CMMB 413 Lecture Notes - Lecture 13: Sanger Sequencing, Fluorophore, Meiosis

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Markers flank a gene that causes a disease. Marker 1: allele 1 linked to normal copy and 2 linked with disease. Marker 2: allele 1 also linked to normal copy and 2 is also linked with disease. As these chromosomes do meiosis, there is a chance of recombination. 5% of the time there is recombination such that allele 2 of marker 1 will travel with normal copy. No risk person is carrier for disease. Because of interference, the possibility of recombination is inhibited by such a low chance of inheriting recombination. No males because its lethal for them, need functioning proteins to survive. Sanger: design primers for dna, pcr, make many copies of region of interest. Each base is linked to a different fluorophore. Get pcr fragments of different lengths because 3"oh is changed to 3"h, therefore get smaller sizes. Smallest sequences come out first, largest ones last.

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