My background is not genetics. 2.I am not interested in knowing how dna sequencing or genotyping is done. 3. I am interested just in the nature of the results as described here.
Now coming to the question: Humans have two sets of chromosome in each cell. So if I say sequencing chromosome1, what does that actually mean? Which of the two chromosome's gets sequenced? Of genotyping-do comparison take place between two+two=four chromosome1's? Or is my entire undertanding flawed?
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