Mapping equivalence for symbolic sequences: theory and applications
IEEE Transactions on Signal Processing
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Previous searches for long-range correlations in DNA sequences was carried out using statistical tools for stationary signals. However, genomic signals are non-stationary as can be attested by standard statistical tests for stationarity. In this paper, we address, in the light of non-stationary time-series analysis, the questions of (i) the existence of long-range correlations in DNA sequences and (ii) whether they are present in both coding and non-coding segments or only in the latter. It turns out that the statistical differences between coding and non-coding segments are more subtle than previously claimed by the stationary analysis. Both coding and non-coding sequences exhibit long-range correlations, as asserted by an evolutionary 1/f spectrum (i.e., having a time-dependent spectral exponent). Moreover, the average spectral exponent of non-coding segments is higher than its counterpart for coding segments. To prove that this observation is not an artifact of the 1/f evolutionary spectrum, we show, using an index of randomness that we derive from the frequency-time distribution of the genomic signals, that coding sequences are "more random" (i.e., whiter) than non-coding sequences. We believe that this result is likely the source of confusion and controversy in previous work, which relied on stationary analysis of DNA correlations.