Evidence map›Paper›PMID 28961717›Full record

ArticleMolecular biology and evolution2017

Quantifying Selection with Pool-Seq Time Series Data.

Thomas Taus, Andreas Futschik, Christian Schlötterer

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
–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

63 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Direct estimation of genotype fitness from time series.bioRxiv : the preprint server for biology · 2026
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  8. Beyond Fixation: Persistent Genetic Variation Under Intense Selection.bioRxiv : the preprint server for biology · 2026
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3 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

3 authors.

Thomas TausInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria.
Andreas FutschikDepartment of Applied Statistics, Johannes Kepler Universität Linz, Linz, Austria.
Christian SchlöttererInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria.

Funding

Austrian Science Fund FWF W 1225
6 · The paper itself

Abstract

Allele frequency time series data constitute a powerful resource for unraveling mechanisms of adaptation, because the temporal dimension captures important information about evolutionary forces. In particular, Evolve and Resequence (E&R), the whole-genome sequencing of replicated experimentally evolving populations, is becoming increasingly popular. Based on computer simulations several studies proposed experimental parameters to optimize the identification of the selection targets. No such recommendations are available for the underlying parameters selection strength and dominance. Here, we introduce a highly accurate method to estimate selection parameters from replicated time series data, which is fast enough to be applied on a genome scale. Using this new method, we evaluate how experimental parameters can be optimized to obtain the most reliable estimates for selection parameters. We show that the effective population size (Ne) and the number of replicates have the largest impact. Because the number of time points and sequencing coverage had only a minor effect, we suggest that time series analysis is feasible without major increase in sequencing costs. We anticipate that time series analysis will become routine in E&R studies.

Indexed as

Adaptation, BiologicalAdaptation, PhysiologicalAllelesBiological EvolutionComputer SimulationEvolution, MolecularGene FrequencyGenomeModels, GeneticPolymorphism, Single NucleotideSelection, GeneticSequence Analysis, DNAWhole Genome Sequencingevolve and resequenceselectionsoftwaretime series

Identifiers

PMID28961717
PMCPMC5850601

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Registered trials

None linked

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.