Evidence map›Paper›PMID 18466490›Full record

ArticleBMC proceedings2007

Two-step intermediate fine mapping with likelihood ratio test statistics: applications to Problems 2 and 3 data of GAW15.

Ritwik Sinha, Yuqun Luo

Abstract read
In one paragraph

Article in BMC proceedings, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Bayesian intervals for linkage locations.Genetic epidemiology · 2009
    Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Ritwik SinhaDivision of Genetic and Molecular Epidemiology, Department of Epidemiology and Biostatistics, Case Western Reserve University School of Medicine, Wolstein Research Building, 10900 Euclid Avenue, Cleveland, Ohio 44106, USA. rsinha@darwin.cwru.edu
Yuqun Luo

Funding

X-LINKED EXTENSION OF THE REVISED HASEMAN-ELSTON ALGORITHM FOR LINKAGE ANALYSISP41RR003655 · NCRR · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1987 to 2011
$11.5M
NCRR NIH HHS P41 RR003655
6 · The paper itself

Abstract

Construction of precise confidence sets of disease gene locations after initial identification of linked regions can improve the efficiency of the ensuing fine mapping effort. We took the confidence set inference, a framework proposed and implemented using the Mean test statistic (CSI-Mean) and improved the efficiency substantially by using a likelihood ratio test statistic (CSI-MLS). The CSI framework requires knowledge of some disease-model-related parameters. In the absence of prior knowledge of these parameters, a two-step procedure may be employed: 1) the parameters are estimated using a coarse map of markers; 2) CSI-Mean or CSI-MLS are applied to construct the confidence sets of the disease gene locations using a finer map of markers, assuming the estimates from Step 1 for the required parameters. In this article we show that the advantages of CSI-MLS over CSI-Mean, previously demonstrated when the required parameters are known, are preserved in this two-step procedure, using both the simulated and real data contributed to Problems 2 and 3 of Genetic Analysis Workshop 15. In addition, our result suggests that microsatellite data, when available, should be used in Step 1. Also explored in detail is the effect of the absence of parental genotypes on the performance of CSI-MLS.

Identifiers

PMID18466490
PMCPMC2367514

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.