Volume 6, Issue 1 pp. 253-258
Original Article
Full Access

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

Dr. Maria Martinez

Corresponding Author

Dr. Maria Martinez

INSERM U. 155, Chateau de Longchamp, Bois de Boulogne, Paris

Clinical Neurogenesis Branch, NIMH, Building 10, Room 3N218, 9000 Rockville Pike, Bethesda, MD 20892Search for more papers by this author
Myriam Khlat

Myriam Khlat

Laboratoire de Biometrie, Université Lyon I, Villeurbanne, France

Search for more papers by this author
Marion Leboyer

Marion Leboyer

INSERM U. 155, Chateau de Longchamp, Bois de Boulogne, Paris

Search for more papers by this author
Françoise Clerget-Darpoux

Françoise Clerget-Darpoux

INSERM U. 155, Chateau de Longchamp, Bois de Boulogne, Paris

Search for more papers by this author
First published: 1989
Citations: 35

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.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.