Sanger Sequencing

Improved Essays
Abstract:
Genetic sequencing has brought about many scientific advancements, but techniques and approaches to sequencing vary, as do the goals of the sequencing. After reviewing first, second, and third-generation sequencing types, it would seem that both Sanger and Illumina-type sequencing would be most applicable to the data needed for phylogenetic systematics depending on mostly on cost and scale of research. Illumina, along with other sequencers such as those offered by 454 and nanopore, are well-suited for metagenomics and microbial studies.
Introduction
Since the discovery of the structure of DNA by Watson and Crick, DNA has become a tool by which scientists may study the genetic makeup of organisms, identifying relationships and characteristics
…show more content…
Under this method, DNA is denatured into single-strand fragments that bind to microscopic beads, and are then amplified by an oil emulsion PCR (Huse et al 2007). The beads are then placed individually in the many wells of a Picotiterplate along with sulphurylase, luciferase, and dNTPs. These reagents serve to produce a light reaction in each well that is detected by a camera and recorded into a …show more content…
Despite this, Sanger sequencing methods continue to be used for smaller-scale (and cheaper) projects and can potentially verify the results of other sequencing methods. For example, if one were to conduct a phylogenetic study on a group of eukaryotic organisms such as birds or lizards, it is often that only a few loci out of an organism’s genome actually needs to be sequenced, perhaps less than five genes. Due to its lower cost and the lack of need for high-throughput, Sanger sequencing would be the more ideal choice. In the case of larger scale projects that would require the sequencing of multiple loci and multiple species, unless the collected data has already been sequenced, Sanger sequencing would be too time-consuming and

Related Documents

  • Decent Essays

    Nt1310 Lab 6.1

    • 408 Words
    • 2 Pages

    By having a thicker gel, smaller segments can move better and not be cleared out by bigger segments. Polymerase Chain Reaction (PCR) is used to replicate DNA. In Lab 5, we created PCR amplicons by collecting our own DNA through our cheek cells, adding Taq DNA polymerase, dNTPs, primer, and a proper buffer solution into a PCR tube.…

    • 408 Words
    • 2 Pages
    Decent Essays
  • Superior Essays

    The PCR test was completed prior to the testing and was then given to each student to perform gel electrophoresis. The gel electrophoresis technique is used to separate DNA fragments and the size of the fragments determines how fast the fragments will move through the gel. This process is used to ensure that the PCR worked. To analyze the PCR, a sample mixed with the PCR and loading dye is loaded into a well in the ladder. Once the samples are loaded, the mini gel system can be turned on and begin the process of separating the DNA fragments.…

    • 1419 Words
    • 6 Pages
    Superior Essays
  • Decent Essays

    Several Advancements in technology produced a fast DNA sequencer in the 70’s, and in 1983, Karv Mullis created what is called Polymerase Chain Reaction (PCR). PCR is a very simple and inexpensive technology that is used to amplify and produce large amounts of copies of a segment of DNA. Now this has become one of the most significant scientific advances in molecular biology, PCR amplification is used every day to diagnose diseases, its also used to identify bacteria and viruses, and to match criminals to crime scenes. PCR has revolutionized the study of DNA to such an extent that Dr. Mullis was awarded the Nobel Prize in Chemistry in 1993.…

    • 110 Words
    • 1 Pages
    Decent Essays
  • Great Essays

    Oral Microbiome Essay

    • 2001 Words
    • 9 Pages

    To start these procedures a person will do a test using Colony PCR. This will be done by touching a toothpick to a selected colony and swirling with the matching 25 uL of PCR. Lastly, a person will visualize their DNA using gel electrophoresis. First, add 1.0 uL of 10X loading dye and 10uL PCR product and mix. Then Use a micropipette to load 10 uL of sample in the next open well, this will be adjacent to the preloaded DNA ladder done by the teaching assistant.…

    • 2001 Words
    • 9 Pages
    Great Essays
  • Decent Essays

    Summary: ״The CRISPR Conundrum״ “The CRISPR Conundrum” (2016) by Mary Bates, describes “CRISPR”- clustered regularly interspaced short palindromic repeats, which is a new revolutionary technology in genetic engineering. It is a kind of molecular scissors that can be programmed to snip specific bits of DNA. The article talks about the advantages of CRISPR, yet it describes CRISPR’s disadvantages as well. On the one hand, CRISPR is a cheap and precise technique to edit the DNA of animals, plants and even humans.…

    • 271 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    Although PacBio sequencing could generate much longer reads than SGS, the throughput is its weakness. There are 150,000 ZMWs on a single SMRT RSII cell, each of which could produce one polymerase read or CCS read. Typically, only 35,000~70,000 of 150,000 ZMWs on one cell could successfully produce reads due to either the failure to anchor a polymerase or loading more than one polymerase in a ZMW. Therefore, the typical throughput of the PacBio RS II system is about 0.5-1 billion bases (0.5-1 G) per SMRT cell (http://dnatech.genomecenter.ucdavis.edu/pacific-biosciences-rs/). With the advent of a new system called Sequel, the limitation to throughput has been much improved.…

    • 315 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Pacific Biosciences

    • 467 Words
    • 2 Pages

    In detection and sequence determination, the fluorescence signals for each ZMW are collected. Data is collected as a movie of the sequential signals and each individual signal is measured as a short pulse of light. Laser light travelling through the glass into the ZMW illuminates only the lower 30 nm of it since the ZMW dimensions are smaller than the wavelength of the light. This allows the selective excitation and identification of light emitted from nucleotides recruited base elongations that are being held by the polymerase for fractions of…

    • 467 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    The agarose gel is poured onto a plastic plat forming wells, and then DNA samples are placed in small wells. When samples are added to their relative wells, gel and plastic plate are…

    • 1612 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    Sanger Sequencing Report

    • 123 Words
    • 1 Pages

    Semi-automated Sanger sequencing was first described in 1977 by Sanger F. and with some improvements in the technique, remaining however conceptually unchanged it is used world-wide for clinical DNA sequencing. The method is based on the DNA polymerase-dependent synthesis of a complementary DNA strand in the presence of natural 2′-deoxynucleotides (dNTPs) and 2′,3′-dideoxynucleotides (ddNTPs) that serve as non-reversible synthesis terminators (Sanger F., 1997). The DNA synthesis reaction is randomly terminated whenever a ddNTP is added to the growing oligonucleotide chain, resulting in truncated products of varying lengths with an appropriate ddNTP at their 3′ end. The products are separated by size using polyacrylamide gel electrophoresis…

    • 123 Words
    • 1 Pages
    Improved Essays
  • Improved Essays

    Sequencing Essay

    • 1108 Words
    • 5 Pages

    Sequencing the human genome has been a huge scientific project for decades now. Scientists everywhere have been racing to see who can sequence the human genome first. Craig Venter, an intensely…

    • 1108 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Dna Profile Case Study

    • 696 Words
    • 3 Pages

    I feel better informed to answer the question of whether I would want to obtain my DNA profile after researching this subject more thoroughly. With the little I knew before researching this subject I would be inclined to say that I would want my DNA profile especially now that the market prices for these services seems to be decreasing since first made available to the public. I am also going to go out on a limb here and say that it is probably pretty accurate to assume that the average person also lacks understanding of all the intricacies that go along with having their DNA profile data made known. Sure it is nice to have this type of information in order to learn what common diseases and conditions we are vulnerable too such as those in particular that tend to go undiagnosed for a while yet can reap so much damage if not diagnosed early on. The three most common that come to mind are Diabetes, High Blood Pressure and Cancer.…

    • 696 Words
    • 3 Pages
    Improved Essays
  • Great Essays

    If you had told someone in the early 1800’s that every cell in your body contains something called DNA made of molecules called nucleotides (DNA) that determine every characteristic about you, from your height and eye color to whether or not you’ll get a certain disease or condition, they would think you were crazy. Today, most students learn about DNA in middle school biology. DNA was first discovered by a German biochemist named Frederich Miescher in 1869, but its importance was not realized until 1953 (DNA). Genetic testing, “a type of medical test that identifies changes in chromosomes, genes, or proteins” (What is Genetic Testing?), however, was first done in the 1910s with ABO blood typing (O’Neil). Today, testing is used for determining paternity, determining a person’s chance of developing or passing on a genetic disorder, and to confirm or rule out a suspected genetic condition (What is genetic testing?).…

    • 1404 Words
    • 6 Pages
    Great Essays
  • Great Essays

    Mitochondrial DNA has many beneficial uses for DNA sequencing such as; its ability to be extracted from small…

    • 1855 Words
    • 8 Pages
    Great Essays
  • Improved Essays

    Some scientists think that exome sequencing is more beneficial than WGS because we only know how to interpret the exon of the genome (Perkel, 2013, p. 262). Although WGS produces more data (including the noncoding regions) this alone does not outweigh the fact that it is more expensive and provides results at a slower rate than exome…

    • 1740 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    Unit 18 - Genetics (Assignment 1) Task 1. Deoxyribonucleic acid (DNA for short) is genetic material that carry’s the majority of information for development growth and many other functions. DNA is located in the nucleus of a cell. DNA has a double helix structure and is formed by a series of bases these are Adenine , Cytosine , Guanine and Thymine.…

    • 782 Words
    • 4 Pages
    Improved Essays

Related Topics