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    sequencer is based on the electrical characterization of individual nucleobases‚ while DNA passes through a nanopore with integrated nanotube side electrodes. (7) “$1000 per genome” low cost sequencing for the entire human genome by 2014 (8) Cost $3 billion to sequence 3 billion‚ now less than $100‚000 per human genome‚ future $1000 Genome (6) First convert the DNA to an expanded‚ digitized form by systematically substituting each and every base in the DNA sequence with a specific ordered pair of concatenated

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    Biochemistry Task 1 Essay

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    (Medical Institution‚ 2016) References National Human Genome Research Institute (2015‚ June 16). Deoxyribonucleic Acid. Retrieved September 4‚ 2016‚ from National Human Genome Research Institute‚ https://www.genome.gov/25520880/deoxyribonucleic-acid-dna-fact-sheet/ (National Human Genome Research Institute‚ 2016) What is DNA replication (2016). Retrieved September 4‚ 2016‚ from http://www.yourgenome.org/facts/what-is-dna-replication (Your Genome‚ 2016)

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    FISH FISH stands for Fluorescence in situ hybridization. FISH is a technique in the lab used to see where a DNA sequence or certain gene is located in an individual’s genome. This allows scientists to look for genetic conditions caused by alterations in chromosomes. FISH can be used to find distinct features in DNA for genetic counseling‚ species identification‚ and medicine. It can also be used to find certain RNA points in cells and tissue samples. FISH is used on blood samples or any other cell

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    Dna Sequencing

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    research and discovery. The rapid speed of sequencing attained with modern DNA sequencing technology has been instrumental in the sequencing of thehuman genome‚ in the Human Genome Project. Related projects‚ often by scientific collaboration across continents‚ have generated the complete DNA sequences of many animal‚ plant‚ and microbial genomes. The first DNA sequences were obtained in the early 1970s by academic researchers using laborious methods based on two-dimensional chromatography. Following

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    Mitochondrial Dna

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    specific DNA to be helpful in determining lineage. Within the mitochondria‚ numerous copies of DNA are found. The mitochondrial DNA is therefore more practical to use than the one copy in the traditional nucleus. The mitochondria itself has it’s own genome and has its own genes. The tiny organelle has a mere 37 genes that mainly remain unchanged (Rice University). According to Genebase‚ the mtDNA is also much smaller than nucleic DNA. Nucleic DNA ranges from 49‚530‚000 to 247‚200‚000 base pairs the

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    Vaccinations that act through different mechanisms provide methods of best containing viral spread. The significance that comes with vaccinations is understanding the herd mentality that medicine follows. In order to best protect a large population‚ it is not necessary‚ and is nearly impossible‚ to vaccinate all members of that community. However‚ vaccinations still prove to be effective methods of preventing diseases. This occurs by ensuring that an infected person is most likely to come into contact

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    of the cell-free DNA floating in a pregnant woman’s blood stream stems from her fetus. In 2010 in a paper published in Science Translational Medicine‚ Lo’s group showed that enough fragments of fetal DNA are there to reconstruct the fetus’s whole genome‚ and it should be possible to use this DNA to test the unborn child for genetic diseases without exposing it to the risk of an invasive procedure. One strategy makes use of subtle genetic variations that exist between a mother’s pairs of chromosomes

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    AP Bio Ch. 20 Vocabulary

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    its location to be detected. 10. Complementary DNA (cDNA) – A DNA molecule made in vitro using mRNA as a template and the enzyme reverse transcriptase. A cDNA molecule therefore corresponds to a gene‚ but lacks the introns present in the DNA of the genome. 11. Polymerase Chain Reaction (PCR) – A technique for amplifying DNA in vitro by incubating with special primers‚ DNA polymerase molecules‚ and nucleotides. 12. Gel Electrophoresis – The separation of nucleic acids or proteins‚ on the basis of

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    Systems Microbiology

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    Systems Biology Systems biology involves the study of an organism as one single system. Instead of analysing all the individual components that make up a cell‚ the cell is instead viewed as an interacting network of genes‚ proteins and biochemical reactions and these are studied as a whole. In 20th century‚ molecular biology was focused upon. A ‘reductionist’ approach was followed‚ in which the individual components‚ such as the cell nucleus or sugar metabolism‚ were studied in isolation. However

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    Human Geome Project

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    everything else constant | * Accuracy | How accurate results are | * Dependent variable | Relies on independent variable‚ plotted on y-axis | * Independent variable | One you change‚ plotted on x-axis | What is the Human Genome? The human genome comprises a sequence of approximately 3 billion component parts‚ called nucleotides‚ which are organized into DNA molecules—the double helix. The nucleotides‚ which serve as the alphabet for the language of life‚ are represented by just four

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