Literature DB >> 3177380

A resolution of the ascertainment sampling problem. II. Generalizations and numerical results.

N C Shute1, W J Ewens.   

Abstract

The ascertainment problem arises when families are sampled by a nonrandom process and some assumption about this sampling process must be made in order to estimate genetic parameters. Under classical ascertainment assumptions, estimation of genetic parameters cannot be separated from estimation of the parameters of the ascertainment process, so that any misspecification of the ascertainment process causes biases in estimation of the genetic parameters. Ewens and Shute proposed a resolution to this problem, involving conditioning the likelihood of the sample on the part of the data which is "relevant to ascertainment." The usefulness of this approach can only be assessed by examining the properties (in particular, bias and standard error) of the estimates which arise by using it for a wide range of parameter values and family size distributions and then comparing these biases and standard errors with those arising under classical ascertainment procedures. These comparisons are carried out in the present paper, and we also compare the proposed method with procedures which condition on, or ignore, parts of the data.

Mesh:

Year:  1988        PMID: 3177380      PMCID: PMC1715491     

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


  7 in total

1.  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

2.  The effect of proband designation on segregation analysis.

Authors:  D A Greenberg
Journal:  Am J Hum Genet       Date:  1986-09       Impact factor: 11.025

3.  Ascertainment considerations in the analysis of affected sib shared haplotype data.

Authors:  W J Ewens; N C Shute; N J Cox; R A Price; R S Spielman
Journal:  Genet Epidemiol Suppl       Date:  1986

4.  Segregation analysis incorporating linkage markers. I. Single-locus models with an application to type I diabetes.

Authors:  N Risch
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

5.  Maximum likelihood estimation of genetic parameters of HLA-linked diseases using data from families of various sizes.

Authors:  W J Ewens; C P Clarke
Journal:  Am J Hum Genet       Date:  1984-07       Impact factor: 11.025

6.  Complex segregation analysis with pointers.

Authors:  J M Lalouel; N E Morton
Journal:  Hum Hered       Date:  1981       Impact factor: 0.444

7.  The estimation of phenotype distributions from pedigree data.

Authors:  R M Winter
Journal:  Am J Med Genet       Date:  1980
  7 in total
  5 in total

1.  A cooperative binomial ascertainment model.

Authors:  E Kh Ginsburg; T I Axenovich
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

2.  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

3.  Familial recurrence risk with varying amount of family history.

Authors:  Daniel J Schaid; Shannon K McDonnell; Stephen N Thibodeau
Journal:  Genet Epidemiol       Date:  2019-02-11       Impact factor: 2.135

4.  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

5.  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 in total

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