<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(11)</volume><submitter>Spencer HG</submitter><pubmed_abstract>Simple models of viability selection acting on variation at a single diploid locus only maintain multiple alleles for very restricted sets of fitnesses. Most of these models assume that fitnesses are independent, even if the genotypes share alleles. Here, we extend this result to a model with generalized dominance interactions, in which fitnesses are strongly affected by what we call the "primary effects" of the genotype's component alleles, so that genotypes with shared alleles have correlated fitnesses. Nevertheless, in keeping with previously reported results, we also show that such fitness sets are easily constructed over time if recurrent mutation is occurring simultaneously. We find that such models maintain less variation over time than do (previous) models with independently sample</pubmed_abstract><journal>G3 (Bethesda, Md.)</journal><pagination>3725-3732</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5100871</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Selective Maintenance of Allelic Variation Under Generalized Dominance.</pubmed_title><pmcid>PMC5100871</pmcid><pubmed_authors>Spencer HG</pubmed_authors><pubmed_authors>Mitchell C</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Selective Maintenance of Allelic Variation Under Generalized Dominance.</name><description>Simple models of viability selection acting on variation at a single diploid locus only maintain multiple alleles for very restricted sets of fitnesses. Most of these models assume that fitnesses are independent, even if the genotypes share alleles. Here, we extend this result to a model with generalized dominance interactions, in which fitnesses are strongly affected by what we call the "primary effects" of the genotype's component alleles, so that genotypes with shared alleles have correlated fitnesses. Nevertheless, in keeping with previously reported results, we also show that such fitness sets are easily constructed over time if recurrent mutation is occurring simultaneously. We find that such models maintain less variation over time than do (previous) models with independently sample</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Nov</publication><modification>2025-04-22T08:58:47.612Z</modification><creation>2019-03-27T02:28:34Z</creation></dates><accession>S-EPMC5100871</accession><cross_references><pubmed>27652891</pubmed><doi>10.1534/g3.116.028076</doi></cross_references></HashMap>