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Disadvantages of human genome project
The importance of the human genome project
Use of DNA in criminal investigations
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DNA sequencing
Definition
DNA sequencing is the process of determining the precise order of nucleotide within a DNA molecules. It include any method or technology that order of the four bases – adenine, guanine, cytosine and thymine in a strand of DNA.
Or “ The process of determining the order of bases in given DNA strand.
What can the DNA sequence tell us?
• Predict the sequence of amino acids of proteins encoded by the DNA
• Determines the composition of RNA molecules encoded by the DNA e.g., rRNA, tRNA
• Locate the position and determine the composition of introns in gene from eukaryotes
• Characterize the complete genetic make-up of an organism (Genome Sequencing)
There are main three methods for detecting DNA sequence
Use of Sequencing
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Human genome project is the biggest example of DNA sequencing. When the human genome was sequenced back in 2001, many issue rose but now after many year, we can see its impacts on medical and pharmaceutical research. Scientists are now able to identify the genes which are responsible for causing genetic diseases like Alzheimer's disease, Cystic fibrosis, myotonic dystrophy and many other diseases caused by the disability of genes to function properly. Many types of acquired diseases like cancers can also be detected by observing certain genes.
Use of Sequencing
DNA sequencing may be used to determine the sequence of individual genes, larger genetic regions (i.e. clusters of genes or operons), full chromosomes or entire genomes. Sequencing provides the order of individual nucleotides present in molecules of DNA or RNA isolated from animals, plants, bacteria, archaea, or virtually any other source of genetic information. This information is useful to various fields of biology and other sciences, medicine, forensics, and other areas of study.
Molecular
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This is a form of genetic testing, though some genetic tests may not involve DNA sequencing. In medical research, DNA sequencing can be used to detect the genes which are associated with some heredity or acquired diseases. Scientists use different techniques of genetic engineering like gene therapy to identify the defected genes and replace them with the healthy ones.
Forensics
DNA sequencing may be used along with DNA profiling methods for forensic identification and paternity testing. DNA sequencing has been applied in forensics science to identify particular individual because every individual has unique sequence of his/her DNA. It is particularly used to identify the criminals by finding some proof from the crime scene in the form of hair, nail, skin or blood samples. DNA sequencing is also used to determine the paternity of the child. Similarly, it also identifies the endangered and protected species.
It helps medics to find a direct genetic cause of the patient’s condition and target it with pharmaceutical or other therapies. The technology is used for the identification of DNA sequences that increase risks of current diseases and disorders; with this information carriers can start to make efforts to prevent them before the development of the problem. The video mentioned 200 actionable genes, structures that have direct links with a specific condition. Knowing about their presence, people have a chance to bring in preventive measures like taking anticoagulants in the case of identification of a thrombogenic gene. The technology led to the significant improvement of diagnostics and personalized treatments. It helped to find a rare, life-threatening mutation in case of Beery twins and assign a drug to a girl (Alexis) that returned her to a normal life. In the case of cancer genome sequencing led to the development of genetic drags, which target essential tumor genes and make malign structures to shrink. The video mentioned a product that works with the BRАF protein that induces cells to uncontrolled division; the drug led to the remission in the patient with metastasizing melanoma. Such treatment was effective in the case of cystic fibrosis. In the case of the breast cancer the technology helps to evaluate the aggressiveness of the condition and make a personalized decision about chemotherapy. The video also mentioned the pre-implantation genetic diagnosis – an early-staged technology that prevents the development of inherited disorders in
Deoxyribonucleic acid (DNA) is an acclaimed extraordinary discovery that has contributed great benefits in several fields throughout the world. DNA evidence is accounted for in the majority of cases presented in the criminal justice system. It is known as our very own unique genetic fingerprint; “a chromosome molecule which carries genetic coding unique to each person with the only exception of identical twins (that is why it is also called 'DNA fingerprinting ')” (Duhaime, n.d.). DNA is found in the nuclei of cells of nearly all living things.
. DNA can be left or collected from the hair, saliva, blood, mucus, semen, urine, fecal matter, and even the bones. DNA analysis has been the most recent technique employed by the forensic science community to identify a suspect or victim since the use of fingerprinting. Moreover, since the introduction of this new technique, there has been a large number of individuals released or convicted of crimes based on DNA left at the crime scene. DNA is the abbreviation for deoxyribonucleic acid.
Many things have impacted both the Science and Medical fields of study. Electrophoresis and DNA Sequencing are two of these things. Together they have simultaneously impacted both of these fields. On one hand, there is Electrophoresis. Electrophoresis is a specific method of separating molecules by their size through the application of an electric field. It causes molecules to migrate at a rate and distance dependent on their size. On the other hand, there is DNA Sequencing. DNA Sequencing is a technique used to determine the exact sequence of bases
Gene mapping is currently being used to identify genes that can put people at risk for illness and to help the development of new medicines. Scientists hope to use gene mapping to lead to advancement in medicines, the treatment to disease, and its aid in disease prevention. Genetic mapping was the initial step in the Human Genome Project (human genome project). The Human Genome Project identified thousands of DNA sequences and located important standards they called landmarks. Scientist use these landmarks to tell them where each fragment of DNA came from. These maps would be used to locate sick genes, diseases, or abnormal genes (genome.gov).
Forensics has been greatly enhanced by technology. DNA profiling is one of the technologies that has influenced efficiency and credibility of forensic evidence. The FBI first started using DNA in one of its cases in 1988. In Europe, the United Kingdom opened a DNA database in 1955 (Milena, 2006). The main use of the DNA is to compare the evidence collected at crime scene with the suspects. In addition, it helps to establish a connection between the evidence and the criminals. The investigations have been simplified through the use of technology and DNA has been one of the most effective methods in investigations.
DNA analysis is a scientific process among the newest and most sophisicated of techniques used to test for genetic disorders, which involves direct examination of the DNA molecule itself (Lyman, 2014) . Today crime labs use mtDNA analysis. This type of analysis allows smaller degraded pieces of DNA to still be successfully tested (Lyman, 2014) . There are several steps taken when analyzing DNA in forensics. When testing scientists must first isolate the DNA so it is not contaminated and can't be used. Lab technicians the take small pieces of the DNA, conserving as much as they can encase they need to test again. Once testing is done the next step is determining the DNA test results and finally there is the comparison and interpretation of the test results from the unknown and known samples to determ...
Once the project began in 1990, fewer than one hundred human sickness genes had been known. At the project 's conclusion in 2003, the quantity of known sickness genes had up to over fourteen-hundred, however, the human order project centered on the polymer sequence of a personal. The results of human genome project results in significant improvement of the medicines for different diseases. The project initiated by the government enables the researchers and the doctors to understand the etiology of less known disease. After knowing the factors behind the disease, researchers tried to find out the medicines which could treat those diseases and diminish their effects. It also made the world aware of the fact that genes could be used for the research and medical purposes in the field of medicine. As a result of this project, it became very easy to produce the clones and the genes by performing the gene sequencing and different analysis on the genes of a person. The future of this project, doctors will become completely able to understand the hidden causes of the disease which will later on help in understanding the management of their
By reading the DNA of a fetus Prenatal DNA sequencing is the next dividing line of the genome revolution. Prenatal DNA sequencing is a noninvasive screening in which scientist can be able to sequence the DNA before birth. This is a primary process of gene altering in which where researchers are trying to correct an imperfection in a child. Scientist has discovered by a mother giving her blood sample and the father giving a spit sample, an entire genome of their fetus can be born. Clinical test capitalize on this DNA to discern the baby’s sex and determine whether mother and child have incompatible Rh blood groups, which can lead to fatal complications. Every gene and every chromosome known about a baby’s genetic make-up, while still in the u...
Once a crime has been committed the most important item to recover is any type of evidence left at the scene. If the suspect left any Deoxyribonucleic acid (DNA) at the crime scene, he could then be linked to the crime and eventually charged. A suspect’s DNA can be recovered if the suspect leaves a sample of his or her DNA at the crime scene. However, this method was not always used to track down a suspect. Not too long ago, detectives used to use bite marks, blood stain detection, blood grouping as the primary tool to identify a suspect. DNA can be left or collected from the hair, saliva, blood, mucus, semen, urine, fecal matter, and even the bones. DNA analysis has been the most recent technique employed by the forensic science community to identify a suspect or victim since the use of fingerprinting. Moreover, since the introduction of this new technique it has been a la...
Unsolved cold cases such as murder and rapes, allow violent offenders to remain in society. Often times at crime scenes, the offender has deposited some biological evidence within the scene. At all crime scenes, the most reliable evidence tying an offender to the scene is physical evidence, such as biological material, skin, hair, blood and other bodily fluids. This biological evidence left behind by the offender is the key piece of evidence to identify and apprehend an offender. Prior to the advancements in DNA identification technology and databases, cases of murder and rape remained opened and unsolved due to biological evidence was unable to be processed for a DNA profile. In the mid-1980s, DNA testing emerged as a crucial process in determining a genetic profile of biological materials found at crime scenes. The genetic profile could then be compared to known persons to confirm or eliminate the person as an
In this field, specialists go through thorough efforts to determine the entire DNA sequence of an organism and map out its genetics. With this information, scientists are able to study the genes that are involved in diseases like cancer, diabetes and heart diseases and possibly find a way to alter them so that those types of serious diseases may be avoidable for future generations. Fred Sanger was the first man to originate Genomics. When he sequenced the genomes of a virus and of a mitochondrial, he and his group established different genomic techniques for sequencing between 1970 and 1980. From 1970 until now Genomics has grown into The Genomic Science Programme, which falls under The Human Genome Project and is led by the National Human Genome Research Institute in America.
Genetic testing is the process of sequencing six billion letters of a human genome to possibly discover genetic differences, such as how cells carry the same genome but at the same time look and function different. Genetic testing is also the process that can give foresight into pathological diseases such as different types of cancer.
This shape looks much like a twisted ladder and gives the DNA the power to pass along biological instructions with great precision. The scientific and medical progress of DNA has been immense, from involving the identification of our genes that trigger major diseases or the creation and manufacture of drugs to treat these diseases. DNA has many significant uses in society, health and culture today. One important area of DNA research is that used for genetic and medical research. Our ability to now diagnose a disease in its earlier stages has been greatly improved....
For example such as medicine, it can be sometime possible to reading DNA sequences and find out how some diseases occur. It can sometimes be possible to fight some infectious diseases or any form of disease by changing the DNA codons which cause most of these problems.