A probabilistic model of local sequence alignment that simplifies statistical significance estimation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 18516236.
- Also identified by DOI 10.1371/journal.pcbi.1000069 and PMC identifier 2396288.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
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.
Medical subject headings
- Algorithms
- Chromosome Mapping
- Data Interpretation, Statistical
- Models, Genetic
- Models, Statistical
- Sequence Alignment
- Sequence Analysis, DNA