Literature DB >> 2731714

Performance of linkage analysis under misclassification error when the genetic model is unknown.

M Martinez1, M Khlat, M Leboyer, F Clerget-Darpoux.   

Abstract

Linkage analysis of complex diseases raises a number of important methodological problems. One of them concerns the clinical classification of disease phenotypes. In this study, we investigate the effects of false positive misclassification on the estimation of the recombination fraction and on the power and the robustness of tests for linkage. These effects are investigated 1) when the genetic model of the trait locus is known; and 2) when it is unknown, by maximizing the likelihood of the marker configuration given the disease status in the family. Results show that linkage analysis of misclassified data leads to an overestimation of the recombination fraction and a loss of power of the linkage test. The results are quite similar in both situations. However, the linkage test itself is robust to this kind of misclassification error.

Mesh:

Substances:

Year:  1989        PMID: 2731714     DOI: 10.1002/gepi.1370060144

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  6 in total

1.  Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes.

Authors:  H H Göring; J D Terwilliger
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

Review 2.  Current perspectives on the genetics of unipolar depression.

Authors:  S O Moldin; T Reich; J P Rice
Journal:  Behav Genet       Date:  1991-05       Impact factor: 2.805

3.  Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees.

Authors:  Alejandro A Schäffer; Mathieu Lemire; Jürg Ott; G Mark Lathrop; Daniel E Weeks
Journal:  Hum Hered       Date:  2011-07-06       Impact factor: 0.444

4.  Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus.

Authors:  Wei-Qi Wei; Cynthia L Leibson; Jeanine E Ransom; Abel N Kho; Pedro J Caraballo; High Seng Chai; Barbara P Yawn; Jennifer A Pacheco; Christopher G Chute
Journal:  J Am Med Inform Assoc       Date:  2012-01-16       Impact factor: 4.497

5.  The absence of longitudinal data limits the accuracy of high-throughput clinical phenotyping for identifying type 2 diabetes mellitus subjects.

Authors:  Wei-Qi Wei; Cynthia L Leibson; Jeanine E Ransom; Abel N Kho; Christopher G Chute
Journal:  Int J Med Inform       Date:  2012-07-02       Impact factor: 4.046

6.  The reliability of the SADS-LA in a family study setting.

Authors:  M Leboyer; W Maier; M Teherani; D Lichtermann; T D'Amato; P Franke; J P Lépine; J Minges; P McGuffin
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.