EBK BIOLOGY
4th Edition
ISBN: 8220102797376
Author: BROOKER
Publisher: YUZU
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Chapter 20.2, Problem 3CC
Summary Introduction
To determine: The information that is provided regarding gene expression if a fluorescent spot appears on a microarray.
Introduction: Genome is defined as the complete genetic material that is present in an organism. It consists of the coding as well as the non-coding parts of DNA. Genomics is the study of the genome. DNA microarray is a technique to detect the gene expression of multiple genes at the same time.
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Chapter 20 Solutions
EBK BIOLOGY
Ch. 20.1 - Prob. 1CCCh. 20.1 - Prob. 1BCCh. 20.1 - Prob. 2CCCh. 20.1 - Prob. 3CCCh. 20.1 - Prob. 4CCCh. 20.1 - Prob. 2BCCh. 20.2 - Prob. 1CCCh. 20.2 - Prob. 2CCCh. 20.2 - Prob. 3CCCh. 20.3 - Prob. 1CC
Ch. 20.3 - Prob. 2CCCh. 20.3 - Prob. 3CCCh. 20.3 - Prob. 4CCCh. 20.3 - Prob. 1EQCh. 20.3 - Prob. 2EQCh. 20.3 - Prob. 3EQCh. 20 - Prob. 1TYCh. 20 - Prob. 2TYCh. 20 - DNA ligase is needed in a cloning experiment a. to...Ch. 20 - Prob. 4TYCh. 20 - Why is Taq polymerase used in PCR rather than...Ch. 20 - Lets suppose you want to clone a gene that has...Ch. 20 - Prob. 7TYCh. 20 - Prob. 8TYCh. 20 - Prob. 9TYCh. 20 - Prob. 10TYCh. 20 - Prob. 1CQCh. 20 - Prob. 2CQCh. 20 - Prob. 3CQCh. 20 - Identify and discuss three important advances that...Ch. 20 - Prob. 2COQ
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- Both microarray and RNA-sequencing can study the transcriptomes. Compare microarray and RNA sequencing technique in analyzing gene with high, medium and low copy number of genes.arrow_forwardWithin genomics, genetic engineering and gene therapy are topics that are comparable. What do they have in common and what sets them apart?arrow_forwardExplain the concept of Functional genomics ?arrow_forward
- Need help with understanding how to set up, pick and find reading frame for doing a gene insert...arrow_forwardWithin the subject of genomics, genetic engineering and gene therapy are related. What unites them and sets them apart?arrow_forwardGive the similarities and differences of Genomics from Bioinformatics, and Proteomics from Transcriptomics and from Metabolomics.arrow_forward
- The technique of fluorescence in situ hybridization (FISH) is described. This is another method for examining sequence complexity within a genome. In this method, a DNA sequence, such as a particular gene sequence, can be detected within an intact chromosome by using a DNA probe that is complementary to the sequence.For example, let’s consider the β-globin gene, which isfound on human chromosome 11. A probe complementary to theβ-globin gene binds to that gene and shows up as a brightly colored spot on human chromosome 11. In this way, researchers can detectwhere the β-globin gene is located within a set of chromosomes. Becausethe β-globin gene is unique and because human cells are diploid(i.e., have two copies of each chromosome), a FISH experimentshows two bright spots per cell; the probe binds to each copy ofchromosome 11. What would you expect to see if you used thefollowing types of probes?A. A probe complementary to the Alu sequenceB. A probe complementary to a tandem array near…arrow_forwardExaplain the two methods to study the contents of transcriptomes which are microarray analysis and RNA sequencing. Describe the goals, methodology, and outcomes for the methods that are used.arrow_forwarda) Explain the difference between a genome and a transcriptome. Do all cells in an organism have the same genomes and or transcriptomes? b) Explain a method you could use to compare transcriptomes, and what you can learn from comparing transcriptomes.arrow_forward
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