Literature DB >> 7825595

Inherent intractability of the ascertainment problem for pedigree data: a general likelihood framework.

V J Vieland1, S E Hodge.   

Abstract

The problem of ascertainment in segregation analysis arises when families are selected for study through ascertainment of affected individuals. In this case, ascertainment must be corrected for in data analysis. However, methods for ascertainment correction are not available for many common sampling schemes, e.g., sequential sampling of extended pedigrees (except in the case of "single" selection). Concerns about whether ascertainment correction is even required for large pedigrees, about whether and how multiple probands in the same pedigree can be taken into account properly, and about how to apply sequential sampling strategies have occupied many investigators in recent years. We address these concerns by reconsidering a central issue, namely, how to handle pedigree structure (including size). We introduce a new distinction, between sampling in such a way that observed pedigree structure does not depend on which pedigree members are probands (proband-independent [PI] sampling) and sampling in such a way that observed pedigree structure does depend on who are the probands (proband-dependent [PD] sampling). This distinction corresponds roughly (but not exactly) to the distinction between fixed-structure and sequential sampling. We show that conditioning on observed pedigree structure in ascertained data sets obtained under PD sampling is not in general correct (with the exception of "single" selection), while PI sampling of pedigree structures larger than simple sibships is generally not possible. Yet, in practice one has little choice but to condition on observed pedigree structure. We conclude that the problem of genetic modeling in ascertained data sets is, in most situations, literally intractable. We recommend that future efforts focus on the development of robust approximate approaches to the problem.

Entities:  

Mesh:

Year:  1995        PMID: 7825595      PMCID: PMC1801326     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  10 in total

1.  Genetic tests under incomplete ascertainment.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1959-03       Impact factor: 11.025

2.  Assumptions for different ascertainment models in human genetics.

Authors:  J S Williams; J Stene
Journal:  Biometrics       Date:  1977-09       Impact factor: 2.571

3.  Conditioning on subsets of the data: applications to ascertainment and other genetic problems.

Authors:  S E Hodge
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

4.  A resolution of the ascertainment sampling problem. III. Pedigrees.

Authors:  N C Shute; W J Ewens
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

5.  A resolution of the ascertainment sampling problem. I. Theory.

Authors:  W J Ewens; N C Shute
Journal:  Theor Popul Biol       Date:  1986-12       Impact factor: 1.570

6.  Likelihoods in pedigree analysis under sequential sampling.

Authors:  E Thompson
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

7.  Sampling considerations in the gathering and analysis of pedigree data.

Authors:  R C Elston; E Sobel
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

8.  Ascertainment in the sequential sampling of pedigrees.

Authors:  C Cannings; E A Thompson
Journal:  Clin Genet       Date:  1977-10       Impact factor: 4.438

9.  A general model for the genetic analysis of pedigree data.

Authors:  R C Elston; J Stewart
Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

10.  Spinal dysraphia as an autosomal dominant defect in four families.

Authors:  R M Fineman; L B Jorde; R A Martin; S J Hasstedt; S D Wing; M L Walker
Journal:  Am J Med Genet       Date:  1982-08
  10 in total
  21 in total

1.  Ascertainment adjustment: where does it take us?

Authors:  P R Burton; L J Palmer; K Jacobs; K J Keen; J M Olson; R C Elston
Journal:  Am J Hum Genet       Date:  2000-11-14       Impact factor: 11.025

2.  Likelihood formulation of parent-of-origin effects on segregation analysis, including ascertainment.

Authors:  Fatemeh Haghighi; Susan E Hodge
Journal:  Am J Hum Genet       Date:  2001-11-30       Impact factor: 11.025

3.  Ascertainment-adjusted parameter estimates revisited.

Authors:  Michael P Epstein; Xihong Lin; Michael Boehnke
Journal:  Am J Hum Genet       Date:  2002-03-05       Impact factor: 11.025

4.  Computer simulation is an undervalued tool for genetic analysis: a historical view and presentation of SHIMSHON--a Web-based genetic simulation package.

Authors:  David A Greenberg
Journal:  Hum Hered       Date:  2011-12-23       Impact factor: 0.444

5.  A framework for structural equation models in general pedigrees.

Authors:  Nathan J Morris; Robert C Elston; Catherine M Stein
Journal:  Hum Hered       Date:  2011-01-06       Impact factor: 0.444

6.  PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history.

Authors:  F Alarcon; C Bourgain; M Gauthier-Villars; V Planté-Bordeneuve; D Stoppa-Lyonnet; C Bonaïti-Pellié
Journal:  Genet Epidemiol       Date:  2009-07       Impact factor: 2.135

7.  Changing the definition of "proband" in the new standardized nomenclature for pedigrees.

Authors:  M L Marazita
Journal:  J Genet Couns       Date:  1996-03       Impact factor: 2.537

8.  Classification of Missense Mutations of Disease Genes.

Authors:  Xi Zhou; Edwin S Iversen; Giovanni Parmigiani
Journal:  J Am Stat Assoc       Date:  2005       Impact factor: 5.033

9.  Affecteds-only linkage methods are not a panacea.

Authors:  D A Greenberg; S E Hodge; V J Vieland; M A Spence
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

10.  A pseudolikelihood approach to correcting for ascertainment bias in family studies.

Authors:  D Rabinowitz
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.