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  2. Probalign - Wikipedia

    en.wikipedia.org/wiki/Probalign

    Probalign is a sequence alignment tool that calculates a maximum expected accuracy alignment using partition function posterior probabilities. [1] Base pair probabilities are estimated using an estimate similar to Boltzmann distribution. The partition function is calculated using a dynamic programming approach.

  3. Sequence alignment - Wikipedia

    en.wikipedia.org/wiki/Sequence_alignment

    Hybrid methods, known as semi-global or "glocal" (short for global-local) methods, search for the best possible partial alignment of the two sequences (in other words, a combination of one or both starts and one or both ends is stated to be aligned). This can be especially useful when the downstream part of one sequence overlaps with the ...

  4. Gap penalty - Wikipedia

    en.wikipedia.org/wiki/Gap_penalty

    Therefore, using a good gap penalty model will avoid low scores in alignments and improve the chances of finding a true alignment. [3] In genetic sequence alignments, gaps are represented as dashes(-) on a protein/DNA sequence alignment. [1] Unix diff function - computes the minimal difference between two files similarly to plagiarism detection.

  5. Smith–Waterman algorithm - Wikipedia

    en.wikipedia.org/wiki/Smith–Waterman_algorithm

    The Smith–Waterman algorithm performs local sequence alignment; that is, for determining similar regions between two strings of nucleic acid sequences or protein sequences. Instead of looking at the entire sequence, the Smith–Waterman algorithm compares segments of all possible lengths and optimizes the similarity measure .

  6. Maximal unique match - Wikipedia

    en.wikipedia.org/wiki/Maximal_unique_match

    A maximal unique match or MUM, for short, is part of a key step [1] in the multiple sequence alignment of genomes in computational biology. Identification of MUMs and other potential anchors is the first step in larger alignment systems such as MUMmer. Anchors are the areas between two genomes where they are highly similar.

  7. Dot plot (bioinformatics) - Wikipedia

    en.wikipedia.org/wiki/Dot_plot_(bioinformatics)

    The main diagonal represents the sequence's alignment with itself; lines off the main diagonal represent similar or repetitive patterns within the sequence. In bioinformatics a dot plot is a graphical method for comparing two biological sequences and identifying regions of close similarity after sequence alignment. It is a type of recurrence plot.

  8. T-Coffee - Wikipedia

    en.wikipedia.org/wiki/T-Coffee

    Two alignment sources are used for each pair of sequences, one of them classified as local, and the other as global. [ 1 ] Global alignments are constructed using Clustal W on the sequences, two at a time, and sed to give one full-length alignment between each pair of sequences.

  9. 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.