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Mutations
Mutations

... Suggests that variation in evolutionary rates is greater than that observed by chance alone: – Mutation rates vary greatly among different evolutionary lineages – Changes in functional constraint and selection: accelerated rates of evolution in insulin in some rodents due to adaptive changes – Subst ...
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waardenburg syndrome, type iv

... Expansion of trinucleotide repeats can give rise to genetic disease. We have developed a technique, repeat expansion detection (RED), that can identify potentially pathological repeat expansion without prior knowledge of chromosomal location. Human genomic DNA is used as a template for a two-step cy ...
Decoding the Language of Genetics
Decoding the Language of Genetics

... diverse, differing in such basic things as the number of copies of their genome their cells normally contain. The analytical ideas emphasized here apply to every organism, even though not every kind of experiment is possible in all of them. Specifically, some organisms (viruses, bacteria, plants, an ...
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... Whenever cells replicate there is a chance for a copying error. When DNA is exposed to mutagens, there is the chance for a mutation. Over time mutations change the genetic code; if they change the phenotype of the individual in a way that makes them more fit to survive, the mutations will persist. I ...
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... mutations in the LacZ gene are white. By screening many colonies on such plates it is possible to isolate a collection of E. coli mutants with alterations in the LacZ gene. PCR amplification of the LacZ gene from each mutant followed by DNA sequencing allows the base changes that cause the LacZ– phe ...
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... capillary electrophoresis device. To assess potential differences between measurements by the instruments used, ten centrally prepared PCR products were distributed and analyzed on each type of apparatus. The tests were performed in duplicate and the differences observed were subjected to statistica ...
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... The process of making the protein from the instructions on the mRNA Occurs in the ribosomes Codon – a sequence of 3 bases that codes for a specific amino acid Anticodon – the complementary 3 base sequence on a tRNA molecule ...
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... Molecular biology techniques such as DNA sequencing are important tools for enforcing laws that protect threatened or endangered species. Just as human tissue collected at a crime scene can yield DNA profiles that can be used to identify victims and suspects, unidentifiable animal tissues such as dr ...
Emerging Trends in Computational Biology, Bioinformatics, and
Emerging Trends in Computational Biology, Bioinformatics, and

... it necessarily has the same base sequence in the same 5’➔3’ direction as the DNA strand complementary to the template strand, except for the substitution of U for T. This DNA strand, designated the sense strand, may therefore be read directly from the genetic code table, substituting T for U. As a b ...
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PCR of GFP - the BIOTECH Project
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... Topoisomerase II - cleaves both strands, allows unwinding of the overwound Watson and Crick strands (an energy-requiring process) and rejoins the ends. Uses ATP as a co-factor. A version of this enzyme in bacteria is called "gyrase." Gyrase makes a double strand scission, forcibly underwinds the DNA ...
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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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