All Stories

  1. The order in which amino acids were added to the genetic code in ancient life
  2. Extinction vortices are driven more by a shortage of beneficial mutations than by deleterious mutation accumulation
  3. The protein domains of vertebrate species in which selection is more effective have greater intrinsic structural disorder
  4. The protein domains of vertebrate species in which selection is more effective have greater intrinsic structural disorder
  5. The protein domains of vertebrate species in which selection is more effective have greater intrinsic structural disorder
  6. Order of amino acid recruitment into the genetic code resolved by Last Universal Common Ancestor’s protein domains
  7. Background Selection From Unlinked Sites Causes Nonindependent Evolution of Deleterious Mutations
  8. Enhanced testing can substantially improve defence against several types of respiratory virus pandemic
  9. Combatting SARS-CoV-2 With Digital Contact Tracing and Notification: Navigating Six Points of Failure
  10. Optimal targeting of interventions uses estimated risk of infectiousness to control a pandemic with minimal collateral damage
  11. A Mechanistically Integrated Model of Exploitative and Interference Competition over a Single Resource Produces Widespread Coexistence
  12. Human deleterious mutation rate implies high fitness variance, with declining mean fitness compensated by rarer beneficial mutations of larger effect
  13. A new codon adaptation metric predicts vertebrate body size and tendency to protein disorder
  14. Combatting SARS-CoV-2 With Digital Contact Tracing and Notification: Navigating Six Points of Failure (Preprint)
  15. Differential Retention of Pfam Domains Contributes to Long-term Evolutionary Trends
  16. The protein domains of vertebrate species in which selection is more effective have greater intrinsic structural disorder
  17. The effectiveness of selection in a species affects the direction of amino acid frequency evolution
  18. Differential retention of Pfam domains creates long-term evolutionary trends
  19. Random Peptides Rich in Small and Disorder-Promoting Amino Acids Are Less Likely to Be Harmful
  20. Genetics of adaptation and fitness landscapes: From toy models to testable quantitative predictions
  21. nQMaker: Estimating Time Nonreversible Amino Acid Substitution Models
  22. Background selection from unlinked sites causes non-independent evolution of deleterious mutations
  23. Substitution load revisited: a high proportion of deaths can be selective
  24. The economic value of quarantine is higher at lower case prevalence, with quarantine justified at lower risk of infection
  25. Differences in evolutionary accessibility determine which equally effective regulatory motif evolves to generate pulses
  26. Quantifying meaningful usage of a SARS-CoV-2 exposure notification app on the campus of the University of Arizona
  27. Universal and taxon-specific trends in protein sequences as a function of age
  28. Differences in evolutionary accessibility determine which equally effective regulatory motif evolves to generate pulses
  29. The economic value of quarantine is higher at lower case prevalence, with quarantine justified at lower risk of infection
  30. Mutation bias can shape adaptation in large asexual populations experiencing clonal interference
  31. The protein domains of vertebrate species in which selection is more effective have greater intrinsic structural disorder
  32. Quantifying SARS-CoV-2 infection risk within the Google/Apple exposure notification framework to inform quarantine recommendations
  33. Only a Single Taxonomically Restricted Gene Family in the Drosophila melanogaster Subgroup Can Be Identified with High Confidence
  34. Random peptides rich in small and disorder-promoting amino acids are less likely to be harmful
  35. Evolution Rapidly Optimizes Stability and Aggregation in Lattice Proteins Despite Pervasive Landscape Valleys and Mazes
  36. Universal and taxon-specific trends in protein sequences as a function of age
  37. Mutation bias can shape adaptation in large asexual populations experiencing clonal interference
  38. High Transcriptional Error Rates Vary as a Function of Gene Expression Level
  39. Density-dependent selection and the limits of relative fitness
  40. Evolution rapidly optimizes stability and aggregation in lattice proteins despite pervasive landscape valleys and mazes
  41. Readthrough errors purge deleterious cryptic sequences, facilitating the birth of coding sequences
  42. Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
  43. Biomarkers for aging identified in cross-sectional studies tend to be non-causative
  44. Different mechanisms drive the maintenance of polymorphism at loci subject to strong versus weak fluctuating selection
  45. High transcriptional error rates vary as a function of gene expression level
  46. A Shift in Aggregation Avoidance Strategy Marks a Long-Term Direction to Protein Evolution
  47. Directional Selection Rather Than Functional Constraints Can Shape the G Matrix in Rapidly Adapting Asexuals
  48. Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
  49. Gene Birth Contributes to Structural Disorder Encoded by Overlapping Genes
  50. Directional selection rather than functional constraints can shape the G matrix in rapidly adapting asexuals
  51. Reply to Cheong et al.: Unicellular survival precludes Parrondo’s paradox
  52. Intercellular competition and the inevitability of multicellular aging
  53. A shift in aggregation avoidance strategy marks a long-term direction to protein evolution
  54. Young genes are highly disordered as predicted by the preadaptation hypothesis of de novo gene birth
  55. Drift Barriers to Quality Control When Genes Are Expressed at Different Levels
  56. Drift barriers to quality control when genes are expressed at different levels
  57. Answering evolutionary questions: A guide for mechanistic biologists
  58. What Fraction of Duplicates Observed in Recently Sequenced Genomes Is Segregating and Destined to Fail to Fix?
  59. Constraints on the evolution of phenotypic plasticity: limits and costs of phenotype and plasticity
  60. Cryptic genetic variation can make “irreducible complexity” a common mode of adaptation in sexual populations
  61. CHANCE, PURPOSE, AND PROGRESS IN EVOLUTION AND CHRISTIANITY
  62. Q&A: Evolutionary capacitance
  63. Compensatory Evolution and the Origins of Innovations
  64. Rethinking Hardy–Weinberg and genetic drift in undergraduate biology
  65. Hsp90 depletion goes wild
  66. Protein stickiness, rather than number of functional protein-protein interactions, predicts expression noise and plasticity in yeast
  67. The consequences of rare sexual reproduction by means of selfing in an otherwise clonally reproducing species
  68. Genetic drift
  69. Evolution of molecular error rates and the consequences for evolvability
  70. Putatively Noncoding Transcripts Show Extensive Association with Ribosomes
  71. Robustness and Evolvability
  72. The Spontaneous Appearance Rate of the Yeast Prion [PSI+] and Its Implications for the Evolution of the Evolvability Properties of the [PSI+] System
  73. Robustness: mechanisms and consequences
  74. THE EVOLUTION OF REVERSIBLE SWITCHES IN THE PRESENCE OF IRREVERSIBLE MIMICS
  75. Quantitative Prediction of Molecular Clock and Ka/Ks at Short Timescales
  76. Complex Adaptations Can Drive the Evolution of the Capacitor [PSI+], Even with Realistic Rates of Yeast Sex
  77. The Strength of Selection Against the Yeast Prion [PSI+]
  78. The evolution of bet-hedging adaptations to rare scenarios
  79. A Bayesian model of quasi-magical thinking can explain observed cooperation in the public good game
  80. The Roles of Mutation Accumulation and Selection in Loss of Sporulation in Experimental Populations ofBacillus subtilis
  81. The Loss of Adaptive Plasticity during Long Periods of Environmental Stasis
  82. Mutations Leading to Loss of Sporulation Ability in Bacillus subtilis Are Sufficiently Frequent to Favor Genetic Canalization
  83. The Conversion of 3′ UTRs into Coding Regions
  84. THE POPULATION GENETICS OF PHENOTYPIC DETERIORATION IN EXPERIMENTAL POPULATIONS OF BACILLUS SUBTILIS
  85. Cryptic Genetic Variation Is Enriched for Potential Adaptations
  86. THE POPULATION GENETICS OF PHENOTYPIC DETERIORATION IN EXPERIMENTAL POPULATIONS OF BACILLUS SUBTILIS
  87. Evolutionary Capacitance May Be Favored by Natural Selection
  88. Efficient Inhibition of Prion Replication by PrP-Fc2 Suggests that the Prion is a PrPSc Oligomer
  89. Prion Kinetics
  90. THE EVOLUTION OF THE EVOLVABILITY PROPERTIES OF THE YEAST PRION [PSI+]
  91. THE EVOLUTION OF THE EVOLVABILITY PROPERTIES OF THE YEAST PRION [PSI+]
  92. The measured level of prion infectivity varies in a predictable way according to the aggregation state of the infectious agent
  93. Designing drugs to stop the formation of prion aggregates and other amyloids
  94. Quantifying the kinetic parameters of prion replication
  95. Topological structures for 4-dimensional geographic information systems