Evidence map›Paper›PMID 18304491›Full record

ArticleAmerican journal of human genetics2008

Robust score statistics for QTL linkage analysis.

Samsiddhi Bhattacharjee, Chia-Ling Kuo, Nandita Mukhopadhyay, Guy N Brock, Daniel E Weeks, Eleanor Feingold

Abstract read
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Article in American journal of human genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Heritability Estimation using Regression Models for Correlation.Journal of biometrics & biostatistics · 2011
    Article
  3. Article
  4. Article
  5. Article
  6. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Samsiddhi BhattacharjeeDepartment of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Chia-Ling Kuo
Nandita Mukhopadhyay
Guy N Brock
Daniel E Weeks
Eleanor Feingold

Funding

Mega2: Manipulation Environment for Genetic AnalysesR01GM076667 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WEEKS, DANIEL E · 2006 to 2018
$3.2M
India-US Research Training Program in GeneticsD43TW006180 · FIC · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WEEKS, DANIEL E · 2002 to 2006
$1.8M
Human QTL Mapping With Selected SamplesR01HG002374 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FEINGOLD, ELEANOR · 2001 to 2007
$846k
DISCOVERING GENES FOR MENTAL HEALTHT32MH020053 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WEEKS, DANIEL E · 2000 to 2004
$451k
FIC NIH HHS D43 TW006180NHGRI NIH HHS R01 HG002374NIGMS NIH HHS R01 GM076667NIMH NIH HHS T32 MH020053
6 · The paper itself

Abstract

The traditional variance components approach for quantitative trait locus (QTL) linkage analysis is sensitive to violations of normality and fails for selected sampling schemes. Recently, a number of new methods have been developed for QTL mapping in humans. Most of the new methods are based on score statistics or regression-based statistics and are expected to be relatively robust to non-normality of the trait distribution and also to selected sampling, at least in terms of type I error. Whereas the theoretical development of these statistics is more or less complete, some practical issues concerning their implementation still need to be addressed. Here we study some of these issues such as the choice of denominator variance estimates, weighting of pedigrees, effect of parameter misspecification, effect of non-normality of the trait distribution, and effect of incorporating dominance. We present a comprehensive discussion of the theoretical properties of various denominator variance estimates and of the weighting issue and then perform simulation studies for nuclear families to compare the methods in terms of power and robustness. Based on our analytical and simulation results, we provide general guidelines regarding the choice of appropriate QTL mapping statistics in practical situations.

Indexed as

Computer SimulationGenetic LinkageModels, GeneticQuantitative Trait LociChromosome MappingHumansPedigree

Identifiers

PMID18304491
PMCPMC2427220

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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.