FASTA (Fast Alignment and Search Tool) is a widely used bioinformatics algorithm and format for sequence similarity searching and sequence database indexing. It was developed by William R. Pearson and David J. Lipman in the early 1980s. The FASTA algorithm is designed to quickly search for regions of local similarity between a query sequence and a sequence database by utilizing efficient indexing techniques and scoring methods.
The following features of the FASTA algorithm:
- Indexing the Sequence Database:
- The first step in the FASTA algorithm involves indexing the sequences in the database. This is typically done using a data structure called a “seed index” or a “lookup table.” The seed index is constructed by selecting short words (typically 2-4 residues in length) from each sequence in the database and storing their positions in the index.
- The seed index allows for rapid identification of potential matches between the query sequence and the database sequences. The selected word length determines the sensitivity and speed of the search; longer words provide higher specificity but slower search times.
- Scoring the Sequence Similarity:
- The FASTA algorithm utilizes a scoring system to evaluate the similarity between the query sequence and each database sequence. The scoring system assigns scores based on the degree of similarity between aligned residues.
- In the original FASTA algorithm, the scoring is performed using a substitution matrix, such as the PAM or BLOSUM matrix, which quantifies the likelihood of amino acid substitutions based on evolutionary observations. The scoring can also be performed using simpler methods, such as assigning fixed scores for match and mismatch or using a scoring scheme based on sequence identities and conservative substitutions.
- The scoring system considers various factors, including the match score, mismatch penalty, gap penalties, and scoring matrices, to compute an alignment score that reflects the similarity between the sequences.
- Identifying Regions of Local Similarity:
- The core of the FASTA algorithm involves identifying regions of local similarity between the query sequence and the database sequences.
- The algorithm starts by selecting a word (seed) from the query sequence and searching the seed index to find potential matches in the database sequences.
- Once a potential match is found, the algorithm extends the alignment in both directions, gradually building the alignment and updating the alignment score.
- The alignment extension continues until the alignment score drops below a specified threshold or reaches a predefined alignment length.
- The algorithm applies heuristics to optimize the search and prioritize high-scoring regions.
- Statistical Significance Estimation:
- After identifying regions of local similarity, the FASTA algorithm assesses the statistical significance of the alignments to determine if they are significant by chance or likely to be biologically meaningful.
- The algorithm calculates a statistical score, known as the “E-value,” which estimates the expected number of alignments with a score equal to or better than the observed alignment score.
- The E-value is computed based on the database size, the scoring system used, and the alignment score. A lower E-value indicates a higher statistical significance and suggests a more meaningful biological relationship between the sequences.
- Reporting Results:
- Finally, the FASTA algorithm generates a report that includes the identified alignments, their alignment scores, E-values, and other relevant information.
- The report lists the database sequences that show significant similarity to the query sequence, allowing researchers to further analyze and interpret the results.
The FASTA algorithm utilizes efficient indexing techniques, scoring systems, and statistical significance estimation to quickly identify regions of local similarity between a query sequence and a sequence database. It is a widely used tool for sequence similarity searching and has been instrumental in numerous bioinformatics applications, including protein and nucleotide sequence analysis, homology detection, and functional annotation.
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