Midterm 1 Flashcards

(42 cards)

1
Q

Population Genetics

A

The study of genetic composition of a population and processes that shape the composition.

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2
Q

What is the common goal of population genetics research?

A

To deduce process from composition.

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3
Q

What is a population?

A

A group of individuals of the same species that occupy an area.

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4
Q

What is genetic composition?

A

Genotype counts, genotype frequencies, nucleotide frequencies, haplotype freq., others.

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5
Q

Genotype Counts

A

Number of genotypes in the population.

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6
Q

What are the processes that effect genetic compisition?

A
  • Selection, mutation, random genetic drift, dispersal/migration
  • Recombination, horizontal gene transfer, insertions/deletions
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7
Q

MIC

A

Minimum inhibitory concentration
- Lowest of the antibiotic yielding no
visible growth

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8
Q

MSC

A

Minimum selective concentration
- [ ] of antibiotic that resistant and
susceptible genotypes have equal
fitness - where the lines cross

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9
Q

Traditional Selective Window

A

Range of antibiotic concentrations
considered high enough, such that
resistant genotype outcompetes susceptible

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10
Q

Sub-MIC Selective Window

A

Additional range of antibiotic concentrations when resistant genotype outcompetes susceptible.

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11
Q

Absolute Fitness

A

A parameter that predicts (or predicts in part) the growth in numbers of a generatio.

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12
Q

What is the difference between growth rate (r), and absolute fitness (λ)

A

Growth Rate (r) - Continuous
Absolute Fitness (λ) - Finite rate of increase, discrete time.

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13
Q

Relative Fitness (ω)

A

Absolute fitness of a genotype divided by the absolute fitness of a standard (reference) genotype.

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14
Q

Selection coefficient (s)

A

Proportional increase (s>0) or decrease (s<0) in relative fitness of a genotype relative to the reference.

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15
Q

MSC occurs when s = ?
resistant and susceptible genotypes have ____ fitness

A

s = 0
resistant and susceptible genotypes have EQUAL fitness

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16
Q

Where would you observe MSC on a graph?

A

Where the line crosses line on graph or where the two lines transect

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17
Q

Population Structure

A

The nonrandom distribution of genotypes geographically due to limited dispersal or local adaptation.

18
Q

Geographic variation in frequency is an indicator of ____ because…

A

Population structure because it shows limited dispersal.

19
Q

What is segregating site (S)

A

A nucleotide site in a sample that is variable

20
Q

Balancing Selection

A

Two or more genotypes selectively maintained in a population.
- Build up of mutations along deep branches increases π = lots of pairwise differences
- negative frequency dependent selection

21
Q

Selective Sweep

A

Recent beneficial genotype arises and rapidly increases.
- short time scale
- unique mutations
- few pairwise differences (nucleotide differences are small)

22
Q

π - S/a > 0

A

Balancing Selection
- a = the summation of 1/k

23
Q

π - S/a < 0

A

Selective Sweep
- a = the summation of 1/k

24
Q

π - S/a = 0

25
In an ancestral recombination graph upstream goes...
Left
26
In an ancestral recombination graph downstream goes...
Right
27
Recombination can result in _____ coalescent histories for _____ regions of the genome
different
28
Describe Model-based gene tree estimation and it's goal
Model-Based - ML - Bayesian Goal: Estimate history if common descent Share ancestor w each-other before sharing ancestor w other lineages.
29
Distance-based gene tree estimation
Distance-based - UPGMA - Neighbour-joining Goal: Cluster sequences based on genetic similarity Genetically more similar to each other compared to other lineages
30
What is more probable: a transition or a transversion?
Transition is more probable than transversion.
31
T or F: for teo lineages to coalesce they must be in the same deme?
True
32
Do we expect genotypes sampled in the same deme to coalesce with each other first, before coalescing with genotypes sampled in a different deme when: N<
Yes
33
Do we expect genotypes sampled in the same deme to coalesce with each other first, before coalescing with genotypes sampled in a different deme when: N > T, m = 0
No
34
Do we expect genotypes sampled in the same deme to coalesce with each other first, before coalescing with genotypes sampled in a different deme when: N < T, m = 0.1
No
35
Random Genetic Drift
Changes in genotypes frequencies due to random sampling in finite populations.
36
Explain the birth death process
1. Random individual gives birth 2. Random individual dies
37
Explain how gene trees can be used to detect recombination across the genome of a population of viruses
If different regions of a genime have different coalescent histories, then this is evidence for recombination between regions
38
can individuals coalesce while they are in different demes?
No
39
Explain why we expect drift to be greater in small versus large populations
There is a greater change in genotype frequency in when you add or remove one genotype in small populations which is consistent with drift being greater.
40
Why do we expect selection to be more efficient in a large versus a small population?
In smaller populations a decrease by 1 copy lowers the frequency of the genotype to a greater extent than the larger population which is going against the direction of selection.
41
Why is it the extremes of genotype frequencies produce similar probabilities of not changing during a birth death event?
Because when a genotype is at high frequency, it is likely to be picked both to reproduce and die during a birth death event, so genotype frequencies are not expected to change too much
42
Why are intermediate frequencies a lower probability of unchanging during a birth death event?
This is because when a genotype is an intermediate fequency, it is more likely that a different genotype is chosen to reproduce versus die, so genotype frequencies are more likely to change.