scholarly article | Q13442814 |
P50 | author | Daniel S. Fisher | Q1162465 |
P2093 | author name string | B I Shraiman | |
R A Neher | |||
P2860 | cites work | IS THE POPULATION SIZE OF A SPECIES RELEVANT TO ITS EVOLUTION? | Q22065713 |
Sex increases the efficacy of natural selection in experimental yeast populations | Q22122472 | ||
Sex releases the speed limit on evolution | Q22122522 | ||
The evolutionary advantage of recombination | Q24533419 | ||
Beneficial mutation selection balance and the effect of linkage on positive selection | Q24685465 | ||
High-resolution mapping of meiotic crossovers and non-crossovers in yeast | Q27938210 | ||
Is the population size of a species relevant to its evolution? | Q28215741 | ||
Why sex and recombination? | Q28283292 | ||
Linkage and the limits to natural selection | Q28769449 | ||
Recombination speeds adaptation by reducing competition between beneficial mutations in populations of Escherichia coli | Q33294903 | ||
Modeling and optimization of populations subject to time-dependent mutation | Q33958359 | ||
A ruby in the rubbish: beneficial mutations, deleterious mutations and the evolution of sex | Q33963090 | ||
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Deleterious mutations and the evolution of sexual reproduction | Q34164458 | ||
Evolution of human immunodeficiency virus under selection and weak recombination | Q34573357 | ||
Selection for recombination in structured populations | Q34587456 | ||
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Sex and adaptation in a changing environment | Q34607998 | ||
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Evolution of recombination in a constant environment | Q36403048 | ||
The stochastic edge in adaptive evolution | Q36665927 | ||
Competition between recombination and epistasis can cause a transition from allele to genotype selection | Q37167732 | ||
Emergent gene order in a model of modular polyketide synthases | Q37429055 | ||
The traveling-wave approach to asexual evolution: Muller's ratchet and speed of adaptation | Q41853709 | ||
Evolution of recombination due to random drift | Q42128822 | ||
The Hill-Robertson effect and the evolution of recombination | Q42421139 | ||
Recombination can evolve in large finite populations given selection on sufficient loci. | Q42533089 | ||
Requisite mutational load, pathway epistasis and deterministic mutation accumulation in sexual versus asexual populations | Q46070628 | ||
Analytic approach to the evolutionary effects of genetic exchange | Q48456956 | ||
The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
Deleterious mutations as an evolutionary factor: 1. The advantage of recombination | Q56341012 | ||
The evolution of sex and recombination in a varying environment | Q70503881 | ||
A general model for the evolution of recombination | Q71859154 | ||
The effect of linkage on limits to artificial selection | Q72951099 | ||
RNA virus evolution via a fitness-space model | Q74568198 | ||
Increasing sequence correlation limits the efficiency of recombination in a multisite evolution model | Q79397025 | ||
Recombination dramatically speeds up evolution of finite populations | Q81561012 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 467-481 | |
P577 | publication date | 2009-11-30 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | Rate of adaptation in large sexual populations | |
P478 | volume | 184 |
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Q34804767 | Estimate of effective recombination rate and average selection coefficient for HIV in chronic infection |
Q42741265 | Evolution of Mutation Rates in Rapidly Adapting Asexual Populations. |
Q35105761 | Fifteen years later: hard and soft selection sweeps confirm a large population number for HIV in vivo |
Q57069104 | Fitness variation in isogenic populations leads to a novel evolutionary mechanism for crossing fitness valleys |
Q36154425 | Fluctuations of fitness distributions and the rate of Muller's ratchet. |
Q36535424 | Genealogies of rapidly adapting populations |
Q54691706 | Genes under weaker stabilizing selection increase network evolvability and rapid regulatory adaptation to an environmental shift. |
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Q22065128 | Genetic draft and quasi-neutrality in large facultatively sexual populations |
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Q33895065 | How to infer relative fitness from a sample of genomic sequences |
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Q30555815 | Rate of adaptation in sexuals and asexuals: a solvable model of the Fisher-Muller effect |
Q48521753 | Recombination Alters the Dynamics of Adaptation on Standing Variation in Laboratory Yeast Populations. |
Q92638300 | Recombination and mutational robustness in neutral fitness landscapes |
Q24634833 | Robustness and evolvability |
Q28749184 | Scaling expectations for the time to establishment of complex adaptations |
Q51723842 | Sex drives intracellular conflict in yeast. |
Q41410650 | Stronger selection can slow down evolution driven by recombination on a smooth fitness landscape. |
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Q37875514 | The contribution of statistical physics to evolutionary biology. |
Q37269691 | The dynamics of genetic draft in rapidly adapting populations |
Q37948449 | The many costs of sex. |
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Q35377813 | The route of HIV escape from immune response targeting multiple sites is determined by the cost-benefit tradeoff of escape mutations |
Q35247990 | The time scale of evolutionary innovation |
Q90571692 | Understanding the evolution of interspecies interactions in microbial communities |
Q36354246 | What can ecosystems learn? Expanding evolutionary ecology with learning theory. |
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