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📄 codcmp.txt

📁 emboss的linux版本的源代码
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                                  codcmp Function   Codon usage table comparisonDescription   This program reads in two codon usage table files.   It counts the number of the 64 possible codons which are unused (i.e.   has a usage fraction of 0) in either one or the other or both of the   codon usage tables.   The usage fraction of a codon is its proportion (0 to 1) of the total   of the codons in the sequences used to construct the usage table.   For each codon that is used in both tables, it takes the difference   between the usage fraction. The sum of the differences and the sum of   the differences squared is reported in the output file, together with   the number of unused codons.  Statistical significance   Question:   How do you interpret the statistical significance of any difference   between the tables?   Answer:   This is a very interesting question. I don't think that there is any   way to say if it is statistically significant just from looking at it,   as it is essentially a descriptive statistic about the difference   between two 64-mer vectors. If you have a whole lot of sequences and   codcmp results for all the possible pairwise comparisons, then the   resulting distance matrix can be used to build a phylogenetic tree   based on codon usage.   However, if you generate a series of random sequences, measure their   codon usage and then do codcmp between each of your test sequences and   all the random sequences, you could then use a z-test to see if the   result between the two test sequences was outside of the top or bottom   5%.   This would assume that the codcmp results were normally distributed,   but you could test that too. The simplest way is just to plot them and   look for a bell-curve. For more rigour, find the mean and standard   deviation of your results from the random sequences, use the normal   distribution equation to generate a theoretical distribution for that   mean and standard deviation, and then perform a chi square between the   random data and the theoretically generated normal distribution. If   you generate two sets of random data, each based on your two test   sequences, an F-test should be used to establish that they have equal   variances. Then you can safely go ahead and perform the z-test.   You could use shuffle to base your random sequences on the test   sequences - so that would ensure the randomised background had the   same nucleotide content.   F-tests, z-tests and chi-tests can all be done in Excel, as well as   being standard in most statistical analysis packages.   Answered by Derek Gatherer <d.gatherer 

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