Evidence map›Paper›PMID 26341659›Full record

ArticleGenetics2015

Inferring Bottlenecks from Genome-Wide Samples of Short Sequence Blocks.

Lynsey Bunnefeld, Laurent A F Frantz, Konrad Lohse

Abstract read
In one paragraph

Article in Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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  14. Whole-genome data reveal the complex history of a diverse ecological community.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. Survival and divergence in a small group: The extraordinary genomic history of the endangered Apennine brown bear stragglers.Proceedings of the National Academy of Sciences of the United States of America · 2017
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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.

Lynsey BunnefeldInstitute of Evolutionary Biology, University of Edinburgh, Edinburgh EH9 3FL, United Kingdom lynsey.mcinnes@ed.ac.uk.
Laurent A F FrantzAnimal Breeding and Genomics Centre, Wageningen University, Wageningen 6708 PB, The Netherlands.
Konrad LohseInstitute of Evolutionary Biology, University of Edinburgh, Edinburgh EH9 3FL, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The advent of the genomic era has necessitated the development of methods capable of analyzing large volumes of genomic data efficiently. Being able to reliably identify bottlenecks--extreme population size changes of short duration--not only is interesting in the context of speciation and extinction but also matters (as a null model) when inferring selection. Bottlenecks can be detected in polymorphism data via their distorting effect on the shape of the underlying genealogy. Here, we use the generating function of genealogies to derive the probability of mutational configurations in short sequence blocks under a simple bottleneck model. Given a large number of nonrecombining blocks, we can compute maximum-likelihood estimates of the time and strength of the bottleneck. Our method relies on a simple summary of the joint distribution of polymorphic sites. We extend the site frequency spectrum by counting mutations in frequency classes in short sequence blocks. Using linkage information over short distances in this way gives greater power to detect bottlenecks than the site frequency spectrum and potentially opens up a wide range of demographic histories to blockwise inference. Finally, we apply our method to genomic data from a species of pig (Sus cebifrons) endemic to islands in the center and west of the Philippines to estimate whether a bottleneck occurred upon island colonization and compare our scheme to Li and Durbin's pairwise sequentially Markovian coalescent (PSMC) both for the pig data and using simulations.

Indexed as

Models, GeneticPopulation DynamicsAnimalsBase SequenceGenomeIslandsMutationPedigreePhilippinesSwinedemographic inferencegenerating functionmaximum likelihoodpopulation bottleneckSus cebifrons

Identifiers

PMID26341659
PMCPMC4649642

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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.