scholarly article | Q13442814 |
P50 | author | Douglas Kell | Q5301676 |
David C. Wedge | Q39451750 | ||
Mark Platt | Q57058803 | ||
P2093 | author name string | William Rowe | |
Philip J Day | |||
Joshua Knowles | |||
P2860 | cites work | Architecture of ribosomal RNA: constraints on the sequence of "tetra-loops" | Q24556605 |
Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase | Q27860794 | ||
In vitro selection of RNA molecules that bind specific ligands | Q27861109 | ||
Rational evolutionary design: the theory of in vitro protein evolution | Q28142227 | ||
Diversity and complexity in DNA recognition by transcription factors | Q29619632 | ||
Exploring the sequence space of a DNA aptamer using microarrays | Q33304953 | ||
Prediction of hybridization and melting for double-stranded nucleic acids | Q34186238 | ||
Defining the sequence-recognition profile of DNA-binding molecules | Q34304813 | ||
Empirical fitness landscapes reveal accessible evolutionary paths | Q34606034 | ||
Generalized topological spaces in evolutionary theory and combinatorial chemistry. | Q34709744 | ||
Oligonucleotide inhibitors of human thrombin that bind distinct epitopes | Q36890950 | ||
Analysis of aptamer sequence activity relationships | Q38347807 | ||
Array-based evolution of DNA aptamers allows modelling of an explicit sequence-fitness landscape | Q38358691 | ||
The NK model of rugged fitness landscapes and its application to maturation of the immune response | Q42643980 | ||
Towards a general theory of adaptive walks on rugged landscapes | Q47593883 | ||
Approximate scaling properties of RNA free energy landscapes. | Q52298965 | ||
From sequences to shapes and back: a case study in RNA secondary structures. | Q52379672 | ||
Error Detecting and Error Correcting Codes | Q55871133 | ||
P433 | issue | 44 | |
P304 | page(s) | 397-408 | |
P577 | publication date | 2009-07-22 | |
P1433 | published in | Journal of the Royal Society Interface | Q2492390 |
P1476 | title | Analysis of a complete DNA-protein affinity landscape | |
P478 | volume | 7 |
Q54474794 | A thousand empirical adaptive landscapes and their navigability. |
Q41986173 | Adaptation in tunably rugged fitness landscapes: the rough Mount Fuji model |
Q46070825 | Analysis of in vitro evolution reveals the underlying distribution of catalytic activity among random sequences. |
Q36217511 | Beyond the Hypercube: Evolutionary Accessibility of Fitness Landscapes with Realistic Mutational Networks |
Q38218962 | Empirical fitness landscapes and the predictability of evolution |
Q34005257 | Evolutionary accessibility of mutational pathways |
Q42365796 | Evolutionary algorithms and synthetic biology for directed evolution: commentary on "on the mapping of genotype to phenotype in evolutionary algorithms" by Peter A. Whigham, Grant Dick, and James Maclaurin |
Q28710543 | Exploiting genomic knowledge in optimising molecular breeding programmes: algorithms from evolutionary computing |
Q51610625 | Genome structure and the benefit of sex |
Q92342787 | Genotype network intersections promote evolutionary innovation |
Q42689235 | Hidden specificity in an apparently nonspecific RNA-binding protein |
Q37184676 | How Good Are Statistical Models at Approximating Complex Fitness Landscapes? |
Q64940140 | Mapping a Systematic Ribozyme Fitness Landscape Reveals a Frustrated Evolutionary Network for Self-Aminoacylating RNA. |
Q26752642 | Methods for Improving Aptamer Binding Affinity |
Q30424517 | Naturally selecting solutions: the use of genetic algorithms in bioinformatics |
Q21145317 | Predictability of evolutionary trajectories in fitness landscapes |
Q35079781 | Properties of selected mutations and genotypic landscapes under Fisher's geometric model. |
Q35077513 | Quantifying the similarity of monotonic trajectories in rough and smooth fitness landscapes |
Q55379339 | RNA-mediated gene regulation is less evolvable than transcriptional regulation. |
Q42135811 | Scientific discovery as a combinatorial optimisation problem: how best to navigate the landscape of possible experiments? |
Q59142935 | Selective Phenome Growth Adapted NK Model: A Novel Landscape to Represent Aptamer Ligand Binding |
Q27316616 | Sort-seq under the hood: implications of design choices on large-scale characterization of sequence-function relations |
Q26796990 | Specificity and nonspecificity in RNA-protein interactions |
Q38287400 | Synthetic biology for the directed evolution of protein biocatalysts: navigating sequence space intelligently |
Q55002438 | The Influence of Higher-Order Epistasis on Biological Fitness Landscape Topography. |
Q52314365 | The architecture of an empirical genotype-phenotype map. |
Q58570246 | The causes of evolvability and their evolution |
Q54310563 | The robustness and evolvability of transcription factor binding sites. |
Q24289511 | Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson’s, Huntington’s, Alzheimer’s, prions, bactericides, chemical toxicology and others as examples |
Q41365190 | Tunably Rugged Landscapes With Known Maximum and Minimum |
Q34190107 | Visualizing fitness landscapes |
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