro Tanaka
Journal:  Nat Genet       Date:  2002-11-11       Impact factor: 38.330

8.  An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis.

Authors:  Hideki Kizawa; Ikuyo Kou; Aritoshi Iida; Akihiro Sudo; Yoshinari Miyamoto; Akira Fukuda; Akihiko Mabuchi; Akihiro Kotani; Akira Kawakami; Seizo Yamamoto; Atsumasa Uchida; Kozo Nakamura; Kohei Notoya; Yusuke Nakamura; Shiro Ikegawa
Journal:  Nat Genet       Date:  2005-01-09       Impact factor: 38.330

9.  Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis.

Authors:  Akari Suzuki; Ryo Yamada; Xiaotian Chang; Shinya Tokuhiro; Tetsuji Sawada; Masakatsu Suzuki; Miyuki Nagasaki; Makiko Nakayama-Hamada; Reimi Kawaida; Mitsuru Ono; Masahiko Ohtsuki; Hidehiko Furukawa; Shinichi Yoshino; Masao Yukioka; Shigeto Tohma; Tsukasa Matsubara; Shigeyuki Wakitani; Ryota Teshima; Yuichi Nishioka; Akihiro Sekine; Aritoshi Iida; Atsushi Takahashi; Tatsuhiko Tsunoda; Yusuke Nakamura; Kazuhiko Yamamoto
Journal:  Nat Genet       Date:  2003-08       Impact factor: 38.330

10.  An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.

Authors:  Shinya Tokuhiro; Ryo Yamada; Xiaotian Chang; Akari Suzuki; Yuta Kochi; Tetsuji Sawada; Masakatsu Suzuki; Miyuki Nagasaki; Masahiko Ohtsuki; Mitsuru Ono; Hidehiko Furukawa; Masakazu Nagashima; Shinichi Yoshino; Akihiko Mabuchi; Akihiro Sekine; Susumu Saito; Atsushi Takahashi; Tatsuhiko Tsunoda; Yusuke Nakamura; Kazuhiko Yamamoto
Journal:  Nat Genet       Date:  2003-11-09       Impact factor: 38.330

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  4 in total

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Authors:  Lynae J Hanks; Krista Casazza; Ambika P Ashraf; Sasanka Ramanadham; Jamy Ard; Molly S Bray; T Mark Beasley; Jose R Fernandez
Journal:  J Bone Miner Metab       Date:  2013-04-02       Impact factor: 2.626

2.  Phylogeography of two moray eels indicates high dispersal throughout the indo-pacific.

Authors:  Joshua S Reece; Brian W Bowen; Kavita Joshi; Vadim Goz; Allan Larson
Journal:  J Hered       Date:  2010-04-07       Impact factor: 2.645

3.  ParaHaplo 2.0: a program package for haplotype-estimation and haplotype-based whole-genome association study using parallel computing.

Authors:  Kazuharu Misawa; Naoyuki Kamatani
Journal:  Source Code Biol Med       Date:  2010-06-04

4.  ParaHaplo: A program package for haplotype-based whole-genome association study using parallel computing.

Authors:  Kazuharu Misawa; Naoyuki Kamatani
Journal:  Source Code Biol Med       Date:  2009-10-21
  4 in total

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