Question

In: Statistics and Probability

Neurofibromatosis Type 1 (NF1) is a human genetic disorder. As well as physical symptoms, affected children...

Neurofibromatosis Type 1 (NF1) is a human genetic disorder. As well as physical symptoms, affected children often suffer from impaired cognition and learning. A cognitive task that involves solving a puzzle is administered to a group of children. For each child the time taken (in seconds) to solve the task is recorded.

It is not known whether there is any suitable parametric model for the times so we will investigate non-parametric methods.


1. Calculate appropriate summary statistics and thus give the parameters for a normal distribution that may be applicable to these data.

2. Using the observed data, calculate the empirical distribution function. Plot the empirical distribution function and the CDF of the normal distribution described in (a) on a single graph.

3. Do you think the normal distribution is an appropriate model for the data? Justify your answer.

It is known that the mean time to solve the puzzle in healthy control children is 60 seconds.

The data for the observed times ?? taken by 57 children with NF1 are:

ID yi
1 51
2 60
3 75
4 43
5 92
6 72
7 49
8 39
9 62
10 127
11 51
12 75
13 69
14 59
15 25
16 58
17 95
18 63
19 91
20 63
21 32
22 50
23 108
24 41
25 93
26 43
27 74
28 50
29 55
30 60
31 62
32 91
33 79
34 71
35 85
36 86
37 78
38 100
39 146
40 62
41 134
42 41
43 40
44 51
45 68
46 59
47 59
48 38
49 66
50 79
51 111
52 69
53 68
54 110
55 69
56 62
57 91

Solutions

Expert Solution


Related Solutions

Neurofibromatosis Type 1 (NF1) is a human genetic disorder. As well as physical symptoms, affected children...
Neurofibromatosis Type 1 (NF1) is a human genetic disorder. As well as physical symptoms, affected children often suffer from impaired cognition and learning. A cognitive task that involves solving a puzzle is administered to a group of children. For each child the time taken (in seconds) to solve the task is recorded. It is not known whether there is any suitable parametric model for the times so we will investigate non-parametric methods. Carry out the Wilcoxon signed-rank test on these...
describe the cellular events that are affected in one genetic disorder that is the result of...
describe the cellular events that are affected in one genetic disorder that is the result of either point or chromosomal mutation
Signs and Symptoms of Pregnancy Provide the implications of the given disorder as well as the...
Signs and Symptoms of Pregnancy Provide the implications of the given disorder as well as the nursing actions or interventions I Presumptive Cause/ Physiologic basis Nursing Action/s in the Care of clients 1) amenorrhea 2) nausea & vomiting 3) urinary frequency 4) breast changes & tenderness 5) excessive fatigue 6) uterine enlargement 7) quickening II Probable changes Cause/ Physiologic basis Nursing Implication/s 1) changes in pelvic organs -Goodell sign -Hegar sign -Piskacek sign 2) (+) HCG 3)Uterine souffle 4) Skin...
7. A genetic disorder occurs with probability 1/2000 . There is a test for this genetic...
7. A genetic disorder occurs with probability 1/2000 . There is a test for this genetic disorder. If you have the disorder, then you test positive 90% of the time. If you don’t have the disorder, then you test negative 90% of the time. If you test positive, what is the probability that you have the disorder?
Thalassemia is a genetic disorder where affected individuals have red blood cells that produce too much...
Thalassemia is a genetic disorder where affected individuals have red blood cells that produce too much iron. This disease is inherited as an autosomal recessive (tt). However, heterozygous individuals (carriers= Tt) may have some immunity to malaria (similar to sickle cell anaemia). Human blood samples are obtained from a Mediterranean population of 100 people where malaria is endemic. Of these, 50 people are found to be carriers (Tt), and additional 3 people have thalassemia (tt). Use these observed results to...
In a dominant x-linked genetic disorder, what sex could be affected? Explain in details your answer...
In a dominant x-linked genetic disorder, what sex could be affected? Explain in details your answer citing all possibilities.
1. Gillespie syndrome (GS) is a rare genetic disorder. The disorder is characterized by having part...
1. Gillespie syndrome (GS) is a rare genetic disorder. The disorder is characterized by having part of the iris missing, ataxia, and, in most cases, intellectual disability. It is termed as a heterogenous disorder because it can be inherited either through an autosomal dominant pattern or through an autosomal recessive pattern. Two parents are heterozygous for GS. A. Assuming that the condition is following an autosomal dominant pattern, what are the ratios or percentages of the genotypes AND phenotypes for...
Please write a short essay on Sjögren’s syndrome: •Type of disorder and symptoms •Lab test methods...
Please write a short essay on Sjögren’s syndrome: •Type of disorder and symptoms •Lab test methods •Lab test result interpretation •Treatment
Characterize the symptoms associated with: 1) illness anxiety disorder, 2) panic disorder, and 3) somatic symptom...
Characterize the symptoms associated with: 1) illness anxiety disorder, 2) panic disorder, and 3) somatic symptom disorder. Describe areas of overlap among these three disorders and their distinguishing features. What role does anxiety play in the development and maintenance of each of these disorders? If different, how are the underlying anxiety issues addressed in the treatment of these disorders?
Learning Task 18-02: Genetic Disorders Research and write a brief description of each genetic disorder. 1-...
Learning Task 18-02: Genetic Disorders Research and write a brief description of each genetic disorder. 1- Huntington Disease 2- Tay-Sachs Disease 3-Marfan Syndrome 4- Cystic Fibrosis 5-Duchenne Muscular Dystrophy For each disease, state the chances that a child would be born with the disease: if one parent carries the gene; and if both parents carry the gene. Explain how you arrived at your answers. Use Punnett squares to help justify your response for each disease.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT