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true as opposed to an estimated pop measure |
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an estimate of a paramter using a sample of a total pop |
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Example of parameter vs stat |
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PARAM *height of female adult in US -would have a true mean and variance -hard to determine
STAT *estimate by using female in class -calc mean and variance but would not give a true value -estimate mean(mu-cap) and estimated variance (σ^2-cap) |
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Statistics used for a sample |
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TO ESTIMATE MEAN * Mu-cap = sum / n
TO ESTIMATE VARIANCE/ COV * σ^2-cap = (average of the deviations^2) but w/ n-1 |
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*correction for error in estimated value *hard to make denominator smaller to account for the fact that the numerator is smaller (so won't have a biased ratio) *deviations between e. ind data point and mu-cap is smaller than the deviation between e. sample & the true mean (mu) |
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tracks samples (moves closer to the majority) |
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relationship between mu and mu-cap |
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[Σ(xi - mu-cap)^2] < {Σ(xi- mu)^2}
*[dev between sample and mu-cap] is a systematic underestimate of the {deviation between the sample and Mu} b/c the estimate comes from the samples |
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*to describe quant traits (measured on numerical scale) *allows to answer questions, work w/ quant trait, & see patterns of inheritance, etc when you cant tell geno *gives framework to describe how a pop will respond to a particular scenario & what the best strat would be |
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*describes why "best pheno" doesnt always mean best genetics b/c quant traits are affected by genetics and env *helps describe quant traits
P = Mu + G + E
P: pheno value Mu: pop mean G: geno value E: env effect
Values ==> P, G, E Pop Measure ==> Mu |
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How to define the genetic merit of a quant trait |
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DETERMINE IND GENO VALUE W/ CLONES *AKA: how an ind geno influences own pheno value *clone an ind and grow in same env as original *P will vary among clones b/c they all have env effects (but mean env effects, E-bar, = 0)
DETERMINE IND GENETIC MERIT W/ BREEDING *AKA: how geno of ind influence pheno of progeny *if a bull has lots of progeny, their P can tell about parental genetics *plan: cross e. bull to many random cows from pop & evaluate the offspring from these crosses |
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*organism w/ same genetics *every position in the genome is the same |
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mean phrno of progeny of an ind, compared to the pop
Mu pop pheno (daught) - Mu pop pheno (original) |
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*the effect of the env on a particular trait for a specific ind *can't control |
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BV = 2(PD)
*true only if PD is the real PD -needs to account for random effects, so no small pop *2 b/c any given progeny has only 1/2 genetics from a particular parent |
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relationship between PD and BV |
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* Mu pheno of clones is 2x Mu pheno of progeny *geno value determined from clones is same as BV |
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*predicted transmitting ability *can't be seen, but can colelct lots of info and predict it *measure of genetic merit
1/2BV = PD = TA
PTA = EPD = 1/2BV-cap |
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*estimated progeny difference *for beef industry, 1/2 estimated BV of a ind |
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relationship between G determined through clones and BV determined by progeny |
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G(CLONES) = BV(PROGENY) *assuming no dominance ==> heteros are intermediate, and e. loci behaves independently w/ additivity *b/c a fundamental description of genetics for a quant trait
G(CLONES) ≠ BV(PROGENY) *assuming dominance/epistasis *G(XX) = G(Xx) : b/c they influence the pheno of ind the same and have same pheno value -BUT from a breeding perspective, G(XX) more valuable b/c has 2 X to pass on |
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*ind BV relative to the pop mean (Mu) *combo of 2 components |
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1) Assume single locus -determine if dom/epistasis, no dominance
2) No env influence -E=0 (so dont need to make clones)
3) Define P
4) Define allele freq and geno
5) Find pop mean (Mu) -Mu = [f(XX) * P(XX)] + [f(Xx) * P(Xx)] + [f(xx) * P(xx)]
6) Find G - P = Mu + G + E
7) Find BV -find the PD --> BV = 2(PD) |
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*accounts for differences between G and BV *more specific to P = Mu + [BV + GCV] + E
BV + GCV = G G: geno value BV: breeding value; sum of ind allelic effects, additive genetic effect GCV: gene combination value; NOT TRANSMITTED, non additive genetic effect |
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*genetic combination value (allele combination value) *non-additive gene effect due to combo of alleles -EX: dominace interaction *dev between G and BV *not passed on to generations b/c comes from combo of alleles that sep during meiosis (due to law of seg) -only 1 is put into a gene and passed on (parents pass alleles, not genes) |
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*due to Law of Seg, a parent does not give its geno (only passes on alleles) -so the way a parents geno influences the pheno value of offspring is diff than the way a pheno value influence its own
*BV = G w/o dom and/or epistasis - w/ dom and epistasis, the interactions influence P of ind w/ that geno, but are not transmitted to next gen and dont influence P of offspring
P = Mu + G + E *G represents how ind geno represents own pheno value *G does not describe how ind geno influences pheno value of offspring (BV) |
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important property of the genetic model |
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*used to think about quant traits ==> revels behavior of traits and best breeding strats |
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trait w/o env influence (E=0 for all ind) |
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P = Mu + G G = P - Mu
*the consequence of having P-bar makes it so G is expressed as dev from mean which makes G-bar = 0 |
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trait w genetic and env influence |
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P = Mu + G + E
*need to assume that G (GCV + BV), and E are independent of e.other -so G of ind is random w/ respect to env effect that the ind experiences
*if G and E are independent [COV(G,E)=0] then G-bar = 0 and E-bar = 0
*the factors that influence P (i.e G, E, etc) are independent and combo of G + E = 0 |
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