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Widespread selection against deleterious mutations in the Drosophila genome

https://doi.org/10.1101/2020.02.12.946392
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Mathematical Population Genetics : I. Theoretical Introduction
inferredcites →https://doi.org/10.1007/978-1-4613-0931-4_4openalex-snapshot
Historical Biogeography of the Drosophila melanogaster Species Subgroup
inferredcites →https://doi.org/10.1007/bf00275839openalex-snapshot
Frequency spectra of neutral and deleterious alleles in a finite population
inferredcites →https://doi.org/10.1007/bf02459575openalex-snapshot
Evolution in mendelian populations
inferredcites →https://doi.org/10.1016/0040-5809(72)90035-4openalex-snapshot
The sampling theory of selectively neutral alleles
inferredcites →https://doi.org/10.1016/0040-5809(75)90020-9openalex-snapshot
On the number of segregating sites in genetical models without recombination
inferredcites →https://doi.org/10.1016/j.tig.2011.06.003openalex-snapshot
Weighing the evidence for adaptation at the molecular level
inferredcites →https://doi.org/10.1016/j.tree.2010.04.001openalex-snapshot
Approximate Bayesian Computation (ABC) in practice
inferredcites →https://doi.org/10.1016/s0040-5809(02)00050-3openalex-snapshot
Maximum likelihood and Bayesian methods for estimating the distribution of selective effects among classes of mutations using DNA polymorphism data
inferredcites →https://doi.org/10.1017/cbo9780511623486openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1017/s0016672300014634openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1017/s0016672300033619openalex-snapshot
The effect of recombination on background selection
inferredcites →https://doi.org/10.1017/s0305004100033193openalex-snapshot
Random processes in genetics
inferredcites →https://doi.org/10.1038/246096a0openalex-snapshot
Slightly Deleterious Mutant Substitutions in Evolution
inferredcites →https://doi.org/10.1038/nature04107openalex-snapshot
Adaptive evolution of non-coding DNA in Drosophila
inferredcites →https://doi.org/10.1038/nrg2146openalex-snapshot
The distribution of fitness effects of new mutations
inferredcites →https://doi.org/10.1038/nrg3454openalex-snapshot
Exploring the three-dimensional organization of genomes: interpreting chromatin interaction data
inferredcites →https://doi.org/10.1038/scientificamerican1179-98openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1093/bfgp/elu038openalex-snapshot
Functional roles of nucleosome stability and dynamics
inferredcites →https://doi.org/10.1093/genetics/105.2.437openalex-snapshot
EVOLUTIONARY RELATIONSHIP OF DNA SEQUENCES IN FINITE POPULATIONS
inferredcites →https://doi.org/10.1093/genetics/114.2.525openalex-snapshot
THE ORGANIZATION OF GENETIC VARIATION FOR RECOMBINATION IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1093/genetics/123.4.887openalex-snapshot
The "hitchhiking effect" revisited.
inferredcites →https://doi.org/10.1093/genetics/132.4.1161openalex-snapshot
Population genetics of polymorphism and divergence.
inferredcites →https://doi.org/10.1093/genetics/138.1.227openalex-snapshot
Selection intensity for codon bias.
inferredcites →https://doi.org/10.1093/genetics/141.4.1605openalex-snapshot
Deleterious background selection with recombination.
inferredcites →https://doi.org/10.1093/genetics/155.3.1405openalex-snapshot
Hitchhiking Under Positive Darwinian Selection
inferredcites →https://doi.org/10.1093/genetics/159.4.1779openalex-snapshot
Directional Selection and the Site-Frequency Spectrum
inferredcites →https://doi.org/10.1093/genetics/162.1.203openalex-snapshot
Testing Models of Selection and Demography in Drosophila simulans
inferredcites →https://doi.org/10.1093/genetics/162.4.2025openalex-snapshot
Approximate Bayesian Computation in Population Genetics
inferredcites →https://doi.org/10.1093/genetics/69.1.71openalex-snapshot
MODIFICATION OF RECOMBINATION FREQUENCY IN DROSOPHILA. I. SELECTION FOR INCREASED AND DECREASED CROSSING OVER
inferredcites →https://doi.org/10.1093/genetics/69.1.85openalex-snapshot
MODIFICATION OF RECOMBINATION FREQUENCY IN DROSOPHILA. II. THE POLYGENIC CONTROL OF CROSSING OVER
inferredcites →https://doi.org/10.1093/genetics/76.3.447openalex-snapshot
SELECTION FOR REDUCED CROSSING OVER IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1093/molbev/msw195openalex-snapshot
A Thousand Fly Genomes: An Expanded Drosophila Genome Nexus
inferredcites →https://doi.org/10.1093/nar/gky1003openalex-snapshot
FlyBase 2.0: the next generation
inferredcites →https://doi.org/10.1098/rstb.2009.0278openalex-snapshot
Genetic hitchhiking versus background selection: the controversy and its implications
inferredcites →https://doi.org/10.1098/rstb.2010.0106openalex-snapshot
Genetic linkage and natural selection
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb00188.xopenalex-snapshot
THE ECOLOGY AND GENETICS OF FITNESS IN CHLAMYDOMONAS. XII. REPEATED SEXUAL EPISODES INCREASE RATES OF ADAPTATION TO NOVEL ENVIRONMENTS
inferredcites →https://doi.org/10.1146/annurev.genom.1.1.539openalex-snapshot
Methods to Detect Selection in Populations with Applications to the Human
inferredcites →https://doi.org/10.1371/journal.pcbi.1002803openalex-snapshot
Approximate Bayesian Computation
inferredcites →https://doi.org/10.1371/journal.pcbi.1004845openalex-snapshot
Deep Learning for Population Genetic Inference
inferredcites →https://doi.org/10.1371/journal.pgen.1000495openalex-snapshot
Pervasive Natural Selection in the Drosophila Genome?
inferredcites →https://doi.org/10.1371/journal.pgen.1002905openalex-snapshot
The Many Landscapes of Recombination in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1003090openalex-snapshot
Genome-Wide Fine-Scale Recombination Rate Variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1003527openalex-snapshot
Strong Purifying Selection at Synonymous Sites in D. melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1004434openalex-snapshot
Background Selection as Baseline for Nucleotide Variation across the Drosophila Genome
inferredcites →https://doi.org/10.1371/journal.pone.0190186openalex-snapshot
Generalization of the Ewens sampling formula to arbitrary fitness landscapes
inferredcites →https://doi.org/10.1534/genetics.105.048223openalex-snapshot
Approximate Bayesian Inference Reveals Evidence for a Recent, Severe Bottleneck in a Netherlands Population of Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.111.134288openalex-snapshot
The Effects of Deleterious Mutations on Evolution at Linked Sites
inferredcites →https://doi.org/10.1534/genetics.113.151670openalex-snapshot
Rates and Genomic Consequences of Spontaneous Mutational Events in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.113.158758openalex-snapshot
Estimation of the Spontaneous Mutation Rate per Nucleotide Site in a Drosophila melanogaster Full-Sib Family
inferredcites →https://doi.org/10.1534/genetics.115.174664openalex-snapshot
The Drosophila Genome Nexus: A Population Genomic Resource of 623 Drosophila melanogaster Genomes, Including 197 from a Single Ancestral Range Population
inferredcites →https://doi.org/10.4171/owr/2005/40openalex-snapshot
Mathematical Population Genetics
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