Pregunta 1
Pregunta
What type of chromosome does G-banding "line-up"?
Respuesta
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Metaphase
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Anaphase
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Telophase
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Prophase
Pregunta 2
Pregunta
What stain does G-banding use?
Respuesta
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Giemsa
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Chrome red
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Methyl-blue
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Green
Pregunta 3
Pregunta
G-banding can only detect large abnormalities. True or false?
Pregunta 4
Pregunta
What does FISH stand for?
Respuesta
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Fluorescent in situ hybridization
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Fluorescent in site hydrolysis
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Familial in situ hybridization
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Familial in situ hydrolysis
Pregunta 5
Pregunta
You don't need to know what abnormality you are looking for when using FISH. True or false?
Pregunta 6
Pregunta
Why do you need to know what abnormality you are looking for when using FISH?
Pregunta 7
Pregunta
How can you tell if there is an abnormality using the FISH technique?
Respuesta
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Because some of the markers will not light up as they have not been able to anneal to bits of DNA sequence as they are missing
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Because all of the markers will light up because there are specific sequences of DNA that cause genetic disorders
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Because if there were no abnormalities the markers would not show up at all
Pregunta 8
Pregunta
FISH can show slightly smaller abnormalities than G-banding, but they still have to fairly large. True or false?
Pregunta 9
Pregunta
What does QF-PCR stand for?
Respuesta
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Quantitative fluorescence Polymerase Chain Reaction
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Qualitative fluorescence polymerase chain reaction
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Quantitative familial polymerase chain reaction
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Qualitative familial polymerase chain reaction
Pregunta 10
Pregunta
What is QF-PCR used to detect?
Pregunta 11
Pregunta
What is the name for trisomy 13?
Respuesta
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Pattau's syndrome
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Edward's syndrome
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Down's syndrome
Pregunta 12
Pregunta
What is the name for trisomy 18?
Respuesta
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Pattau's syndrome
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Edward's syndrome
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Down's syndrome
Pregunta 13
Pregunta
What is the name for trisomy 21?
Respuesta
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Pattau's syndrome
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Edward's syndrome
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Down's syndrome
Pregunta 14
Pregunta
Which biological technique is quickest?
Pregunta 15
Pregunta
You have to know what abnormality you are looking for when using QF-PCR. True or false?
Pregunta 16
Pregunta
What sort of abnormalities does array-CGH detect?
Respuesta
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Larger abnormalities
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Smaller abnormalities
Pregunta 17
Pregunta
What is DNA labelled with in array-CGH?
Respuesta
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Fluorescent dye
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Coloured markers
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Radiation
Pregunta 18
Pregunta
What does the CGH in array-CGH stand for?
Respuesta
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Comparative genomic hybridization
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Comparative genomic hydrolysis
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Comparative genetic hybridization
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Comparative genetic hydrolysis
Pregunta 19
Pregunta
How can you tell if there is an abnormality in the DNA when using array-CGH?
Respuesta
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The relative fluorescence of the sample and control strand will be different
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The relative radiation of the sample and control strand will be different
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The length of the sample and control strand will be different when run through gel electrophoresis
Pregunta 20
Pregunta
Which two molecular biological techniques look at the actual base sequence when looking for genetic abnormalities?
Pregunta 21
Pregunta
Which of the following is cheaper and less time consuming?
Pregunta 22
Pregunta
Why do we only sequence exons when using sanger sequencing?
Respuesta
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Because the introns do not code for proteins so are not important to us
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Because it is time consuming and expensive
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Because introns rarely have mutations that cause genetic diseases
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Because we are unable to isolate the introns to sequence them
Pregunta 23
Pregunta
What machine is used in sanger sequencing to read the sequence of bases?
Respuesta
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An electropheragram
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A Geiger counter
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A microscope
Pregunta 24
Pregunta
Not all changes to the base sequence cause disease. True or false?
Pregunta 25
Pregunta
Why is it better to use next generation sequencing when you don't know what you are looking for?
Respuesta
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Because it is easy to sequence a whole genome
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Because sanger sequencing would take too long
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Because next generation sequencing is more accurate
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Because next generation sequencing is less expensive