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Nonneutral Admixture of Immigrant Genotypes in African Drosophila melanogaster Populations from Zimbabwe

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

inferreduses_data →https://doi.org/10.5281/zenodo.10723540zenodo-depositor-declared
inferredcites →https://doi.org/10.1007/978-1-4615-2383-3_4openalex-snapshot
Selection, Recombination, and DNA Polymorphism in Drosophila
inferredcites →https://doi.org/10.1007/978-3-0348-7582-0_10openalex-snapshot
The Use of Imperfect Microsatellites for DNA Fingerprinting and Population Genetics
inferredcites →https://doi.org/10.1007/978-94-010-0585-2_31openalex-snapshot
Adaptive divergence and the evolution of reproductive isolation in the wild: An empirical demonstration using introduced sockeye salmon
inferredcites →https://doi.org/10.1007/s004380100531openalex-snapshot
DDT resistance in Drosophila correlates with Cyp6g1 over-expression and confers cross-resistance to the neonicotinoid imidacloprid
inferredcites →https://doi.org/10.1016/0168-9525(88)90098-4openalex-snapshot
Genetic variation of Drosophila melanogaster natural populations
inferredcites →https://doi.org/10.1016/s0169-5347(01)02198-xopenalex-snapshot
Ecology and the origin of species
inferredcites →https://doi.org/10.1017/s0016672308009579openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1038/35037572openalex-snapshot
The population genetics of ecological specialization in evolving Escherichia coli populations
inferredcites →https://doi.org/10.1038/35091062openalex-snapshot
Genetic linkage of ecological specialization and reproductive isolation in pea aphids
inferredcites →https://doi.org/10.1038/356519a0openalex-snapshot
Levels of naturally occurring DNA polymorphism correlate with recombination rates in D. melanogaster
inferredcites →https://doi.org/10.1038/4151022aopenalex-snapshot
Adaptive protein evolution in Drosophila
inferredcites →https://doi.org/10.1038/4151024aopenalex-snapshot
Testing the neutral theory of molecular evolution with genomic data from Drosophila
inferredcites →https://doi.org/10.1038/416531aopenalex-snapshot
The cost of inbreeding in Arabidopsis
inferredcites →https://doi.org/10.1038/scientificamerican1179-98openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1046/j.1365-2540.2000.00711.xopenalex-snapshot
Sexual isolation of genetically differentiated sympatric populations of Drosophila melanogaster in Brazzaville, Congo: the first step towards speciation?
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01491.xopenalex-snapshot
Single nucleotide polymorphisms derived from ancestral populations show no evidence for biased diversity estimates in Drosophila melanogaster
inferredcites →https://doi.org/10.1046/j.1471-8286.2003.00351.xopenalex-snapshot
microsatellite analyser (MSA): a platform independent analysis tool for large microsatellite data sets
inferredcites →https://doi.org/10.1073/pnas.061465098openalex-snapshot
The nucleotide changes governing cuticular hydrocarbon variation and their evolution in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.121418898openalex-snapshot
Incipient speciation by sexual isolation in Drosophila : Concurrent evolution at multiple loci
inferredcites →https://doi.org/10.1073/pnas.212248499openalex-snapshot
Molecular evidence for ecological speciation in tropical habitats
inferredcites →https://doi.org/10.1073/pnas.86.21.8442openalex-snapshot
Short-range genetic structure of Drosophila melanogaster populations in an Afrotropical urban area and its significance.
inferredcites →https://doi.org/10.1073/pnas.92.7.2519openalex-snapshot
Sexual isolation in Drosophila melanogaster: a possible case of incipient speciation.
inferredcites →https://doi.org/10.1086/284701openalex-snapshot
The Relative Rates of Evolution of Sex Chromosomes and Autosomes
inferredcites →https://doi.org/10.1086/303217openalex-snapshot
A Dynamical Theory of Speciation on Holey Adaptive Landscapes
inferredcites →https://doi.org/10.1093/genetics/144.2.635openalex-snapshot
Multi-Locus Selection and the Structure of Variation at the white Gene of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/147.3.1191openalex-snapshot
Incipient Speciation by Sexual Isolation in Drosophila melanogaster: Extensive Genetic Divergence Without Reinforcement
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/genetics/160.1.247openalex-snapshot
Chromosomal Patterns of Microsatellite Variability Contrast Sharply in African and Non-African Populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/160.2.595openalex-snapshot
Interactions Between Natural Selection, Recombination and Gene Density in the Genes of Drosophila
inferredcites →https://doi.org/10.1093/molbev/msg091openalex-snapshot
Genetic Differentiation Between American and European Drosophila melanogaster Populations Could Be Attributed to Admixture of African Alleles
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003804openalex-snapshot
Contrasting Patterns of X-Linked and Autosomal Nucleotide Variation in Drosophila melanogaster and Drosophila simulans
inferredcites →https://doi.org/10.1098/rspb.2000.1420openalex-snapshot
Gametic incompatibilities between races ofDrosophila melanogaster
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00707.xopenalex-snapshot
REPRODUCTIVE ISOLATION BETWEEN DIVERGENT RACES OF PEA APHIDS ON TWO HOSTS. II. SELECTION AGAINST MIGRANTS AND HYBRIDS IN THE PARENTAL ENVIRONMENTS
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb05657.xopenalex-snapshot
ESTIMATING F -STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE
inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb01257.xopenalex-snapshot
LABORATORY EXPERIMENTS ON SPECIATION: WHAT HAVE WE LEARNED IN 40 YEARS?
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb03965.xopenalex-snapshot
INCIPIENT SPECIATION BY SEXUAL ISOLATION INDROSOPHILA MELANOGASTER: VARIATION IN MATING PREFERENCE AND CORRELATION BETWEEN SEXES
inferredcites →https://doi.org/10.1186/1297-9686-25-6-517openalex-snapshot
Phenotypic and genetic variability of morphometrical traits in natural populations of Drosophila melanogaster and D simulans. I. Geographic variations
inferredcites →https://doi.org/10.1554/0014-3820(2001)055[0889:eotdog]2.0.co;2openalex-snapshot
EVOLUTION OF THERMAL DEPENDENCE OF GROWTH RATE OF ESCHERICHIA COLI POPULATIONS DURING 20,000 GENERATIONS IN A CONSTANT ENVIRONMENT

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/ece3.1335openalex-snapshot
Detecting a hierarchical genetic population structure: the case study of the Fire Salamander (Salamandra salamandra) in Northern Italy
inferred← citeshttps://doi.org/10.1007/s10592-016-0898-2openalex-snapshot
Population genetic structure and sex-biased dispersal of the hazel dormouse (Muscardinus avellanarius) in a continuous and in a fragmented landscape in central Italy
inferred← citeshttps://doi.org/10.1007/s10709-006-0006-5openalex-snapshot
Latitudinal clines for nucleotide polymorphisms in the Esterase 6 gene of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/s41437-021-00419-8openalex-snapshot
Low levels of genetic differentiation with isolation by geography and environment in populations of Drosophila melanogaster from across China
inferred← citeshttps://doi.org/10.1089/cmb.2005.12.1183openalex-snapshot
Algorithms for Selecting Informative Marker Panels for Population Assignment
inferred← citeshttps://doi.org/10.1093/molbev/msac223openalex-snapshot
Patterns of Population Structure and Introgression Among Recently Differentiated Drosophila melanogaster Populations
inferred← citeshttps://doi.org/10.1093/molbev/msi207openalex-snapshot
Inferring the Effects of Demography and Selection on Drosophila melanogaster Populations from a Chromosome-Wide Scan of DNA Variation
inferred← citeshttps://doi.org/10.1093/molbev/msv194openalex-snapshot
The Mosaic Ancestry of the Drosophila Genetic Reference Panel and the D. melanogaster Reference Genome Reveals a Network of Epistatic Fitness Interactions
inferred← citeshttps://doi.org/10.1101/2021.06.25.449842openalex-snapshot
Patterns of and processes shaping population structure and introgression among recently differentiated Drosophila melanogaster populations
inferred← citeshttps://doi.org/10.1101/340422openalex-snapshot
Early split between African and European populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2005.tb01778.xopenalex-snapshot
EVIDENCE OF SUSCEPTIBILITY AND RESISTANCE TO CRYPTIC X-LINKED MEIOTIC DRIVE IN NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2005.tb01821.xopenalex-snapshot
GEOGRAPHIC VARIATION IN DIAPAUSE INCIDENCE, LIFE‐HISTORY TRAITS, AND CLIMATIC ADAPTATION INDROSOPHILA MELANOGASTER
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2009.01318.xopenalex-snapshot
Parallels, nonparallels, and plasticity in population differentiation of threespine stickleback within a lake
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2004.02263.xopenalex-snapshot
World‐wide survey of anAccordinsertion and its association with DDT resistance inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2004.02422.xopenalex-snapshot
Population structure in African Drosophila melanogaster revealed by microsatellite analysis
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2005.02688.xopenalex-snapshot
Pre‐reproductive isolation as a consequence of allopatric differentiation between populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2006.03025.xopenalex-snapshot
Evidence of microsatellite hitch‐hiking selection in Atlantic cod (Gadus morhua L.): implications for inferring population structure in nonmodel organisms
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2006.03065.xopenalex-snapshot
Microsatellite variation and differentiation in African and non‐African populations of Drosophila simulans
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2008.03945.xopenalex-snapshot
QTL for the thermotolerance effect of heat hardening, knockdown resistance to heat and chill‐coma recovery in an intercontinental set of recombinant inbred lines of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04272.xopenalex-snapshot
Population genomics of marine fishes: identifying adaptive variation in space and time
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2004.00709.xopenalex-snapshot
An analysis of genetic differentiation among assortatively mating Drosophila melanogaster in Zimbabwe
inferred← citeshttps://doi.org/10.1111/j.1755-0998.2010.02943.xopenalex-snapshot
Application of SNPs for population genetics of nonmodel organisms: new opportunities and challenges
inferred← citeshttps://doi.org/10.1111/mec.13892openalex-snapshot
Continental‐level population differentiation and environmental adaptation in the mushroom S uillus brevipes
inferred← citeshttps://doi.org/10.1186/s12864-022-08839-4openalex-snapshot
Natural variation in the maternal and zygotic mRNA complements of the early embryo in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003080openalex-snapshot
Population Genomics of Sub-Saharan Drosophila melanogaster: African Diversity and Non-African Admixture
inferred← citeshttps://doi.org/10.1371/journal.pone.0001455openalex-snapshot
On the Origin and Spread of the Scab Disease of Apple: Out of Central Asia
inferred← citeshttps://doi.org/10.1371/journal.pone.0017358openalex-snapshot
Female Drosophila melanogaster Gene Expression and Mate Choice: The X Chromosome Harbours Candidate Genes Underlying Sexual Isolation
inferred← citeshttps://doi.org/10.1371/journal.pone.0026318openalex-snapshot
Genetic Diversity, Population Structure and Wolbachia Infection Status in a Worldwide Sample of Drosophila melanogaster and D. simulans Populations
inferred← citeshttps://doi.org/10.1534/genetics.104.037507openalex-snapshot
African Sequence Variation Accounts for Most of the Sequence Polymorphism in Non-AfricanDrosophila melanogaster
inferred← citeshttps://doi.org/10.1534/genetics.105.045831openalex-snapshot
Highly Structured AsianDrosophila melanogasterPopulations: A New Tool for Hitchhiking Mapping?
inferred← citeshttps://doi.org/10.1534/genetics.106.058693openalex-snapshot
History and Structure of Sub-Saharan Populations ofDrosophila melanogaster
inferred← citeshttps://doi.org/10.1534/genetics.106.063677openalex-snapshot
Identification of Selective Sweeps Using a Dynamically Adjusted Number of Linked Microsatellites
inferred← citeshttps://doi.org/10.1534/genetics.107.080200openalex-snapshot
AfricanDrosophila melanogasterandD. simulansPopulations Have Similar Levels of Sequence Variability, Suggesting Comparable Effective Population Sizes
inferred← citeshttps://doi.org/10.1534/genetics.112.146167openalex-snapshot
Surprising Differences in the Variability of Y Chromosomes in African and Cosmopolitan Populations ofDrosophila melanogaster
inferred← citeshttps://doi.org/10.1554/05-115.1openalex-snapshot
GEOGRAPHIC VARIATION IN DIAPAUSE INCIDENCE, LIFE-HISTORY TRAITS, AND CLIMATIC ADAPTATION IN DROSOPHILA MELANOGASTER
inferred← citeshttps://doi.org/10.1577/t08-165.1openalex-snapshot
Temporal Stability of Genetic Variation within Natural Populations of Summer Steelhead Receiving Mitigation Hatchery Fish
inferred← citeshttps://doi.org/10.6084/m9.figshare.21069711openalex-snapshot
Additional file 1 of Natural variation in the maternal and zygotic mRNA complements of the early embryo in Drosophila melanogaster
inferred← citeshttps://doi.org/10.6084/m9.figshare.21069717openalex-snapshot
Additional file 3 of Natural variation in the maternal and zygotic mRNA complements of the early embryo in Drosophila melanogaster
inferred← citeshttps://doi.org/10.70675/33889fbfz2424z41d8z86f4z7fa1c721ab39openalex-snapshot
Phylogeny and population genetics of the fish performing the largest migration known in freshwater, the Amazonian catfish "Brachyplatystoma rousseauxii" : revelations from the upper Madera Basin
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