Evidence map›Paper›PMID 22740194›Full record

ArticleGenetic epidemiology2012

Computationally efficient multipoint linkage analysis on extended pedigrees for trait models with two contributing major Loci.

Ming Su, Elizabeth A Thompson

Abstract read
In one paragraph

Article in Genetic epidemiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Efficient identification of equivalences in dynamic graphs and pedigree structures.Journal of computational biology : a journal of computational molecular cell biology · 2013
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Ming SuDepartment of Electrical Engineering, University of Washington, Seattle, Washington 98195-4322, USA.
Elizabeth A Thompson

Funding

Statistical Methods for X-Chromosome Genetic DataP01GM099568 · NIGMS · UNIVERSITY OF WASHINGTON · PI WEIR, BRUCE S. · 2012 to 2016
$7.3M
Methods for the Genetic Epidemiology of Complex TraitsR37GM046255 · NIGMS · UNIVERSITY OF WASHINGTON · PI THOMPSON, ELIZABETH ALISON · 2008 to 2017
$4.2M
THE GENETIC EPIDEMIOLOGY OF COMPLEX TRAITSR01GM046255 · NIGMS · UNIVERSITY OF WASHINGTON · PI THOMPSON, ELIZABETH ALISON · 1991 to 2007
$2.7M
Efficient software and algorithms for analyzing markers data on general pedigreeR01HG004175 · NHGRI · UNIVERSITY OF CALIFORNIA-IRVINE · PI DECHTER, RINA · 2007 to 2010
$1.2M
NHGRI NIH HHS HG004175NHGRI NIH HHS R01 HG004175NIGMS NIH HHS GM046255NIGMS NIH HHS P01 GM099568NIGMS NIH HHS R01 GM046255NIGMS NIH HHS R37 GM046255
6 · The paper itself

Abstract

We have developed a computationally efficient method for multipoint linkage analysis on extended pedigrees for trait models having a two-locus quantitative trait loci (QTL) effect. The method has been implemented in the program, hg_lod, which uses the Markov chain Monte Carlo (MCMC) method to sample realizations of descent patterns conditional on marker data, then calculates the trait likelihood for each realization by efficient exact computation. Given its computational efficiency, hg_lod can handle data on large pedigrees with a lot of unobserved individuals, and can compute accurate estimates of logarithm of odds (lod) scores at a much larger number of hypothesized locations than can any existing method. We have compared hg_lod to lm_twoqtl, the first publically available linkage program for trait models with two major loci, using simulated data. Results show that our method is orders of magnitude faster while the accuracy of QTL localization is retained. The efficiency of our method also facilitates analyses with multiple trait models, for example, sensitivity analysis. Additionally, since the MCMC sampling conditions only on the marker data, there is no need to resample the descent patterns to compute likelihoods under alternative trait models. This achieves additional computational efficiency.

Indexed as

Genetic LinkageModels, GeneticQuantitative Trait LociComputer SimulationHumansLod ScoreMarkov ChainsMonte Carlo MethodPedigreePolymorphism, Single NucleotideSample Size

Identifiers

PMID22740194
PMCPMC3868922

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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.