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Pages:
11 pages/≈3025 words
Sources:
12 Sources
Style:
APA
Subject:
Technology
Type:
Term Paper
Language:
English (U.S.)
Document:
MS Word
Date:
Total cost:
$ 71.28
Topic:

Gene Editing and the CRISPR-Cas9 Technology

Term Paper Instructions:

Proposal Overview

Students must identify their topic of choice and explain it in a proposal of 250-words or less.

This proposal should include either a provisional thesis or a thesis question that the paper willanswer.

Topic selection is open, although topics must focus on an ethical issue involving the intersectionof engineering and society, preferably in the categories of safety, ecology, and sustainability.Proposals must include a reference list of at least two items.

Proposals are not assigned a grade. Rather, they will be Approved without Reservation,Approved with Reservation, or Rejected.

All students must receive approval for theirproposals before proceeding.

Term Paper Sample Content Preview:
Gene Editing
Student Name
Institutional Affiliation
Course Number and Name
Instructor’s Name
Assignment Due Date
Gene Editing
Introduction
Gene editing, also known as genome editing, is a sophisticated technique that allows scientists to change the DNA of various organisms (Chen et al.,2019). The insertion, removal, or change of genetic information at precise locations in a genome is the fundamental goal of these technologies. Genetic modification has been a topic of debate in ethical and scientific fields for many years. The CRISPR-Cas 9 technology is used to pinpoint and incorporate precise mutations into genes responsible for life-threatening illnesses. Thanks to technological advancements, scientists have modified the gene at the embryonic phase (Chen et al.,2019). When introduced into the embryos, one approach that has been studied involves a specialized enzyme compound intended to fuse specific key sections of DNA. This targeting strategy is currently considered a possible way to remove some fatal hereditary illnesses if left untreated. It has been proven to produce beneficial creatures like hornless cattle and longer-lived mushrooms. While eliminating diseases is a beautiful accomplishment, there are still several issues to be addressed, including the future extension of the genome-editing study. The Hixton Group is a team of eight nations working to promote awareness on genome editing in embryos (Chen et al.,2019). China and, more recently, the United Kingdom are the only countries that can lawfully conduct additional experimentation on this topic. States are reticent to authorize more investigation due to ethical concerns, including religious beliefs and uncertain evolutionary consequences (Doudna, 2020). Researchers can assess if gene editing on embryos should be investigated for potential use on living beings by examining scientific and ethical problems.
Background
This paper elucidates the absence of permission from the embryos used in experiments, whether the technology is sufficiently reliable and safe, whether our current knowledge of genes is sufficient to conduct clinical studies, the immature scientific technique, religion and culture, the unknown long-term impacts on people, and the possibility for misuse of the method are all contemporary ethical concerns. The paper aims to dissect the opposing perspectives toward gene editing, especially in the human body.
Research Objectives
* To determine the efficiency of gene editing in modern life.
* To determine the effectiveness of this technology towards enhancing life.
* To assess the population’s awareness of the technology.
Analysis
Reliability and safety of the technology
Gene therapy has been shown in early investigations to pose substantial health hazards, including toxicity, inflammation, and cancer. Scholars have explored the processes since and created better procedures that are less probable to cause harmful immunological responses or cancer. When gene therapy procedures are still in their infancy, specific hazards are unknown; nonetheless, medical experts, organizations, and regulatory authorities attempt to make gene therapy research, clinical trials, and authorized therapies as secure as possible.
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