Evidence map›Paper›PMID 22697240›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2012

Efficient simulation and likelihood methods for non-neutral multi-allele models.

Paul Joyce, Alan Genz, Erkan Ozge Buzbas

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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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

3 authors.

Paul JoyceDepartment of Mathematics and Initiative for Bioinformatics and Evolutionary Studies, University of Idaho, Moscow, ID, USA.
Alan Genz
Erkan Ozge Buzbas

Funding

UNDERGRADUATE COLLEGE OUTREACH PROGRAMP20RR016454 · NCRR · UNIVERSITY OF IDAHO · PI CHASE, JENNIFER R · 2001 to 2011
$35.3M
The Evolution of Protein FlexibilityP20RR016448 · NCRR · UNIVERSITY OF IDAHO · PI ROBISON, BARRIE D · 2002 to 2011
$19.3M
Patterns of Adaptive EvolutionR01GM076040 · NIGMS · UNIVERSITY OF IDAHO · PI MILLER, CRAIG R, WICHMAN, HOLLY A · 2006 to 2021
$3.6M
Population-Genetic Studies for Association MappingR01GM081441 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSENBERG, NOAH · 2007 to 2011
$1.7M
NCRR NIH HHS 1P20RR016448-01NCRR NIH HHS P20 RR016454NIGMS NIH HHS R01 GM076040NIGMS NIH HHS R01 GM081441
6 · The paper itself

Abstract

Throughout the 1980s, Simon Tavaré made numerous significant contributions to population genetics theory. As genetic data, in particular DNA sequence, became more readily available, a need to connect population-genetic models to data became the central issue. The seminal work of Griffiths and Tavaré (1994a , 1994b , 1994c) was among the first to develop a likelihood method to estimate the population-genetic parameters using full DNA sequences. Now, we are in the genomics era where methods need to scale-up to handle massive data sets, and Tavaré has led the way to new approaches. However, performing statistical inference under non-neutral models has proved elusive. In tribute to Simon Tavaré, we present an article in spirit of his work that provides a computationally tractable method for simulating and analyzing data under a class of non-neutral population-genetic models. Computational methods for approximating likelihood functions and generating samples under a class of allele-frequency based non-neutral parent-independent mutation models were proposed by Donnelly, Nordborg, and Joyce (DNJ) (Donnelly et al., 2001). DNJ (2001) simulated samples of allele frequencies from non-neutral models using neutral models as auxiliary distribution in a rejection algorithm. However, patterns of allele frequencies produced by neutral models are dissimilar to patterns of allele frequencies produced by non-neutral models, making the rejection method inefficient. For example, in some cases the methods in DNJ (2001) require 10(9) rejections before a sample from the non-neutral model is accepted. Our method simulates samples directly from the distribution of non-neutral models, making simulation methods a practical tool to study the behavior of the likelihood and to perform inference on the strength of selection.

Indexed as

AlgorithmsModels, GeneticAllelesComputer SimulationGene FrequencyGenetics, PopulationHumansLikelihood FunctionsMutationSelection, GeneticSequence Analysis, DNA

Identifiers

PMID22697240
PMCPMC3375650

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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.