Week 10 Flashcards

1
Q

forces of genetic variation

A

Variation arises by mutation
Distribution of variation occurs because of genetic drift, migration and natural selection (dependent on effective population size Ne)
In total, four forces

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

hardy-wienburg

A

Species is one randomly mating group
No evolutionary forces acting
Models relationship between allele and genotype frequencies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

HW helps us identify:

A

Deviations from random mating
Finite population size (bottlenecks, genetic drift)
Inbreeding
It is a null model

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

three main properties of HW

A

Allele frequencies do not change from one generation to the next (no evolution)
Genotypes are 100% reliably predictable from allele frequencies
A single generation of random mating is sufficient to return genotype frequencies to H-W expectations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

how do we test if data fits HW?

A

Chi-squared test - compares. The observed genotype counts with expected under HW
d.f is calculated with number of possible genotypes - number of alleles
Chi allows us to see if the difference between observed and expected is significant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

f statistics

A

Measuring the amount and direction of deviation from HW proportions
Measures genetic variation at different levels in the hierarchy of biological organisation (individuals, subpopulations and populations)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what does Fis tell us?

A

Whether individuals in subpopulations mate approximately at random in their subpopulation
It measures inbreeding
Measures how the variation within individuals (heterozygosity) compares to that in their subpopulation (average heterozygosity in subpopulation)
If the levels of heterozygosity are the same, the subpopulation is panmictic (randomly mating)
It DOES NOT measure heterozygosity or homozygosity (that’s what heterozygosity is for)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Fis range

A

From -1 to +1
Excessively high proportion of heterozygotes compared to HW = negative (deficient homozygous proportion)
Excessively homozygous compared to HW = positive
0 = expected proportions by HW

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

when data differs from HW, what might be untrue?

A

Random mating
No natural selection
No mutation
Infinite population size
No immigration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

HW vs the real world

A

HW assumes allele frequencies do not change between generations (no evolution)
This assumes random mating and none of the four evolutionary forces are acting
This is often untrue in the real world

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

drivers of negative Fis

A

non-random mating - disassortative mating (unlike types mate, active outbreeding)
Immigration
Small population size (chance deviations)
Selection (balancing selection)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

drivers of positive fis

A

Non-random mating due to population genetic structure (Wahlund effect)
Non-random mating due to assortative mating (mating with like, inbreeding)
Immigration is too recent for random mating
Small population causing chance deviations
Selection is directional

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

types of mating systems

A

Random
Assortative/inbreeding/selfing/cloning
Disassortative/outbreeding/inbreeding avoidance
Polygyny/monogamy/promiscuity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

dispersal that causes gene flow

A

Long-distance/short distance
Sex-biased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

population genetic structure

A

How genetic similarity is distributed in space and time
Random mating, isolation by distance, fragmented, cline etc.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

genotypic arrays

A

Individual and population signatures of genetic variation
Even though alleles at all loci are found in both places, Ireland and Hungary have different characteristics
Considering the combination of genetic variation over many loci is powerful
Information arrises from correlations of different alleles at different loci
Some combinations are more common and some are less common (not random)
Tells us about reproductive modes and heaps more!

17
Q

linkage disequilibrium

A

Combinations of alleles at different loci are more likely to appear than other combinations

18
Q

genetic parentage analysis

A

Helps understand mating systems
Mate choice
Allocation of parental care
Inbreeding avoidance
Reproductive function
Likelihood proposed that a relationship is true (can work out who true father is)

19
Q

genetic clustering analysis

A

Structure does two main tasks: determines the number of demes and finds what extent an individual fits in each deme (cluster membership value called q values)
Show us gene flow and migration patterns

20
Q

assignment tests

A

Estimate the population origin of an individual
Gives us a probability signal
More powerful with more loci

21
Q

what does dispersal do? how can it be measured?

A

Drives demographic and genetic connectivity
Brings genetic variation
Critical but hard to estimate
Can be measured with collars, tags, GPS, radio trackers
Direct genetic estimates of dispersal and gene flow can be down with parentage and assignment tests