Evidence map›Paper›PMID 22257666›Full record

ArticleBioinformatics (Oxford, England)2012

Exact coalescent simulation of new haplotype data from existing reference haplotypes.

Chul Joo Kang, Paul Marjoram

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2012. 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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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

1 citing paper in PubMed.

  1. Article
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.

Chul Joo KangDepartment of Preventive Medicine, University of Southern California, Los Angeles, CA 90089, USA. chulkang@usc.edu
Paul Marjoram

Funding

Statistical Methods for Relating Sequence Data to PhenotypeR01MH084678 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MARJORAM, PAUL · 2008 to 2010
$1.6M
NIMH NIH HHS MH084678
6 · The paper itself

Abstract

motivationWe introduce a coalescent-based method (RECOAL) for the simulation of new haplotype data from a reference population of haplotypes. A coalescent genealogy for the reference haplotype data is sampled from the appropriate posterior probability distribution, then a coalescent genealogy is simulated which extends the sampled genealogy to include new haplotype data. The new haplotype data will, therefore, contain both some of the existing polymorphic sites and new polymorphisms added based on the structure of the simulated coalescent genealogy. This allows exact coalescent simulation of new haplotype data, compared with other methods which are more approximate in nature.

resultsWe demonstrate the performance of our method using a variety of data simulated under a coalescent model, before applying it to data from the 1000 Genomes project.

Indexed as

Genome, HumanModels, GeneticAlgorithmsComputer SimulationGenome-Wide Association StudyHaplotypesHumansPopulation GroupsProbability

Identifiers

PMID22257666
PMCPMC3307111

What OpenQuestion holds

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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.