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Green, Ed, NEADERTHAL DNA, UC Santa Cruz, June
Green, Ed, NEADERTHAL DNA, UC Santa Cruz, June

... one set of dna from mom and one set from dad... that is what DIPLOID means. where in that genome are these uniquely human characteristictics encoded... what makes humans unique genetically?. 35M SNP changes (single nucleotide polymorphisms.) 5M insertion/deletions 9 pericentric inversions and 1 chro ...
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... a. The DNA produced came out as lots of short sections of DNA, a few hundred base-pairs long, rather than one continuous strand. ...
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...  Know what linkage is. How is the behavior of linked genes during meiosis different from genes that Mendel studied? Which one of Mendel’s laws does not apply when two genes are linked?  How is genetic distance between two genes located on the same chromosome calculated using linkage? Who discovere ...
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PowerPoint - Biological Sciences

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... interact with the DNA. SASA values are re-calculated with the DNA present to determine the complex SASA (SASAC). The BASA of each residue is defined as BASA = SASAF – SASAC, which will always be greater than or equal to zero. Residues with BASA > 0 are considered to be in contact with the DNA, and ...
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DNA

...  Large numbers of copies of specific DNA sequences can be amplified simultaneously with multiplex PCR reactions.  Commercial kits are now available for easy PCR reaction setup and amplification. Problem: Contaminant DNA, such as fungal and bacterial sources, will not amplify because human-specific ...
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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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