Question 1

Why is there still a need for conventional karyotyping using chromosome banding techniques?

Accepted Answer

Conventional karyotyping using chromosome banding is nevertheless still clinically important. That is so because molecular genetic methods such as array CGH are not suited to detecting balanced chromosome rearrangements in which there is no net gain or loss of DNA. Balanced translocations and inversions would normally be invisible to these methods, but they can be detected by chromosome banding.

Question 2

Concerning preimplantation genetic diagnosis, which, if any, of the following statements is incorrect?
a) It is carried out within the context of assisted reproduction.
b) The analyses always involve genotyping just a single cell and so are technically difficult.
c) Sometime a single blastomere is analysed from the embryo.
d) Sometimes a polar body is analysed to infer the genotype of the embryo.

Accepted Answer

b) The analyses always involve genotyping just a single cell and so are technically difficult.
d) Sometimes a polar body is analysed to infer the genotype of the embryo.

Question 3

Mutation scanning and mutation testing can be used to identify pathogenic mutations. What is the essential difference between these two approaches?

Accepted Answer

In mutation scanning, the object is to seek out any candidate pathogenic mutations in a defined region of DNA (usually an exon or gene), or even in an exome or genome, without having prior knowledge of the nature of the pathogenic mutation(s). For example, DNA sequencing assays can identify changes in a desired DNA region, exome or genome. By looking at how the DNA sequence differs from reference sequences candidate pathogenic mutations can be identified, such as obviously inactivating mutations in coding DNA in the case of recessive disorders.
In mutation testing, the object is to identify a defined DNA change at a specific location in the DNA, usually a well-studied mutation. For example, we might wish to test a cystic fibrosis patient for the p.Phe508del mutation in the CFTR gene.

Question 4

What are the main uses of chromosome fluorescence in situ hybridization in a genetic service laboratory?

Accepted Answer

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Question 5

A genetic test for a marker M was carried out in 500 people affected by disease X and showed that 480 of the affected individuals typed positive for the marker. In a suitably matched set of 1000 healthy controls, just 80 people typed positive for marker.
i) Establish the sensitivity and specificity of the test.
ii) Work out the false positive rate and the positive predictive value
iii) Work out the false negative rate and the negative predictive value.

Accepted Answer

The answer of A genetic test for a marker M...

Question 6

Interpret the following DNA and amino acid variants:
a) c.*15A>G
b) p.Asp522del
c) c.-22T>G
d) c.121-6C>A

Accepted Answer

The answer of Interpret the following DNA and amino acid...

Question 7

Concerning prenatal diagnosis, which, if any, of the following statements is false?
a) It relies on surgical procedures to recover fetal tissues from a pregnant woman.
b) Chorion villus biopsies are typically taken around 16 weeks of gestation.
c) Amniotic fluid samples allow culturing of fetal cells for cytogenetic analyses as well as allowing DNA analyses.
d) There is always a small excess risk of miscarriage.

Accepted Answer

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Question 8

What is involved in chromosome fluorescence in situ hybridization?

Accepted Answer

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Question 9

Concerning genetic screening, which, if any, of the following statements is false?
a) Genetic screening is carried out primarily in communities and populations
b) In carrier screening the motivation is to identify carriers of a mutant allele for a severe autosomal recessive disorder that has a high prevalence in the community or population.
c) In most cases of pregnancy screening the motivation is to identify whether a fetus carries a genetic variant associated with a harmful single gene disorder.
d) In newborn screening the motivation is often to target early treatment for serious disorders for which early intervention can make a significant difference.

Accepted Answer

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Question 10

Match the disorder
a) to h) with the likelihood that it would be a focus for a genetic procedure listed in i) to vi)

Accepted Answer

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a) to h) with the...

Question 11

What are the main applications of Southern blot-hydridization as an assay in a genetics service laboratory?

Accepted Answer

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Question 12

Fill in the blanks below with single words.
Traditional ______ diagnosis has involved _____2______ surgical procedures in which a sample of fetal cells is recovered and analysed. There have been two major approaches. In one case a sample is taken from the _____3____ (the outermost extra-embryonic ____4_____ ). Typically this sample is taken in the ____5______ trimester of pregnancy. In the other case, a sample of _____6_____ fluid is taken that will contain cells from the _____7______ , an inner extra-embryonic ____4_____. This procedure, called ____8_____ is taken at, or close to, 16 weeks of gestation; it provides fetal cells that can be processed to allow ____9_____ analyses as well as DNA analyses. Because of the surgical procedures involved there is a small excess risk of ____10_____. As a result, there has been a trend to develop non-_____2______ ______ diagnosis. That has been fuelled by _______ 2______ sequencing of DNA from maternal ____13____.

Accepted Answer

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Question 13

What is the basis of the ACCE framework for genetic testing?

Accepted Answer

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Question 14

Multiplex ligation-dependent probe amplifaction (MLPA) is an important technology used in genetics research and genetic testing. What uses is it put to in a genetics service laboratory and what is the basis of the method.

Accepted Answer

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Question 15

Fill in the blanks below with single words.
______ genetic diagnosis is carried out in the contact of assisted reproduction. It can be technically challenging because quite often analysis is carried out on a ____2_____ cell, that may be from the early stage _____3____ (the stage at which the embryo consists of just a very few cells that are individually called ____4_____ ). Another alternative, that can be used when the mother is at risk of transmitting a harmful genetic variant, is to infer the genotype of the _____5_____ by analysing a ____6____ ____7_____ (a cell that is created by one of the asymmetric cell divisions in female ____8_____). Because of technical difficulties in analysing a _____2_____ cell, some centers prefer to analyse _____9_____ cells from a late-stage _____3____.

Accepted Answer

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Question 16

Give an outline of the different laboratory approaches to testing for aneuploidies and discuss their relative merits.

Accepted Answer

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Question 17

What is involved in Southern blot hybridization?

Accepted Answer

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Question 18

Interpret the following DNA and amino acid variants:
a) g.410_411insC
b) p.Gly418*
c) c.*62A>T
d) c.142+4C>T

Accepted Answer

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Question 19

Describe the principles of arrayCGH and its applications in a diagnostic DNA laboratory.

Accepted Answer

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Question 20

The triplet repeat-primed PCR assay is commonly used in analysing samples from individuals with unstable trinucleotide repeat expansions. What is involved in this method?

Accepted Answer

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Quiz 11: Genetic Testing From Genes to Genomes, and the Ethics of Genetic Testing and Therapy