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Biology
Paper 3
topic 7
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Cards (68)
Chi-squared
is one of the three statistics that need to be known for
A-level
biology
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Chi-squared
Used to investigate whether there is a
difference
between
frequency
data
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If you are
not
confident on chi-squared, there is a
first
video that goes through all the details
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Using chi-squared for inheritance questions
1. Work out expected frequency using
Punnett
square
2. Record
observed
frequency
3. Calculate
chi-squared
statistic
4. Compare chi-squared value to
critical
value
5. Accept or reject
null
hypothesis
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Null hypothesis
There is
no
significant difference between the expected and
observed frequency
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You don't need to calculate
chi-squared
in the exam, you would just be given the value or
p-value
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Inheritance example - corn kernels
Expected
75
% purple,
25
% yellow
Observed
21
purple,
13
yellow
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Steps to use chi-squared for corn kernel example
1. Calculate expected frequencies
2. Calculate chi-squared statistic
3. Determine degrees of freedom
4. Compare chi-squared value to critical value
5. Accept or reject null hypothesis
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If chi-squared value does not exceed critical value, there is more than 5% probability the results are due to chance
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Accepting the null hypothesis means there is
no significant difference between expected and observed frequencies
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Using
chi-squared
shows the
corn kernels
followed the expected 3:1 ratio, proving Mendelian genetics
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Epistasis
When one
gene
influences the
expression
of another one
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Epistasis questions will always be
dihybrid
examples because it's to do with two genes and one gene
masking
the expression of the other
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Examples of epistasis
Cake color in mice
Color in
labradors
Color of certain
squash
fruits
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Inheritance of labrador fur color
1.
Gene
1 controls whether pigment is expressed
2.
Gene
2 controls which pigment is expressed
3. Possible
gametes
4. Punnett square to determine
genotypes
and
phenotypes
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If a labrador has two copies of the
recessive
e
allele
They will be
yellow
in color
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If a labrador has a
dominant
b allele
They will be
black
in
color
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If a
labrador
has a recessive b
allele
They will be
brown
in color
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The ratio of phenotypes in the labrador example is
9
:
4
:3
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Pedigree diagram
Circles
represent females
Squares
represent males
Colors
indicate fur color
Genotypes
of some individuals are provided
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Determining
genotypes
from a pedigree
diagram
1. Start by
filling
in what you can
identify
straight away
2. Look at
parents
/offspring to determine missing
alleles
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Gene 1 in squash fruit color
Dominant allele
inhibits
an enzyme needed to make squash green or yellow, resulting in
white
fruit
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Gene 2 in squash fruit color
Dominant
allele codes for an enzyme that functions normally to make the squash yellow,
recessive
allele results in green fruit
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Determining squash fruit color phenotype from genotypes
Use the
flow diagram
to determine the effect of the two
genes
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The
squash fruit color
example is another example of epistasis
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Dominant
An
allele
that will always be
expressed
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Recessive
Alleles
which are only expressed if there isn't a
dominant
one present
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Genotype
The
genetic
composition of the
organism
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Phenotype
The characteristic of an organism due to expression of the
genotype
and the
environment
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Gene
A small section of
DNA
which could code for a
polypeptide
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Alleles
Alternative
forms of one
gene
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Dihybrid
Looking at the
inheritance
of two genes within the same
Punnett
square
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Mendelian
genetics
Genetics based on the work of
Gregor Mendel
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Gene 1 (shape)
Round
(dominant) or
wrinkled
(recessive)
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Gene
2
(colour)
Yellow
(dominant) or
green
(recessive)
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Dihybrid cross
1. Label parent
phenotypes
2. Determine parent
genotypes
3. Identify possible
gametes
4. Combine
gametes
to get offspring genotypes
5. Determine offspring
phenotypes
6. Calculate
phenotype ratios
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When crossing a
homozygous dominant
parent with a homozygous recessive parent, all the
F1
offspring will be heterozygous
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Crossing F1 heterozygous offspring
1. Identify all possible
gamete
combinations
2. Use a
Punnett
square to determine offspring genotypes
3. Determine offspring
phenotypes
4. Calculate
phenotype
ratios (9:3:3:1)
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Autosomal linkage
Two
genes are located on the same
chromosome
(not a sex chromosome)
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Autosomal linkage
Reduces the number of possible
gamete
combinations, leading to a different
phenotype
ratio (e.g. 3:1)
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