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  2. Sequence alignment - Wikipedia

    en.wikipedia.org/wiki/Sequence_alignment

    In bioinformatics, a sequence alignment is a way of arranging the 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. [1] Aligned sequences of nucleotide or amino acid residues are typically represented as rows within a matrix.

  3. MAFFT - Wikipedia

    en.wikipedia.org/wiki/MAFFT

    In bioinformatics, MAFFT (multiple alignment using fast Fourier transform) is a program used to create multiple sequence alignments of amino acid or nucleotide sequences. . Published in 2002, the first version used an algorithm based on progressive alignment, in which the sequences were clustered with the help of the fast Fourier transfo

  4. List of sequence alignment software - Wikipedia

    en.wikipedia.org/wiki/List_of_sequence_alignment...

    This list of sequence alignment software is a compilation of software tools and web portals used in pairwise sequence alignment and multiple ... Bioinformatics. 26 ...

  5. Multiple sequence alignment - Wikipedia

    en.wikipedia.org/wiki/Multiple_sequence_alignment

    Multiple sequence alignment (MSA) is the process or the result of sequence alignment of three or more biological sequences, generally protein, DNA, or RNA. These alignments are used to infer evolutionary relationships via phylogenetic analysis and can highlight homologous features between sequences.

  6. Gap penalty - Wikipedia

    en.wikipedia.org/wiki/Gap_penalty

    Genetic sequence alignment - In bioinformatics, gaps are used to account for genetic mutations occurring from insertions or deletions in the sequence, sometimes referred to as indels. Insertions or deletions can occur due to single mutations, unbalanced crossover in meiosis , slipped strand mispairing , and chromosomal translocation . [ 2 ]

  7. Sequence assembly - Wikipedia

    en.wikipedia.org/wiki/Sequence_assembly

    In bioinformatics, sequence assembly refers to aligning and merging fragments from a longer DNA sequence in order to reconstruct the original sequence. [1] This is needed as DNA sequencing technology might not be able to 'read' whole genomes in one go, but rather reads small pieces of between 20 and 30,000 bases, depending on the technology used. [1]

  8. Bowtie (sequence analysis) - Wikipedia

    en.wikipedia.org/wiki/Bowtie_(sequence_analysis)

    Bowtie is a software package commonly used for sequence alignment and sequence analysis in bioinformatics. [3] The source code for the package is distributed freely and compiled binaries are available for Linux, macOS and Windows platforms. As of 2017, the Genome Biology paper describing the original Bowtie method has been cited more than ...

  9. Bioinformatics - Wikipedia

    en.wikipedia.org/wiki/Bioinformatics

    Sequences of genetic material are frequently used in bioinformatics and are easier to manage using computers than manually. These are sequences being compared in a MUSCLE multiple sequence alignment (MSA). Each sequence name (leftmost column) is from various louse species, while the sequences themselves are in the second column.