Ascertainment-adjusted parameter estimates revisited.

نویسندگان

  • Michael P Epstein
  • Xihong Lin
  • Michael Boehnke
چکیده

Ascertainment-adjusted parameter estimates from a genetic analysis are typically assumed to reflect the parameter values in the original population from which the ascertained data were collected. Burton et al. (2000) recently showed that, given unmodeled parameter heterogeneity, the standard ascertainment adjustment leads to biased parameter estimates of the population-based values. This finding has important implications in complex genetic studies, because of the potential existence of unmodeled genetic parameter heterogeneity. The authors further stated the important point that, given unmodeled heterogeneity, the ascertainment-adjusted parameter estimates reflect the true parameter values in the ascertained subpopulation. They illustrated these statements with two examples. By revisiting these examples, we demonstrate that if the ascertainment scheme and the nature of the data can be correctly modeled, then an ascertainment-adjusted analysis returns population-based parameter estimates. We further demonstrate that if the ascertainment scheme and data cannot be modeled properly, then the resulting ascertainment-adjusted analysis produces parameter estimates that generally do not reflect the true values in either the original population or the ascertained subpopulation.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Comment on "Ascertainment adjustment in complex diseases".

Glidden and Liang [2002] have raised important issues regarding ascertainment adjustment in the framework of variance-components modeling for complex genetic traits. While the structure of the authors’ logistic variance-component model is simple, ascertainment issues arising with this model are likely analogous to ascertainment issues in more complex variance-component models commonly used for ...

متن کامل

Estimating the prevalence of polymyositis and dermatomyositis from administrative data: age, sex and regional differences.

OBJECTIVE To estimate the prevalence of polymyositis and dermatomyositis using population-based administrative data, the sensitivity of case ascertainment approaches and patient demographics and these parameters. METHODS Cases were ascertained from Quebec physician billing and hospitalisation databases (approximately 7.5 million beneficiaries). Three different case definition algorithms were ...

متن کامل

Overcoming the winner's curse: estimating penetrance parameters from case-control data.

Genomewide association studies are now a widely used approach in the search for loci that affect complex traits. After detection of significant association, estimates of penetrance and allele-frequency parameters for the associated variant indicate the importance of that variant and facilitate the planning of replication studies. However, when these estimates are based on the original data used...

متن کامل

The Effect of Estimation Error on Risk-adjusted Bernoulli GEWMA Control Chart in Multistage Healthcare Processes

Background and objectives: Risk-adjusted Bernoulli control chart is one of the main tools for monitoring multistage healthcare processes to achieve higher performance and effectiveness in healthcare settings. Using parameter estimates can lead to significantly deteriorate chart performance. However, so far, the effect of estimation error on this chart in which healthcare ...

متن کامل

Correcting coalescent analyses for panel-based SNP ascertainment.

Single-nucleotide polymorphism (SNP) data are routinely obtained by sequencing a region of interest in a small panel, constructing a chip with probes specific to sites found to vary in the panel, and using the chip to assay subsequent samples. The size of the chip is often reduced by removing low-frequency alleles from the set of SNPs. Using coalescent estimation of the scaled population size p...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • American journal of human genetics

دوره 70 4  شماره 

صفحات  -

تاریخ انتشار 2002