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How many genes? Mapping mouse traits, cont.

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Denoting the two markers by 1 and 2, the NOD alleles by a, ... Here P and M denote the Paternally and Maternally transmitted haplotypes, respectively. ... – PowerPoint PPT presentation

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Title: How many genes? Mapping mouse traits, cont.


1
How many genes? Mapping mouse traits, cont.
  • Lecture 2B, Statistics 246
  • January 22, 2004

2
Lets estimate the recombination fraction r
between D12Mit51 and D12Mit132
132 51 A H B Total
A 26 10 0 36
H 10 46 9 65
B 0 5 23 28
Total 36 61 32 129

2-locus genotypes at D12Mit51 and D12Mit132. 129
offspring from H?H, where A?B?H.
3
Estimation of r
  • First note that we cant simply count
    recombinants. Why? Because recombination can
    occur in the paternal or the maternal meiosis, or
    both, and all we see are the genotypes of the
    offspring. In most cases, the parental origin of
    the recombination can be inferred, but not in
    every case.
  • Denoting the two markers by 1 and 2, the NOD
    alleles by a,
  • and B6 alleles by b, then the parental
    haplotypes are a1a2 on one chromosome, and b1b2
    on the other. Each parent passes on a1a2 with
    probability(1-r)/2, and similarly for b1b2 ,
    while they pass on each of the recombinant
    haplotypes a1b2 and b1a2 with probability r/2.
  • In practice, recombinations have slightly
    different frequencies in male and female meioses,
    but we ignore this refinement.

4
Probabilities of parentally transmitted haplotype
combinations (?4)
  • Haplotype combinations resulting from
    crossing doubly heterozygous parents, each a1/b1
    at locus 1 and a2/b2 at locus 2. This table is
    for coupling the parental haplotypes are a1a2
    and b1b2, i.e. the mother and father are both
    a1a2/b1b2.
  • Here P and M denote the Paternally and
    Maternally transmitted haplotypes, respectively.

P M a1a2 a1b2 b1a2 b1b2
a1a2 (1-r)2 r(1-r) r(1-r) (1-r)2
a1b2 r(1-r) r2 r2 r(1-r)
b1a2 r(1-r) r2 r2 r(1-r)
b1b2 (1-r)2 r(1-r) r(1-r) (1-r)2

5
From the Punnett square to the table of
2-locus genotype probabilities
  • Terms in the Punnett square table can be summed
    to build up a table of probabilities for the 9
    different 2-locus genotype probabilities.
  • For example, we observe A (a1/a1 ) at locus 1
    and H (a2 /b2) at locus 2, if and only if the
    transmitted male and female haplotypes are the
    pairs a1a2 a1b2 or a1b2 a1a2 , and this occurs
    with a combined probability of 2r(1-r)/4.
  • The other terms are built up similarly, the
    most complex case being the 2-locus genotype HH,
    where 4 different terms need to be considered,
    corresponding to the fact that a double
    heterozygote can result from 4 different
    combinations of parental or recombinant
    haplotypes.

6
Probabilities of 2-locus genotypes (?4)
L1 L2 A H B
A (1-r)2 2r(1-r) r2
H 2r(1-r) 2r2(1-r)2 2r(1-r)
B r2 2r(1-r) (1-r)2
Looking at this table, we see that recombinations
(or not) can be inferred, apart from the
parent, in all but the HH case. We can almost
count recombinants.
7
Estimation of r, cont.
  • Using the table of probabilities we can write
    down a log likelihood function for any set of
    2-locus frequencies.
  • Label the cells of the table 1,,9, and denote
    the corresponding probabilities by p1(r) ,.p9
    (r), and the frequencies by n1, , n9. Then the
    log-likelihood for the resulting multinomial
    model is
  • log L ?i ni log pi (r).
  • The parameter r is then estimated by maximizing
    this function, and an approximate standard error
    or confidence interval obtained using the Fisher
    information or the asymptotic chi-square
    approximation.

8
A frill the M-step of an EM-algorithm
  • The function log L(r) can be maximized in a
    number of ways, but in general there is no closed
    form expression for the maximum likelihood
    estimate r. If we were able to decompose the
    count n5 of HHs into the n5P that are pairs of
    parental haplotypes, and n5R that are pairs of
    recombinant haplotypes, with frequencies (1-r)2
    and r2, resp, the recombinant haplotypes can then
    be counted directly and the MLE is
  • 2(n3 n7 n5R) n2 n4 n6
    n8)/2n.

9
The E-step
  • In general we dont know n5R but can estimate
    it using the following formula
  • In practice, we need a value of r to begin
    with. Next we use the above estimate, then get
    the next , and then iterate.
  • Exercise Prove the above formula, and that
    the iteration is an instance of the EM-algorithm.

10
2-locus genotype frequencies for D12Mit132 and
D13Mit6
132 6 A H B Total
A 10 21 7 38
H 15 29 17 61
B 5 21 6 32
Total 30 71 30 131

Exercise Estimate r for these two loci. Is it
different from 1/2?
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