F1 and F2 offspring with given genders and disease phenotypes. The data are generated from an initial parental cross. One parent displays the disease phenotype and one displays the wild-type (WT) phenotype. The WT parent always has a homozygous genotype. There are three possible modes of inheritance that underlie the generation of the data. All are monogenic. They are: (i)   Autosomal Recessive. (ii)  Homozygous Lethal Dominant. (iii) Autosomal Dominant. One's phenotype is determined by their genotype at the disease locus and the mode of inheritance, as we have seen with Punnett Square. on the F2 data and make a decision, based on your statistical analysis, as to whether you reject or do not reject the computer-generated model of inheritance as being consistent with the observed data. The mode of inheritance you are to test on the observed data is autosomal recessive. PARENTAL CROSS   Parental cross: Father with disease phenotype, Mother with wild-type phenotype.   F1 DATA   Phenotype Gender Disease     Wild-Type   Male        49                 0 Female       61               0   F2 DATA   Phenotype Gender Disease       Wild-Type   Male         39           15 Female.       45           11 Gender Phenotype Observed counts     (O) Expected Proportions Expected Counts     (E) (O-E) (O-E)^2/E Male WT           Male Disease           Female WT           Female Disease           Total                       DegFrdm             P-value   In typed please with calculations.

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F1 and F2 offspring with given genders and disease phenotypes.

The data are generated from an initial parental cross.

One parent displays the disease phenotype and one displays the wild-type (WT) phenotype.

The WT parent always has a homozygous genotype.

There are three possible modes of inheritance that underlie

the generation of the data. All are monogenic. They are:

(i)   Autosomal Recessive.

(ii)  Homozygous Lethal Dominant.

(iii) Autosomal Dominant.

One's phenotype is determined by their genotype at the disease locus

and the mode of inheritance, as we have seen with Punnett Square.

on the F2 data and make a decision, based on your statistical analysis, as to whether

you reject or do not reject the computer-generated model of inheritance as being consistent

with the observed data.

The mode of inheritance you are to test on the observed data is autosomal recessive.



PARENTAL CROSS

 

Parental cross: Father with disease phenotype, Mother with wild-type phenotype.

 

F1 DATA

 

Phenotype

Gender Disease     Wild-Type

  Male        49                 0

Female       61               0

 

F2 DATA

 

Phenotype

Gender Disease       Wild-Type

  Male         39           15

Female.       45           11

Gender

Phenotype

Observed counts 

   (O)

Expected

Proportions

Expected Counts

    (E)

(O-E)

(O-E)^2/E

Male

WT

         

Male

Disease

         

Female

WT

         

Female

Disease

         

Total

           
         

DegFrdm

 
         

P-value

 

In typed please with calculations. 


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