
Concept explainers
To discuss:
Advantages and disadvantages of using DNA microarrays
Introduction:
A DNA microarray is a great invention as it allows for the comparison of thousands of genes at one time.The technology uses chips with attached DNA sequences as probes for gene expression. Any DNA in the sample that is complementary to a probe sequence will get bound to the chip. This technology is useful when used on known species with a sequenced genome.
The following table lists the advantages and disadvantages of using DNA microarrays.
Advantages | Disadvantages |
Provides data for thousands of genes at the same time | It is time consuming. |
Different parts of DNA can be used | It is expensive. |
Easy to store data | It has short shelf life. |
Can identify new genes | It is not good for detecting unknown microbes. |
Can study changes in the expression of proteins |
Advantages- There are several advantages of using DNA microarrays.
One DNA microarray slide can contain thousands of genes, so researchers can examine changes in the expression patterns of multiple genes at one time.
DNA microarrays can contain a few genes or all of the genes of human genome. Different parts of DNA can be used to analyze gene expression.
A large amount of information can be stored easily in one chip or one slide.
DNA microarrays help determine whether the expression of certain genes is caused by genetic factors or environmental factors. Scientists are using these to identify new genes also.
They can help in the study of changes in the expression of proteins under different growth conditions.
Disadvantages- There are some limitations in using DNA microarrays.
Real time PCR techniques are much faster than DNA microarrays to detect diseases. DNA microarrays take lot of time to analyze the chips as they are very complex.
The biggest disadvantage of DNA chips is that they are highly expensive.
DNA chips do not have a very long shelf life. So they are not very reliable.
It cannot detect unknown species so it cannot be used for unknown microbes.

Answer to Problem 28A
The following table lists the advantages and disadvantages of using DNA microarrays.
Advantages | Disadvantages |
Provides data for thousands of genes at the same time | It is time consuming. |
Different parts of DNA can be used | It is expensive. |
Easy to store data | It has short shelf life. |
Can identify new genes | It is not good for detecting unknown microbes. |
Can study changes in the expression of proteins |
Explanation of Solution
Advantages- There are several advantages of using DNA microarrays.
One DNA microarray slide can contain thousands of genes, so researchers can examine changes in the expression patterns of multiple genes at one time.
DNA microarrays can contain a few genes or all of the genes of human genome. Different parts of DNA can be used to analyze gene expression.
A large amount of information can be stored easily in one chip or one slide.
DNA microarrays help determine whether the expression of certain genes is caused by genetic factors or environmental factors. Scientists are using these to identify new genes also.
They can help in the study of changes in the expression of proteins under different growth conditions.
Disadvantages- There are some limitations in using DNA microarrays.
Real time PCR techniques are much faster than DNA microarrays to detect diseases. DNA microarrays take lot of time to analyze the chips as they are very complex.
The biggest disadvantage of DNA chips is that they are highly expensive.
DNA chips do not have a very long shelf life. So they are not very reliable.
It cannot detect unknown species so it cannot be used for unknown microbes.
Chapter 13 Solutions
Biology Illinois Edition (Glencoe Science)
Additional Science Textbook Solutions
Campbell Biology (11th Edition)
Genetic Analysis: An Integrated Approach (3rd Edition)
Chemistry & Chemical Reactivity
Applications and Investigations in Earth Science (9th Edition)
Human Anatomy & Physiology (2nd Edition)
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
- AaBbCc X AaBbCc individuals are crossed. What is the probability of their offspring having a genotype AABBCC?arrow_forwardcircle a nucleotide in the imagearrow_forward"One of the symmetry breaking events in mouse gastrulation requires the amplification of Nodal on the side of the embryo opposite to the Anterior Visceral Endoderm (AVE). Describe one way by which Nodal gets amplified in this region." My understanding of this is that there are a few ways nodal is amplified though I'm not sure if this is specifically occurs on the opposite side of the AVE. 1. pronodal cleaved by protease -> active nodal 2. Nodal -> BMP4 -> Wnt-> nodal 3. Nodal-> Nodal, Fox1 binding site 4. BMP4 on outside-> nodal Are all of these occuring opposite to AVE?arrow_forward
- If four babies are born on a given day What is the chance all four will be girls? Use genetics lawsarrow_forwardExplain each punnet square results (genotypes and probabilities)arrow_forwardGive the terminal regression line equation and R or R2 value: Give the x axis (name and units, if any) of the terminal line: Give the y axis (name and units, if any) of the terminal line: Give the first residual regression line equation and R or R2 value: Give the x axis (name and units, if any) of the first residual line : Give the y axis (name and units, if any) of the first residual line: Give the second residual regression line equation and R or R2 value: Give the x axis (name and units, if any) of the second residual line: Give the y axis (name and units, if any) of the second residual line: a) B1 Solution b) B2 c)hybrid rate constant (λ1) d)hybrid rate constant (λ2) e) ka f) t1/2,absorb g) t1/2, dist h) t1/2, elim i)apparent central compartment volume (V1,app) j) total AUC (short cut method) k) apparent volume of distribution based on AUC (VAUC,app) l)apparent clearance (CLapp) m) absolute bioavailability of oral route (need AUCiv…arrow_forward
- You inject morpholino oligonucleotides that inhibit the translation of follistatin, chordin, and noggin (FCN) at the 1 cell stage of a frog embryo. What is the effect on neurulation in the resulting embryo? Propose an experiment that would rescue an embryo injected with FCN morpholinos.arrow_forwardParticipants will be asked to create a meme regarding a topic relevant to the department of Geography, Geomatics, and Environmental Studies. Prompt: Using an online art style of your choice, please make a meme related to the study of Geography, Environment, or Geomatics.arrow_forwardPlekhg5 functions in bottle cell formation, and Shroom3 functions in neural plate closure, yet the phenotype of injecting mRNA of each into the animal pole of a fertilized egg is very similar. What is the phenotype, and why is the phenotype so similar? Is the phenotype going to be that there is a disruption of the formation of the neural tube for both of these because bottle cell formation is necessary for the neural plate to fold in forming the neural tube and Shroom3 is further needed to close the neural plate? So since both Plekhg5 and Shroom3 are used in forming the neural tube, injecting the mRNA will just lead to neural tube deformity?arrow_forward
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education





