Best method to determine paternity is
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Protein analysis
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Chromosome counting
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Gene counting
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DNA finger printing
About 3% or so of the human genome has highly repetitive sequences termed as simple-sequence DNA or satellite DNA that are repeated in multiples per cell and generate tandem repeats. This DNA polymorphism is revealed during DNA finger printing in the identification of paternity since it is very remote possibility to have two individuals same repeats of satellite DNA throughout the genome except they share a biological relationship. This is because a child gets half DNA from father and half from the mother. Restriction enzymes of genome produce the restriction fragments length polymorphisms, or RFLPs depending on the location of restriction sites which are then sorted by gel electrophoresis followed by southern blotting. The blots of parental and child genome are compared for sequence homology using radioactive probes; option D is correct.