Biology: The Dynamic Science (MindTap Course List)
Biology: The Dynamic Science (MindTap Course List)
4th Edition
ISBN: 9781305389892
Author: Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher: Cengage Learning
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 19, Problem 1TYK
Summary Introduction

Introduction:

The process of determining the sequence of nucleic acid is known as DNA (deoxyribonucleic acid) sequencing. There are several methods to sequence the DNA such as the Sanger method, which is also known as the dideoxy sequencing, and modern third generation methods such as Solexa/Illumina DNA sequencing method.

Expert Solution & Answer
Check Mark

Answer to Problem 1TYK

Correct answer:

The sequencing of DNA fragments is more at the same time.

Explanation of Solution

Explanation for the correct answer:

Option (b) states that the Illumina DNA sequencing method sequences more DNA fragments at the same time. The Illumina method is the NGS (next-generation sequencing) technique. This technique involves the sequencing of DNA by tracking the nucleotides that are labeled as the copies of DNA. This takes place in a parallel fashion. The data output in illumina method is up to 300 kb (kilobases) to several tb (terabases) just in a single run as compared to Sanger method, which requires large amount of DNA for each read. Hence, option (b) is correct.

Explanation for the incorrect answer:

Option (a) states that the sequencing of longer fragments of DNA takes place in the Illumina DNA sequencing method. The DNA fragments are cut short during the sequencing of DNA using the Illumina method. These short double-stranded adapter molecules are attached to the end of the DNA fragments with the help of an enzyme known as DNA ligase. So, it is an incorrect option.

Option (c) states that the fluorescent markers are not required. Illumina sequencing of DNA involves the addition of primer to the cell. This primer attaches to each DNA strand and then DNA is synthesized. The synthesis of each DNA strand is done with the help of four different fluorescent labels put on the DNA nucleotide progenitor. So, it is an incorrect option.

Option (d) is states that the amplification of DNA is not done before sequencing. DNA strands form a cluster of multiple copies of DNA during the sequencing by the Illumina DNA sequencing method that is single-stranded. This single-stranded DNA undergoes the process of amplification. So, it is an incorrect option.

Option (e) states that the computer algorithms are not required to look for places where overlapping of sequencing takes place. The fluorescent tagging on nucleotides enables computer to analyze the kind of base that was added with the help of the wavelength. The computer remembers it for every spot and the molecules that are not corporated are removed. So, it is an incorrect option.

Hence, options (a), (c), (d), and (e) are incorrect.

Conclusion

Therefore, it may be concluded that the Illumina DNA sequencing method is faster as it only requires a single strand of DNA while Sanger method requires multiple copies of DNA. The Illumina DNA sequencing method can sequence a number of DNA fragments at the same time.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
In next-generation sequencing, which of these advances allows for massively parallel sequencing?       a.  Pieces of DNA are fixed to a surface, so we can tell which new nucleotides were added to each piece.       b.  DNA sequences are read in real-time as nucleotides are added to each piece.       c.  Each segment of the genome can be pieced back together through shotgun alignment       d.  Single molecules of DNA can be read without the need for amplification.
Would it be possible to use human polymerase for the PCR reaction? a. No, because human polymerase does not have the ability to withstand the high temperatures required for the PCR reaction to occur. b. No, because human polymerase cannot be extracted from cells to use in a lab setting.  c. Yes, because we are using human DNA as the template DNA. d. Yes, because human polymerase can add bases to a template strand without a primer.
(A) After three cycles of PCR, how many DNA molecules are present that correspond precisely to the desired amplification product? (B) What about after 5 cycles. Assume that we started with one molecule in each case, and that the reaction is perfectly efficient.
Knowledge Booster
Background pattern image
Biology
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Biology: The Dynamic Science (MindTap Course List)
Biology
ISBN:9781305389892
Author:Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher:Cengage Learning
Text book image
Concepts of Biology
Biology
ISBN:9781938168116
Author:Samantha Fowler, Rebecca Roush, James Wise
Publisher:OpenStax College
Text book image
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning
Molecular Techniques: Basic Concepts; Author: Dr. A's Clinical Lab Videos;https://www.youtube.com/watch?v=7HFHZy8h6z0;License: Standard Youtube License