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How is the position of a nucleotide substitution on genome
detected? I mean that it is on exon, intron or promoter
region?
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Which of the following is not an essential condition for interference (a) The two interfering waves must be propagated in almost the same direction or the two interfering waves must intersect at a very small angle (b) The waves must have the same time period and wavelength (c) Amplitude of the two waves should be the same (d) The interfering beams of light must originate from the same source.
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Bootstrap analysis evaluates evolutionary trees by sampling columns from the original alignment with replacement (multiplying or removing some of them) and computing a proportion of times that a particular branch appears in the resulting trees. What is the main idea behind this approach?
How can we find the direction of an nucleotide substitution, for example; C to T or T to C?
Have the proteins of a family generally acquired distinctive properties within each of these three kingdoms for ancient families that arose before bacteria, archaea and eukaryotes diverged?
What is the secondary structure of intron ?
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