Efficient (linear time) algorithms are described for identifying global molecular sequence features allowing for errors including repeats, matches between sequences, dyad symmetry pairings, and other sequence patterns. A multiple sequence alignment algorithm is also described. Specific applications are given to hepatitis B viruses and the J5-C (J, joining; C, constant) region of the immunoglobulin kappa gene.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC279651 | PMC |
http://dx.doi.org/10.1073/pnas.85.3.841 | DOI Listing |
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