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Basic Python
Basic Python

... interpreter executes each statement one at a time. • No compilation or linking is required. • Python programs are called scripts which are simple text files. To execute a script we pass it through the interpreter. ...
DNA
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... B. How does DNA fit in the cell? 1. Think about it! The DNA strand can be incredibly LONG! Human DNA molecules contain up to 4,639,221,000 base pairs. That means there is about 1-2 meters of DNA in each cell. How can it be kept in such a small area? ...
Supplementary information - Springer Static Content Server
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... Kit (Illumina Inc.). Briefly, 100 ng of genomic DNA was diluted in 52.5 µl TE buffer and fragmented in Covaris Crimp Cap microtubes on a Covaris E220 ultrasonicator (Woburn). According to Illumina’s recommendations for a 350-bp average fragment size, the settings used were 5% duty factor, 175 W peak ...
Nucleic acids
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... can form with A. Each base can form either two or three hydrogen bonds in a matched pair. The AT pair forms two, and the GC pair, three. However, when C is lined up against A, no hydrogen bonds can be formed (because donors do not line up with acceptors ...
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... Purpose of DNA DNA is one of “THE BIG FOUR” Organic Macromolecules (a Nucleic Acid) Deoxyribonucleic Acid Why do we have DNA? It is our genetic information • The “code” for all of our ...
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2013 - (canvas.brown.edu).
2013 - (canvas.brown.edu).

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Timeline of Genetics - Bioinformatics Software and Tools
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Nucleic Acids - Cochise College
Nucleic Acids - Cochise College

... • a section of DNA containing the gene unwinds. • one strand of DNA bases is used as a template. • mRNA is synthesized using complementary base pairing with uracil (U) replacing thymine (T). • the newly formed mRNA moves out of the nucleus to ribosomes in the cytoplasm. ...
FREE Sample Here
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DNA replication, transcription & translation
DNA replication, transcription & translation

... 1. Helicase enzyme breaks the hydrogen bonds between base pairs. This unzips the double helix at a position called the replication fork. 2. There is an abundant supply of nucleotides in the nucleus for the formation of the new polynucleotides. 3. Nucleotides base pair to the bases in the original st ...
Genes and Chromosomes
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... DNA is usually between genes, but not always. Some regions of repeated sequence have a special function; see telomeres and centromeres below. The majority of repetitive sequence has no known function. The unit of repeated sequence can range from a single nucleotide to several 100 nucleotides. Region ...
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Interpretation of Complex Forensic DNA Mixtures
Interpretation of Complex Forensic DNA Mixtures

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The Nobel Prize in Medicine
The Nobel Prize in Medicine

... UCU) produced two alternating amino acids. This, combined with the Nirenberg and Leder experiment, showed that UCU codes for Serine and CUC codes for Leucine. ...
recombinant dna technology and genetic engineering
recombinant dna technology and genetic engineering

... with a fluorescent label, the temperature is lowered so it has time to incorporate the 'strange' molecules10, 11. Mechanism of extension: The primers, where there are a few bases built in, already have a stronger ionic attraction to the template than the forces breaking these attractions. Primers th ...
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Microsatellite



A microsatellite is a tract of repetitive DNA in which certain DNA motifs (ranging in length from 2–5 base pairs) are repeated, typically 5-50 times. Microsatellites occur at thousands of locations in the human genome and they are notable for their high mutation rate and high diversity in the population. Microsatellites and their longer cousins, the minisatellites, together are classified as VNTR (variable number of tandem repeats) DNA. The name ""satellite"" refers to the early observation that centrifugation of genomic DNA in a test tube separates a prominent layer of bulk DNA from accompanying ""satellite"" layers of repetitive DNA. Microsatellites are often referred to as short tandem repeats (STRs) by forensic geneticists, or as simple sequence repeats (SSRs) by plant geneticists.They are widely used for DNA profiling in kinship analysis and in forensic identification. They are also used in genetic linkage analysis/marker assisted selection to locate a gene or a mutation responsible for a given trait or disease.
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