Evidence map›Paper›PMID 24831947›Full record

ArticlePLoS genetics2014

Genome-wide inference of ancestral recombination graphs.

Matthew D Rasmussen, Melissa J Hubisz, Ilan Gronau, Adam Siepel

Abstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 212 papers.

0numbers the graph read from it
0cells of the map it votes in
212citing 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

212 citing papers in PubMed.

  1. Review
  2. Genetics and genomics of hybridization.Nature reviews. Genetics · 2026
    Review
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  5. Review
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  17. Review
  18. Polarising SNPs Without Outgroup.Molecular ecology resources · 2026
    Article
  19. Article
  20. Article

152 more citing papers are in PubMed but not listed here.

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

4 authors.

Matthew D RasmussenDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America.
Melissa J HubiszDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America.
Ilan GronauDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America.
Adam SiepelDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambs, United Kingdom.

Funding

Computational methods for human genomic data integration: demography, selection,R01GM102192 · NIGMS · CORNELL UNIVERSITY · PI SIEPEL, ADAM CHARLES · 2013 to 2017
$1.7M
NIGMS NIH HHS GM102192NIGMS NIH HHS R01 GM102192
6 · The paper itself

Abstract

The complex correlation structure of a collection of orthologous DNA sequences is uniquely captured by the "ancestral recombination graph" (ARG), a complete record of coalescence and recombination events in the history of the sample. However, existing methods for ARG inference are computationally intensive, highly approximate, or limited to small numbers of sequences, and, as a consequence, explicit ARG inference is rarely used in applied population genomics. Here, we introduce a new algorithm for ARG inference that is efficient enough to apply to dozens of complete mammalian genomes. The key idea of our approach is to sample an ARG of [Formula: see text] chromosomes conditional on an ARG of [Formula: see text] chromosomes, an operation we call "threading." Using techniques based on hidden Markov models, we can perform this threading operation exactly, up to the assumptions of the sequentially Markov coalescent and a discretization of time. An extension allows for threading of subtrees instead of individual sequences. Repeated application of these threading operations results in highly efficient Markov chain Monte Carlo samplers for ARGs. We have implemented these methods in a computer program called ARGweaver. Experiments with simulated data indicate that ARGweaver converges rapidly to the posterior distribution over ARGs and is effective in recovering various features of the ARG for dozens of sequences generated under realistic parameters for human populations. In applications of ARGweaver to 54 human genome sequences from Complete Genomics, we find clear signatures of natural selection, including regions of unusually ancient ancestry associated with balancing selection and reductions in allele age in sites under directional selection. The patterns we observe near protein-coding genes are consistent with a primary influence from background selection rather than hitchhiking, although we cannot rule out a contribution from recurrent selective sweeps.

Indexed as

Evolution, MolecularGenome, HumanRecombination, GeneticAlgorithmsComputer SimulationHumansMarkov ChainsModels, GeneticMonte Carlo MethodSelection, Genetic

Identifiers

PMID24831947
PMCPMC4022496

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Registered trials

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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.