PLoS Computational Biology · 2008 · 359 citations · 46 references
Life SciencesBioinformaticsPhylogeneticsSequence AnalysisStructural BioinformaticsHidden Markov ModelsProfile Hidden Markov ModelsSequence AlignmentLocal AlignmentLocal Alignment ScoringOptimal AlignmentProfile Hidden Markov Model AlignmentSequence Alignment UncertaintySimulation StudiesStatistical Significance Of AlignmentsStatistical Significance Testing
Sequence database searches require accurate estimation of the statistical significance of scores. Optimal local sequence alignment scores follow Gumbel distributions, but determining an important parameter of the distribution (lambda) requires time-consuming computational simulation. Moreover, optimal alignment scores are less powerful than probabilistic scores that integrate over alignment uncertainty ("Forward" scores), but the expected distribution of Forward scores remains unknown. Here, I conjecture that both expected score distributions have simple, predictable forms when full probabilistic modeling methods are used. For a probabilistic model of local sequence alignment, optimal alignment bit scores ("Viterbi" scores) are Gumbel-distributed with constant lambda = log 2, and the high scoring tail of Forward scores is exponential with the same constant lambda. Simulation studies support these conjectures over a wide range of profile/sequence comparisons, using 9,318 profile-hidden Markov models from the Pfam database. This enables efficient and accurate determination of expectation values (E-values) for both Viterbi and Forward scores for probabilistic local alignments.
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Basic local alignment search tool
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