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Rapid adaptation with gene flow via a reservoir of chromosomal inversion variation?

https://doi.org/10.1101/150771
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-0-387-21822-9openalex-snapshot
Mathematical Population Genetics : I. Theoretical Introduction
inferredcites →https://doi.org/10.1016/0040-5809(74)90022-7openalex-snapshot
Stable linkage disequilibrium without epistasis in subdivided populations
inferredcites →https://doi.org/10.1016/j.tree.2007.09.008openalex-snapshot
Adaptation from standing genetic variation
inferredcites →https://doi.org/10.1016/j.tree.2008.10.011openalex-snapshot
Ecological explanations for (incomplete) speciation
inferredcites →https://doi.org/10.1016/s0169-5347(01)02187-5openalex-snapshot
Chromosomal rearrangements and speciation
inferredcites →https://doi.org/10.1017/cbo9780511623486openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1017/s0305004100015644openalex-snapshot
A Mathematical Theory of Natural and Artificial Selection, Part V: Selection and Mutation
inferredcites →https://doi.org/10.1038/376762a0openalex-snapshot
Genetic mapping of floral traits associated with reproductive isolation in monkeyflowers (Mimulus)
inferredcites →https://doi.org/10.1038/nature10341openalex-snapshot
Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry
inferredcites →https://doi.org/10.1038/scientificamerican1179-98openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1073/pnas.0401720101openalex-snapshot
Pattern of polymorphism after strong artificial selection in a domestication event
inferredcites →https://doi.org/10.1073/pnas.0709806105openalex-snapshot
A test of the chromosomal theory of ecotypic speciation in Anopheles gambiae
inferredcites →https://doi.org/10.1073/pnas.0912748107openalex-snapshot
Phenotypic plasticity facilitates recurrent rapid adaptation to introduced predators
inferredcites →https://doi.org/10.1073/pnas.1010836107openalex-snapshot
Scaling expectations for the time to establishment of complex adaptations
inferredcites →https://doi.org/10.1073/pnas.1106085108openalex-snapshot
Speciation with gene flow on Lord Howe Island
inferredcites →https://doi.org/10.1073/pnas.1434337100openalex-snapshot
Semipermeable species boundaries between Anopheles gambiae and Anopheles arabiensis : Evidence from multilocus DNA sequence variation
inferredcites →https://doi.org/10.1073/pnas.1730757100openalex-snapshot
Allopatric genetic origins for sympatric host-plant shifts and race formation in Rhagoletis
inferredcites →https://doi.org/10.1073/pnas.221274498openalex-snapshot
Chromosomal inversions and the reproductive isolation of species
inferredcites →https://doi.org/10.1073/pnas.91.15.6885openalex-snapshot
Molecular phylogeny of the Anopheles gambiae complex suggests genetic introgression between principal malaria vectors.
inferredcites →https://doi.org/10.1086/589460openalex-snapshot
Population Extinction and the Genetics of Adaptation
inferredcites →https://doi.org/10.1093/genetics/146.2.723openalex-snapshot
The Probability of Fixation in Populations of Changing Size
inferredcites →https://doi.org/10.1093/genetics/157.2.875openalex-snapshot
Haldane's Sieve and Adaptation From the Standing Genetic Variation
inferredcites →https://doi.org/10.1093/genetics/16.2.97openalex-snapshot
EVOLUTION IN MENDELIAN POPULATIONS
inferredcites →https://doi.org/10.1093/genetics/163.3.939openalex-snapshot
Evidence for Inversion Polymorphism Related to Sympatric Host Race Formation in the Apple Maggot Fly,Rhagoletis pomonella
inferredcites →https://doi.org/10.1093/genetics/57.4.741openalex-snapshot
FREQUENCY CHANGES OF NEW INVERSIONS IN POPULATIONS UNDER MUTATION-SELECTION EQUILIBRIA
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00591.xopenalex-snapshot
EVOLUTIONARY PACE OF CHROMOSOMAL POLYMORPHISM IN COLONIZING POPULATIONS OF DROSOPHILA SUBOBSCURA: AN EVOLUTIONARY TIME SERIES
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01537.xopenalex-snapshot
ACCUMULATING POSTZYGOTIC ISOLATION GENES IN PARAPATRY: A NEW TWIST ON CHROMOSOMAL SPECIATION
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03946.xopenalex-snapshot
Divergent selection and heterogeneous genomic divergence
inferredcites →https://doi.org/10.1111/j.1558-5646.1960.tb03113.xopenalex-snapshot
THE EVOLUTIONARY DYNAMICS OF COMPLEX POLYMORPHISMS,,
inferredcites →https://doi.org/10.1111/j.1558-5646.1998.tb01823.xopenalex-snapshot
THE POPULATION GENETICS OF ADAPTATION: THE DISTRIBUTION OF FACTORS FIXED DURING ADAPTIVE EVOLUTION
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00835.xopenalex-snapshot
CLINAL PATTERNS OF CHROMOSOMAL INVERSION POLYMORPHISMS INDROSOPHILA SUBOBSCURAARE PARTLY ASSOCIATED WITH THERMAL PREFERENCES AND HEAT STRESS RESISTANCE
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01269.xopenalex-snapshot
THE GENETIC ARCHITECTURE OF ADAPTATION UNDER MIGRATION-SELECTION BALANCE
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01321.xopenalex-snapshot
ADAPTIVE CHROMOSOMAL DIVERGENCE DRIVEN BY MIXED GEOGRAPHIC MODE OF EVOLUTION
inferredcites →https://doi.org/10.1126/science.1077769openalex-snapshot
A Polytene Chromosome Analysis of the Anopheles gambiae Species Complex
inferredcites →https://doi.org/10.1126/science.1107239openalex-snapshot
Widespread Parallel Evolution in Sticklebacks by Repeated Fixation of Ectodysplasin Alleles
inferredcites →https://doi.org/10.1186/1471-2148-8-309openalex-snapshot
Chromosomal plasticity and evolutionary potential in the malaria vector Anopheles gambiae sensu stricto: insights from three decades of rare paracentric inversions
inferredcites →https://doi.org/10.1214/aoms/1177706791openalex-snapshot
Some Problems of Stochastic Processes in Genetics
inferredcites →https://doi.org/10.1371/journal.pbio.1000500openalex-snapshot
A Widespread Chromosomal Inversion Polymorphism Contributes to a Major Life-History Transition, Local Adaptation, and Reproductive Isolation
inferredcites →https://doi.org/10.1371/journal.pbio.1000501openalex-snapshot
How and Why Chromosome Inversions Evolve
inferredcites →https://doi.org/10.1371/journal.pgen.0030217openalex-snapshot
Localization of Candidate Regions Maintaining a Common Polymorphic Inversion (2La) in Anopheles gambiae
inferredcites →https://doi.org/10.1371/journal.pgen.1000924openalex-snapshot
Evidence that Adaptation in Drosophila Is Not Limited by Mutation at Single Sites
inferredcites →https://doi.org/10.1534/genetics.104.036947openalex-snapshot
Soft Sweeps
inferredcites →https://doi.org/10.1534/genetics.105.047985openalex-snapshot
Chromosome Inversions, Local Adaptation and Speciation
inferredcites →https://doi.org/10.1534/genetics.108.097857openalex-snapshot
Recombination Load in a Chromosomal Inversion Polymorphism of Drosophila subobscura
inferredcites →https://doi.org/10.1554/02-577openalex-snapshot
EVOLUTIONARY PACE OF CHROMOSOMAL POLYMORPHISM IN COLONIZING POPULATIONS OF DROSOPHILA SUBOBSCURA: AN EVOLUTIONARY TIME SERIES
inferredcites →https://doi.org/10.1554/05-273.1openalex-snapshot
THE SIGNATURE OF POSITIVE SELECTION ON STANDING GENETIC VARIATION
inferredcites →https://doi.org/10.2307/2528314openalex-snapshot
Survival Probabilities of New Inversions in Large Populations
inferredcites →https://doi.org/10.5962/bhl.title.27468openalex-snapshot
The genetical theory of natural selection

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inferred← citeshttps://doi.org/10.1007/s12298-019-00736-7openalex-snapshot
Chloroplast genome of an extremely endangered conifer Thuja sutchuenensis Franch.: gene organization, comparative and phylogenetic analysis
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