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FASTA is a DNA and Protein sequence alignment software package first described (as FASTP) by David J. Lipman and William R. Pearson in 1985 in the article Rapid and sensitive protein similarity searches. The original FASTP program was designed for protein sequence similarity searching. FASTA, described in 1988(Improved Programs for Biological Sequence Comparison) added the ability to do DNA:DNA searches, translated protein:DNA searches and provided a more sophisticated shuffling program for evaluating statistical significance. There are several programs in this package that allow the alignment of protein sequences and DNA sequences. FASTA is pronounced "FAST-Aye", and stands for "FAST-All", because it works with any alphabet, an extension of "FAST-P" (protein) and "FAST-N" (nucleotide) alignment. Software development is the translation of a user need or marketing goal into a software product. ...
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Linux, or GNU/Linux, refers to any Unix-like computer operating system which uses the Linux kernel. ...
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The structure of part of a DNA double helix. ...
A representation of the 3D structure of myoglobin, showing coloured alpha helices. ...
In bioinformatics, a sequence alignment is a way of arranging the primary sequences of DNA, RNA, or protein to identify regions of similarity that may be a consequence of functional, structural, or evolutionary relationships between the sequences. ...
David J. Lipman is an American biologist who since 1989 has been the Director of NCBI (the National Center for Biotechnology Information) at the National Institutes of Health. ...
A representation of the 3D structure of myoglobin, showing coloured alpha helices. ...
The current FASTA package contains programs for protein:protein, DNA:DNA, protein:translated DNA (with frameshifts), and ordered or unordered peptide searches. Recent versions of the FASTA package include special translated search algorithms that correctly handle frameshift errors (which six-frame-translated searches do not handle very well) when comparing nucleotide to protein sequence data.
In addition to rapid heuristic search methods, the FASTA package provides SSEARCH, an implementation of the optimal Smith Waterman algorithm. A major focus of the package is the calculation of accurate similarity statistics, so that biologists can judge whether an alignment is likely to have occurred by chance, or whether it can be used to infer homology. The FASTA package is available from ftp.virginia.edu/pub/fasta. The Smith-Waterman algorithm is a well-known algorithm for performing local sequence alignment; that is, for determining similar regions between two nucleotide or protein sequences. ...
In biology, two or more structures are said to be homologous if they are alike because of shared ancestry. ...
The web-interface to submit sequences for running a search of the European Bioinformatics Institue (EBI)'s online databases is also available called fasta33 The European Bioinformatics Institute (EBI) part of EMBL is a centre for research and services in bioinformatics. ...
The FASTA file format used as input for this software is now largely used by other sequence database search tools (such as BLAST) and sequence alignment programs (Clustal, T-Coffee, ...) In bioinformatics, FASTA format is a file format used to exchange information between genetic sequence databases. ...
In bioinformatics, Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences. ...
Clustal is a widely used multiple sequence alignment computer program. ...
T-Coffee is a multiple sequence alignment software using a progressive approach. ...
Search method
Fasta takes a given nucleotide or amino-acid sequence and searches a corresponding sequence database by using local sequence alignment to find matches of similar database sequences. In bioinformatics, a sequence alignment is a way of arranging the primary sequences of DNA, RNA, or protein to identify regions of similarity that may be a consequence of functional, structural, or evolutionary relationships between the sequences. ...
The FASTA program follows a largely heuristic method which contributes to the high speed of its execution. It initially observes the pattern of word hits, word to word matches of a given length, and marks potential matches before performing a more time consuming optimized search using a Smith-Watermann type of algorithm. The size taken for a word, given by the parameter ktup, controls the senstivity and speed of the program. Increasing the ktup value decreases number of background hits that are found. From the word hits that are returned the program looks for segments that contain a cluster of nearby hits. It then investigates these segments for a possible match. The Smith-Waterman algorithm is a well-known algorithm for performing local sequence alignment; that is, for determining similar regions between two nucleotide or protein sequences. ...
There are some differences between fastn and fastp relating to the type of sequences used but both use four steps and calculate three scores to describe and format the sequence similarity results. These are: Image File history File links Download high resolution version (472x655, 14 KB) Summary Inner working of the FASTA program. ...
- Identify regions of highest density in each sequence comparison. Taking a ktup to equal 1 or 2.
- In this step all or a group of the identities between two sequences are found using a look up table. The ktup value determines how many consecutive identities are required for a match to be declared. Thus the lesser the ktup value: the more sensitive the search. ktup=2 is frequently taken by users for protein sequences and ktup=4 or 6 for nucleotide sequences. Short oligonucleotides are usually run with ktup = 1. The program then finds all similar local regions, represented as diagonals of a certain length in a dot plot, between the two sequences by counting ktup matches and penalizing for intervening mismatches. This way, local regions of highest density matches in a diagonal are isolated from background hits. For protein sequences BLOSUM50 values are used for scoring ktup matches. This ensures that groups of identities with high similarity scores contribute more to the local diagonal score than to identities with low similarity scores. Nucleotide sequences use the identity matrix for the same purpose. The best 10 local regions selected from all the diagonals put together are then saved.
- Rescan the regions taken using the scoring matrices. trimming the ends of the region to include only those contributing to the highest score.
- Rescan the 10 regions taken. This time use the relevant scoring matrix while rescoring to allow runs of identities shorter than the ktup value. Also while rescoring conservative replacements that contribute to the similarity score are taken. Though protein sequences use the BLOSUM50 matrix, scoring matrices based on the minimum number of base changes required for a specific replacement, on identities alone, or on an alternative measure of similarity, can also be used with the program. For each of the diagonal regions rescanned this way, a subregion with the maximum score is identified. The initial scores found in step1 are used to rank the library sequences. The highest score is referred to as init1 score.
- In an alignment if several initial regions with scores greater than a CUTOFF value are found, check whether the trimmed initial regions can be joined to form an approximate alignment with gaps. Calculate a similarity score that is the sum of the joined regions penalising for each gap 20 points. This initial similarity score (initn) is used to rank the library sequences. The score of the single best initial region found in step 2 is reported (init1).
- Here the program calculates an optimal alignment of initial regions as a combination of compatible regions with maximal score. This optimal alignment of initial regions can be rapidily calculated using a dynamic programming algorithm. The resulting score initn is used to rank the library sequences.This joining process increases sensitivity but decreases selectivity. A carefully calculated cut-off value is thus used to control where this step is implemented, a value that is approximately one standard deviation above the average score expected from unrelated sequences in the library. A 200-residue query sequence with ktup2 uses a value 28.
- Use a banded Smith-Waterman algorithm to calculate an optimal score for alignment.
- This step uses a banded Smith-Waterman algorithm to create an optimised score (opt) for each alignment of query sequence to a database(library) sequence. It takes a band of 32 residues centered on the init1 region of step2 for calculating the optimal alignment. After all sequences are searched the program plots the initial scores of each database sequence in a histogram, and calculates the statistical significance of the "opt" score. For protein sequences, the final alignment is produced using a full Smith-Waterman alignment. For DNA sequences, a banded alignment is provided.
In bioinformatics, a substitution matrix estimates the rate at which each possible residue in a sequence changes to each other residue over time. ...
In bioinformatics, a substitution matrix estimates the rate at which each possible residue in a sequence changes to each other residue over time. ...
In bioinformatics, a substitution matrix estimates the rate at which each possible residue in a sequence changes to each other residue over time. ...
In probability and statistics, the standard deviation of a probability distribution, random variable, or population or multiset of values is defined as the square root of the variance. ...
The Smith-Waterman algorithm is a well-known algorithm for performing local sequence alignment; that is, for determining similar regions between two nucleotide or protein sequences. ...
The Smith-Waterman algorithm is a well-known algorithm for performing local sequence alignment; that is, for determining similar regions between two nucleotide or protein sequences. ...
In statistics, a histogram is a graphical display of tabulated frequencies. ...
The Smith-Waterman algorithm is a well-known algorithm for performing local sequence alignment; that is, for determining similar regions between two nucleotide or protein sequences. ...
See also In bioinformatics, Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences. ...
In bioinformatics, FASTA format is a file format used to exchange information between genetic sequence databases. ...
In bioinformatics, a sequence alignment is a way of arranging the primary sequences of DNA, RNA, or protein to identify regions of similarity that may be a consequence of functional, structural, or evolutionary relationships between the sequences. ...
This list of sequence alignment software is a compilation of bioinformatics software tools and web portals used in pairwise sequence alignment, multiple sequence alignment, and structural alignment. ...
Sequence profiling Tools in bioinformatics refer to all those software tools (web-based/downloadable) that provide a brief overview on all related information about an input sequence. ...
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