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DNA-Polymerase

... of injecting DNA into agarose gel and then applying an electric current to the gel. As a result, the smaller DNA strands move faster than the larger strands through the gel toward the positive current. The size of the PCR product can be determined by comparing it with a DNA ladder, which contains DN ...
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... The Scenario begins with a grand idea of discovering the source of human variability. By the end, it gets bogged down in a technical problem, but let's leave that aside for the moment and go back to the big picture. Human variability – at least its genetic component – is the result of differences in ...
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... binding and removing repressors or binding activators to cause them to bind their activator  binding site   Corepressors:   In prokaryotes: non‐protein, small molecules that, when added turn down gene  expression either by removing activators or causing repressor to bind  In Eukaryotes: protein tha ...
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... 15. __________________________ bases form the rungs of the ladder (adenine, thymine, cytosine, guanine). 16. ____________ matches with Thymine while Cytosine matches with _____________ These are the nitrogen base pairs. 17. The order of the nitrogen bases on the DNA molecule is known as the genetic ...
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Bisulfite sequencing



Bisulphite sequencing (also known as bisulfite sequencing) is the use of bisulphite treatment of DNA to determine its pattern of methylation. DNA methylation was the first discovered epigenetic mark, and remains the most studied. In animals it predominantly involves the addition of a methyl group to the carbon-5 position of cytosine residues of the dinucleotide CpG, and is implicated in repression of transcriptional activity.Treatment of DNA with bisulphite converts cytosine residues to uracil, but leaves 5-methylcytosine residues unaffected. Thus, bisulphite treatment introduces specific changes in the DNA sequence that depend on the methylation status of individual cytosine residues, yielding single- nucleotide resolution information about the methylation status of a segment of DNA. Various analyses can be performed on the altered sequence to retrieve this information. The objective of this analysis is therefore reduced to differentiating between single nucleotide polymorphisms (cytosines and thymidine) resulting from bisulphite conversion (Figure 1).
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