Document Detail


Comparison of ascertainment-bias correction schemes for pedigrees ascertained through multiple probands.
MedLine Citation:
PMID:  4023475     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Assessing the genetic causation of a disease, which is of prime importance in medical genetics, is usually done by analysing pedigree data. When gathering such data, it is often more practical to adopt a non-random sampling strategy. However, unless suitable corrections for non-random sampling are made at the time of data analysis, inferences may be grossly affected. For pedigree data ascertained through multiple probands, various correction schemes have been suggested, although the efficiencies of these schemes are unknown. This paper compares such schemes, using Monte Carlo simulation techniques, under a simple genetic model, for pedigrees of fixed sizes and structures and for probands of two types of relationship--parent-offspring, and a pair of siblings. It is found that gene frequencies are grossly overestimated and the penetrance value of heterozygotes slightly underestimated whether or not any correction for non-random sampling of pedigrees is made. Knowledge of the population value of the gene frequency improves the estimate of the penetrance parameter.
Authors:
P P Majumder
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Statistics in medicine     Volume:  4     ISSN:  0277-6715     ISO Abbreviation:  Stat Med     Publication Date:    1985 Apr-Jun
Date Detail:
Created Date:  1985-09-25     Completed Date:  1985-09-25     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8215016     Medline TA:  Stat Med     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  163-73     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Biometry*
Female
Gene Frequency
Genetics, Medical*
Humans
Male
Models, Genetic
Monte Carlo Method
Pedigree*
Grant Support
ID/Acronym/Agency:
AG 01028/AG/NIA NIH HHS; CA 19311/CA/NCI NIH HHS; K0400230//PHS HHS

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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