EvolutionaryGenetics_01

  1. ASV
    • amplicon sequence variants
    • (ASV) is any one of the inferred single DNA sequences recovered from a high-throughput analysis of marker genes.
    • Because these analyses, also called "amplicon reads," are created
    • following the removal of erroneous sequences generated during PCR and sequencing, using ASVs makes it possible to distinguish sequence variation by a single nucleotide change.
  2. OTU
    • operational taxonomic unit
    • OTUs are employed in microbial community DNA sequencing research to
    • delineate species-level distinctions among organisms and represent the
    • most frequently utilized unit for measuring microbial diversity
    • In other words, OTUs are pragmatic proxies for "species" (microbial or metazoan) at different taxonomic levels, in the absence of traditional systems of biological classificationas are available for macroscopic organisms.
    • For several years, OTUs have been the most commonly used units of diversity, especially when analysing small subunit 16S (for prokaryotes) or 18S rRNA (for eukaryotes[5]) marker gene sequence datasets.
  3. Transitions vs. Transversions
    What are they, and which is more likely to occur, over time, evolutionary?
    • Transitions occur more frequently than transversions
    • Transitions are interchanges of purines (A-G) or pyrimdines (C-T), which involve bases of similar shape.
    • Transversions are interchanges between purine and pyrmidine bases, which involve exchange of one-ring and two-ring structures
  4. Transitions
    • Transitions are interchanges of purines (A-G) or pyrimdines (C-T), which involve bases of similar shape.
    • Image Upload 2
  5. Transversion
    • Transversions are interchanges between purine and pyrmidine bases, which involve exchange of one-ring and two-ring structures
    • Image Upload 4
  6. bifurcation
    branching pattern typical in phylogenies
  7. reticulation
    • when species recombine and create a net like pattern in phylogenies
    • Image Upload 6
  8. what are different modes of reproduction seen in phylogenies?
    • asexual (clonal)
    • sexual (recombination)
    • combination of the two
  9. Method for inferring structure and process in populations:
    Non-genealogical (frequency-based)
    • Classical Wright’s FST statistics
    • Neutrality tests (Tajima, Fu)
    • Genetic Diversity measures (Nei)
    • Population subdivision (Hudson)
    • Population parameter estimators (θ)
    • Compatibility methods (Le Quesne)
  10. Method for inferring structure and process in populations:
    Genealogical (single tree)
    • Wright’s FST estimators (Slatkin)
    • Neutrality tests (Fu and Li)
    • Haplotype phenotype association testing
    • Phylogeography
  11. Method for inferring structure and process in populations:
    Genealogical (random trees)
    • Coalescent approaches (parameter estimation: θ , recombination, migration rates)   (Beerli and Felsenstein)
    • Bayesian approaches (Hey and Nielsen)
    • Probability distributions of mutations for different phenotypic categories (Griffiths and Tavaré)
    • Equilibrium and non-equilibrium models
  12. Method for inferring structure and process in populations; give an example of each:
    Non-parametric
    mixed
    Parametric
    • Non-parametric: Hardy-Weinberg (simple model)
    • mixed: Wright-Fisher
    • Parametric: coalescence (complex model)
  13. Which category of inferring structure/process in populations is this:
    Classical Wright's FST statistics
    Non-genealogical (frequency based)
  14. Which category of inferring structure/process in populations is this:
    Neutrality tests (Tajima, Fu)
    Non-genealogical (frequency based)
  15. Which category of inferring structure/process in populations is this:
    Genetic Diversity measures (Nei)
    Non-genealogical (frequency based)
  16. Which category of inferring structure/process in populations is this:
    Population subdivision (Hudson)
    Non-genealogical (frequency based)
  17. Which category of inferring structure/process in populations is this:
    Population parameter estimators (θ)
    Non-genealogical (frequency based)
  18. Which category of inferring structure/process in populations is this:
    Compatibility methods (Le Quesne)
    Non-genealogical (frequency based)
  19. Which category of inferring structure/process in populations is this:
    Wright's Fst estimators (Slatkin)
    Genealogical (single tree)
  20. Which category of inferring structure/process in populations is this:
    Neutrality tests (Fu and Li)
    Genealogical (single tree)
  21. Which category of inferring structure/process in populations is this:
    Haplotype phenotype association testing
    Genealogical (single tree)
  22. Which category of inferring structure/process in populations is this:
    phylogeography
    Genealogical (single tree)
  23. Which category of inferring structure/process in populations is this:
    Coalescent approaches (parameter estimation: θ, recombination, migration rates)- Beerli and Felsenstein
    Genealogical (random trees)
  24. Which category of inferring structure/process in populations is this:
    Bayesian approaches (Hey and Nielsen)
    Genealogical (random trees)
  25. Which category of inferring structure/process in populations is this:
    Probability distributions for mutations for different phenotypic categories (Griffiths and Tavare)
    Genealogical (random trees)
  26. Which category of inferring structure/process in populations is this:
    Equilibrium and non-equilibrium models
    Genealogical (random trees)
  27. Neutral mutation rate (μ)
    the number of neutral mutations arising in an individual per nucleotide site (10^9) or per gene per unit time
  28. Effective population size (Ne)
    the number of interbreeding individuals in a population having the same magnitude of random genetic drift as the actual population, but never exceeding the actual population size
  29. Define the population neutral mutation rate (θ) for diploids
    • θ = 4Ne µ
    • Some properties of θ = 4Ne µ
    •   If we assume a neutral mutation rate of 2 x 10-9 mutations per site per year, then Ne can be estimated from θ
  30. What are assumptions of Tajima's D?
    D=X/(√var(x))
    X = k – (s / (1 + 1/2 + 1/3 + ... + 1/n-1))
    • Constant population size (i.e. equilibrium)
    • Infinite-sites compatible, no recombination, no migration
Author
saucyocelot
ID
365935
Card Set
EvolutionaryGenetics_01
Description
notes from the first few lectures
Updated